All cellular organisms require mechanisms to purge
unwanted or dysfunctional proteins. In eukaryotes, the
autophagy-lysosome and ubiquitin-proteasome systems (UPS) are the two
major quality control pathways responsible for maintaining proteome
homeostasis and directing recycling to meet nutrient demand.
Perhaps unsurprisingly given their widespread influence,
definitive etiological links exist between various human diseases and
mutations in genes that control the UPS and autophagic degradation
routes.
Synthesis
of 26S proteasomes is energetically
costly given their complexity and
abundance and, as a consequence, cells have evolved sophisticated
mechanisms to ensure an adequate supply of functioning particles. In
fact, proteasomes comprise as much as 1% of total protein in certain
mammalian cell types (
Tanaka and Ichihara, 1989).
The main control point is through regulated expression of the
corresponding suite of proteasome subunits and associated genes, which
is tightly co-ordinated in an attempt to provide stoichiometric amounts
of each polypeptide (
Figure 2).
How tight this regulation is within the collection of proteasome genes
remains unclear, as excess subunits do not typically accumulate within
cells as free forms (the exception being Rpn10), and appear to be
rapidly degraded if they fail to integrate into their respective CP or
RP sub-complexes (
Peters et al., 2015;
Nahar et al., 2019).
Thus, while transcription and translation are modulated in an attempt
to provide stoichiometric expression, an important arbiter dictating the
final concentration of proteasomes might be the abundance of one or
more factors in limiting supply. Nevertheless, multiple studies have
documented the concerted transcriptional regulation of proteasome genes
during development or in response to stress, and have contributed to a
growing body of evidence for common signaling pathways regulating their
expression.
Figure 2. Transcriptional Regulation of Proteasome Subunit Genes. (A) Regulation of proteasome gene expression in yeast. Expression of the transcription factor Rpn4 is controlled by various cis-regulatory
elements bound by transcription factors, such as Hsf1, Pdr1, and Yap1.
Rpn4 has an extremely short half-life and is continuously ubiquitylated
and degraded by the 26S proteasome under normal growth conditions, a
pathway initiated by the E2 Rad6 and the E3 Ubr2. A
ubiquitin-independent route for Rpn4 degradation also exists. When
proteasome capacity is exceeded or impaired, Rpn4 is stabilized and
translocates to the nucleus, where it binds to a hexameric consensus
nucleotide sequence [(A/G)GTGGC], known as the proteasome-associated
control element (PACE), present in the promoters of most proteasome
subunit genes. This binding leads to increased expression of proteasome
subunits, along with additional genes involved in protein
ubiquitylation, DNA repair, and other stress responses. One of the
latter genes encodes Yap1, which can further increase Rpn4 levels via a
positive-feedback loop. HSE, heat shock element; YRE, Yap response
element; PDRE, pleiotropic drug response element; aa, amino acids.
(B)
Regulation of proteasome gene expression in mammals and plants. The
mammalian transcription factor NRF1 is a type II endoplasmic reticulum
(ER) membrane protein that is continuously retro-translocated to the
cytosol via the ER-associated protein degradation (ERAD) pathway, a
process requiring activity of the E3 ligase HRD1 and the AAA-ATPase
CDC48/p97. Retro-translocated NRF1 is rapidly ubiquitylated and degraded
by the 26S proteasome.
When proteasome capacity is exceeded or
impaired, NRF1 is stabilized during retro-translocation, where it is
cleaved by the aspartyl protease DDI2. The resulting active form of NRF1
is deglycosylated by PNG1 and then translocates to the nucleus, where
it binds antioxidant response elements (AREs) to activate transcription
of its target genes, including those encoding proteasome subunits. The Arabidopsis
transcription factors NAC53 and NAC78 control proteasome subunit gene
expression and are predicted to be ER-localized transmembrane proteins.
Given that Arabidopsis DDI1 also contains an aspartyl protease
domain, we predict that transcriptional regulation of the proteasome in
plants proceeds by a similar mechanism as in mammalian cells, by which
the processed NAC53/78 dimer enters the nucleus and binds to
proteasome-related cis-elements (PRCEs) to activate transcription.
In yeast, mammals and plants, the
controlled expression of proteasome subunit genes is achieved by the
unrelated but functionally analogous transcription factors Rpn4, NRF1/2,
and NAC53/78, respectively (
Figure 2).
This regulation is best understood in yeast, where the C2H2-type zinc
finger transcription factor Rpn4 binds to a six nucleotide sequence
[(A/G)GTGGC)] known as the proteasome-associated control element (PACE)
that can be found in the promoter region of genes encoding most
proteasome subunits and related factors (
Mannhaupt et al., 1999;
Xie and Varshavsky, 2001;
Shirozu et al., 2015).
Rpn4 has an extremely short half-life due to rapid proteasomal degradation (
Xie and Varshavsky, 2001).
However, when proteasome capacity fails to keep up with demand, Rpn4
turnover slows, leading to a rise in its levels and a concomitant
increase in proteasome gene expression (
Figure 2A). Rpn4 itself is integrated into a broader stress-responsive regulatory network, including controls on
RPN4 gene expression by several transcription factors including Hsf1, Pdr1, Pdr3, and Yap1 (
Figure 2A;
Owsianik et al., 2002;
Hahn et al., 2006).
The proteasomal degradation of Rpn4 under low proteasome
demand is mediated by two distinct degrons, both of which must be
blocked to stabilize Rpn4 (
Ju and Xie, 2004). One degron is independent of ubiquitin (
Ha et al., 2012), while the second relies on phosphorylation-induced ubiquitylation of specific lysines via the E2 Rad6 and the E3 Ubr2 (
Wang et al., 2004;
Ju and Xie, 2006;
Ju et al., 2007).
The ubiquitin-independence of one breakdown route is unusual for a
short-lived protein, but it might ensure that Rpn4 is sensitive
principally to fluctuations in proteasome activity, rather than
ubiquitin availability, which is separately regulated (
Hanna et al., 2007).
Controlling Rpn4 levels and activity, and hence proteasome abundance,
is critical for yeast survival in response to multiple stresses,
including DNA damage, proteotoxic stress, and changes in redox balance (
Wang et al., 2008,
2010a;
Ma and Liu, 2010).
A similar regulatory loop exists in mammalian cells,
where a concerted increase in the expression of proteasome subunits is
observed in response to proteasome inhibition (
Meiners et al., 2003).
However, the lack of obvious mammalian orthologs of Rpn4 and PACE
sequences within proteasome subunit genes suggested early on that
novel
mechanism(s) are in play.
NF-Y dictates the expression of loci encoding six CP subunit (α
2, α
5, α
7, β
3, β
4 and β
6),
five RP subunits (RPT1, RPT5, RPT6, RPN10, and RPN11), and one assembly
chaperone (NAS6/p28), each of which contains one or more CCAAT
cis-elements in their promoter regions (
Xu et al., 2012).
FOXO4 promotes RPN6 expression, which contributes to high proteasome activity in pluripotent stem cells (
Vilchez et al., 2012), while STAT3 regulates the expression of numerous β-subunit genes (
Vangala et al., 2014).
Additionally, two basic leucine zipper family
transcription factors appear to fulfill the role of yeast Rpn4 in
up-regulating proteasome gene expression when capacity is impaired:
nuclear factor erythroid 2-related factor 1 (
NRF1, also known as NFE2L1)
and, to a lesser extent, NRF2 (
Radhakrishnan et al., 2010;
Steffen et al., 2010;
Lee C. S. et al., 2011;
Koizumi et al., 2018).
Chromatin immunoprecipitation (ChIP)-seq experiments identified
(A/G)TGACTCAGC as the consensus binding site for NRF1 in mice (
Baird et al., 2017), which notably exists in the enhancer or promoter regions of all proteasome subunit genes.
Similar to yeast Rpn4, N
RF1 is rapidly degraded by the UPS, albeit via a different mechanism (
Figure 2B).
NRF1 is a type II integral ER membrane protein (Wang and Chan, 2006; Zhang et al., 2007)
that is retro-translocated continuously from the ER back to the cytosol
under normal conditions via the ER-associated protein degradation
(ERAD) pathway, where it is rapidly ubiquitylated and removed by 26S
proteasomes (
Figure 2B;
Steffen et al., 2010;
Radhakrishnan et al., 2014;
Sha and Goldberg, 2014).
This turnover requires ubiquitylation of NRF1 by the ER-resident E3
HRD1(synoviolin) [which also acts as the
retro-translocation channel (
Schoebel et al., 2017)], and subsequent extraction by
Ccd48/p97 (
Steffen et al., 2010;
Radhakrishnan et al., 2014).
When proteasomal capacity is limited, NRF1 stalls during
retro-translocation and is instead deglycosylated and proteolytically
liberated from the ER in an active form that subsequently translocates
into the nucleus to drive transcription (
Figure 2B;
Radhakrishnan et al., 2014;
Sha and Goldberg, 2014;
Lehrbach et al., 2019).
After some initial controversy regarding the identity of the responsible protease (
Sha and Goldberg, 2014,
2016;
Vangala et al., 2016),
it is now clear that this cleavage is performed by the
UBL-UBA protein
DDI2, using the aspartyl protease activity provided by its distinctive
retroviral protease-like domain (
Figure 2B;
Koizumi et al., 2016).
A likely scenario is that this shuttle factor selectively recognizes
ubiquitylated NRF1 through their ubiquitin-binding capacities and then
direct its cleavage. An analogous mechanism exists in
Caenorhabditis elegans (
Lehrbach and Ruvkun, 2016,
2019),
suggesting that this activation mechanism is widely conserved among
animals. Once inside the nucleus, NRF1 stability is additionally
regulated by at least two CRL E3s that trigger its ubiquitylation and
subsequent degradation, with this turnover also sensitive to proteasome
capacity (
Biswas et al., 2011;
Tsuchiya et al., 2011).
In
Arabidopsis, the c
o-ordinated expression of
proteasome subunit genes is controlled by at least two transcription
factors from the NAM/ATAF1/CUC2 (NAC) family, NAC53 and NAC78 (
Yabuta et al., 2011;
Nguyen et al., 2013;
Gladman et al., 2016).
NAC78 (also known as NTL11 or RPX1) was initially identified as a gene
whose expression was up-regulated in response to intense light and heat
stress (
Nishizawa et al., 2006;
Morishita et al., 2009), and whose knock-out increased leaf organ size (
Nguyen et al., 2013).
A role in proteasome gene expression was then identified by
over-expression studies showing that NAC78 positively regulates the
expression of core proteasome subunit genes, and that its putative
DNA-binding site [TGGGC, known as the
proteasome-related cis-
element (PRCE)] is present within many, but not all, associated promoters (
Morishita et al., 2009;
Yabuta et al., 2011;
Nguyen et al., 2013). Interestingly, while many proteasome subunits are encoded by paralogous genes in
Arabidopsis and other plants (
Fu et al., 1998a,
1999;
Shibahara et al., 2002;
Yang et al., 2004;
Book et al., 2010), often only one gene of a pair is responsive to NAC78 over-expression or treatment with proteasome inhibitors (
Gladman et al., 2016),
suggestive of non-redundancy. Besides proteasome genes, an extended
collection of genes encoding proteasome accessory proteins, assembly
chaperones, autophagy components, and detoxifying enzymes are also
included within the
“proteasome stress” regulon, suggesting that plant
cells use an assortment of strategies to combat proteasome insufficiency
besides assembling more particles (
Gladman et al., 2016).
Promoter-binding and phylogenetic analyses identified a
close homolog of NAC78, termed NAC53 (also known as NTL4) that works in
concert (
Gladman et al., 2016).
The two proteins interact, and the elimination of both, but not each
individually, severely impairs up-regulation of the proteasome stress
regulon in response to proteasome inhibition, rendering the double
nac53 nac78 mutant plants hyper-sensitive to CP inhibitors such as MG132 and bortezomib (
Figure 2B).
Given that NAC53 and NAC78 are predicted to possess a C-terminal
transmembrane domain, and that other members of the membrane-bound NAC
family have been reported to use proteolytic release from membrane
stores to regulate their transcriptional activity (
Kim et al., 2007), we predict that a cleavage mechanism similar to that employed to release mammalian NRF1 from membranes operates in plants (
Figure 2B). In support,
Arabidopsis harbors a homolog of DDI2 (
Farmer et al., 2010)
that could use its internal retroviral protease domain to cleave NAC53
and NAC78, thus permitting their release from the ER and entry into the
nucleus where they would then activate the proteasome stress regulon (
Figure 2B).
Regulated Assembly of the Proteasome Core Protease
Assembly of the holo-26S proteasome following subunit
synthesis is a highly complex process that requires numerous dedicated
chaperones and maturation factors (
Figure 3;
Howell et al., 2017;
Rousseau and Bertolotti, 2018).
Construction of the CP and the Rpt ring of the RP are particularly
challenging as compared to their bacterial and archeal counterparts, due
to diversification of the α, β and Rpt subunits. This heterogeneity
imposes positional constraints on the ordered assembly of the
corresponding
α and β heptameric rings and the
Rpt hexameric ring, and
subsequent docking of these rings in correct register with each other.
As such,
proteasome assembly is a relatively slow process, with an
experimentally determined half-time of around 20 min in yeast (
Chen and Hochstrasser, 1996), and between 30 and 80 min in mammalian cells (
Yang et al., 1995;
Heink et al., 2005;
Hirano et al., 2005).
Because the individual subunits of the α, β and Rpt rings share
substantial sequence and structural similarity, having likely evolved
from a common ancestor (Gille et al., 2003),
mis-assembly can and does occur, leading to faulty assembly
intermediates that sterically occlude or otherwise interfere with
construction and/or activity of the CP and/or RP (
Gerards et al., 1997,
1998;
Yao et al., 1999;
Takeuchi and Tamura, 2004;
Ishii et al., 2015).
Thus, mechanisms to limit the formation of these dysfunctional
products, and remove any that arise inadvertently, are essential for
maintaining a healthy proteasome pool.
Figure 3. Assembly Pathway for 26S Proteasomes in
Yeast. Formation of the CP begins with assembly of the α-subunit ring,
which is mediated by two hetero-dimeric chaperone complexes, Pba1-Pba2
and Pba3-Pba4. Upon α-ring completion, the CP β-subunits are
incorporated in a specific order, starting with β2 followed by β3, β4, β5, β6 and β1,
resulting in sequential formation of 13S, 15S and half-proteasome
intermediates. Assembly of the β-ring is assisted by the Ump1 chaperone,
and the resulting half-proteasome is capped by Blm10. The β7
subunit is then incorporated, which promotes the association of two
half-proteasomes to generate a complete CP. Auto-catalytic removal of
the β-subunit propeptides then activates the CP and leads to Ump1
degradation. The RP base assembles from three separate chaperone
modules, namely Nas2-Rpt4-Rpt5, Nas6-Rpt3-Rpt6-Rpn14, and
Hsm3-Rpt1-Rpt2-Rpn1. These modules associate with one another in an
ordered manner to construct the Rpt ring, followed by incorporation of
Rpn2, Rpn13, and finally Rpn10 to form the completed base. The RP lid
assembles largely spontaneously, beginning with dimerization of Rpn8 and
Rpn11, followed by sequential recruitment of Rpn6, Rpn5, Rpn9, a
trimeric Rpn3-Rpn7-Sem1 complex, and finally, Rpn12. The lid and base
then combine to form a complete RP. Upon completion of CP and RP
assembly, the two sub-complexes associate to form the mature 26S
holo-proteasome. This association occurs via insertion of C-terminal
HbYX motifs from the Rpt subunits into pockets between adjacent CP
α-subunits. Finally, correct CP-RP association is confirmed by an
Ecm29-mediated checkpoint.
CP assembly begins with formation of individual α-rings (Hirano et al., 2008), which then provide a platform onto which the β-subunits incorporate (
Figure 3;
Frentzel et al., 1994;
Nandi et al., 1997;
Schmidtke et al., 1997).
Initial assembly of the α-ring is controlled by two hetero-dimeric
chaperones, termed Pba1-Pba2 and Pba3-Pba4 in yeast, and PAC1-PAC2 and
PAC3-PAC4 in mammals, that provide scaffolds upon which the α-rings are
built (
Hirano et al., 2005;
Kock et al., 2015;
Wani et al., 2015). Pba1-Pba2 can associate with individual α-subunits
in vitro and
in vivo to initiate α-ring formation (
Hirano et al., 2005;
Le Tallec et al., 2007).
Both chaperone subunits also contain a HbYX motif that allows them to
bind and stabilize adjacent α-subunits as they associate (
Kusmierczyk et al., 2011). The HbYX motif of Pba1 inserts into a pocket formed at the α
5-α
6 subunit interface, whereas that of Pba2 inserts at the α
6-α
7 interface, which together likely generate an α
5-α
6-α
7 trimer (
Kusmierczyk et al., 2011). How the α
1, α
2, α
3 and α
4
subunits are subsequently integrated is unknown, but a role for the
Pba3-Pba4 chaperone is likely (see below). Although still viable, yeast
cells lacking Pba1-Pba2 accumulate immature CP species containing
structurally unstable α-rings, from which α
5 and α
6 readily dissociate (
Wani et al., 2015), while mammalian cells with reduced levels of PAC1-PAC2 accumulate fewer complete α-rings (
Hirano et al., 2005).
Through binding to the pockets between the α
5, α
6 and α
7 subunits, Pba1-Pba2 also prevents premature association of CP assembly intermediates with the RP or other activating factors (
Stadtmueller et al., 2012). In mature 26S proteasomes, one of the α
5-α
6 or α
6-α
7 pockets is occupied by the HbYX motif of Rpt5 (
Tian et al., 2011;
Beck et al., 2012;
Schweitzer et al., 2016). Because Pba1-Pba2 appears to have a much higher affinity for α
5-α
6-α
7
present in the CP intermediates as compared to those in the mature CP,
they can outcompete Rpt5 and the rest of the RP for binding until the
α-ring matures (
Wani et al., 2015).
It remains unclear what causes this affinity switch of Pba1-Pba2 for
the α-ring, but allosteric effects caused by processing of the β-subunit
propeptides, or steric alterations in the sizes of the α-ring pore and
HbYX-binding pockets, might be involved (
Kusmierczyk et al., 2011;
Stadtmueller et al., 2012;
Kock et al., 2015;
Wani et al., 2015).
The Pba3-Pba4 heterodimer also participates in the early stages of α-ring assembly (
Hirano et al., 2006,
2008;
Le Tallec et al., 2007;
Yashiroda et al., 2008). It binds tightly to the surface of the α
5 subunit that faces the β-subunits (
Kusmierczyk et al., 2008;
Yashiroda et al., 2008), and is thus displaced from the ring by incoming β
4 (
Figure 3;
Hirano et al., 2008).
Pba3-Pba4 has a unique role among assembly chaperones in that it
ensures formation of canonical 20S proteasomes in which each α-subunit
is present in its correct position (
Kusmierczyk et al., 2008). In the absence of Pba3-Pba4, aberrant α-subunit rings accumulate, containing an invariant α
5-α
6-α
7-α
1 hetero-tetramer, plus various arrangements of α
2, α
3 and α
4 (
Velichutina et al., 2004;
Kusmierczyk et al., 2008;
Takagi et al., 2014;
Padmanabhan et al., 2016).
Only in the presence of Pba3-Pba4 are all seven α-subunits integrated
in correct register, thus generating a uniform CP architecture.
Upon completion, the α-ring provides a platform for assembling the β-ring, formation of which starts with β
2, followed by sequential incorporation of the β
3, β
4, β
5, β
6 and β
1 subunits (
Figure 3). Entry of the “early” β subunits β
2, β
3 and β
4 creates a semi-stable 13S intermediate (
Li et al., 2007;
Hirano et al., 2008), while subsequent entry of β
5, β
6 and β
1 gives rise to a semi-stable 15S intermediate (
Li et al., 2007;
Hirano et al., 2008). In both yeast and mammals, β
7 is the last β-subunit to integrate (
Marques et al., 2007;
Hirano et al., 2008;
Li et al., 2016), leading to a transient species called the “half-proteasome.” Most β-subunits, excluding β
3 and β
4,
are synthesized as precursors bearing an N-terminal propeptide, which
helps with ring assembly and is then removed in mature particles. For
example, the propeptides in β
2 and β
5 are essential for recruiting and incorporating β
3 and β
6, respectively, into the β ring (
Chen and Hochstrasser, 1996;
Hirano et al., 2008). For β
1, β
2, and β
5,
it is also critical that these extensions be removed to expose their
N-terminal catalytic threonine residues that are essential for peptide
bond cleavage (
Chen and Hochstrasser, 1996;
Schmidtke et al., 1996;
Seemuller et al., 1996;
Huber et al., 2016;
Li et al., 2016).
Construction of the β-ring is also aided by binding of
the Ump1 chaperone at the center of the α-ring prior to or concomitant
with β
2 binding (
Figure 3;
Ramos et al., 1998;
Sá-Moura et al., 2013). Yeast lacking the intrinsically disordered Ump1 accumulate CP precursors, arguing that it plays a positive role in assembly (
Ramos et al., 1998).
However, genetic studies have implied a negative role, specifically by
preventing premature dimerization of partially assembled α/β-ring
precursors until a complete 15S half-proteasome is formed (
Li et al., 2007). The N-terminal third of Ump1, which is dispensable for CP binding (
Burri et al., 2000), performs this checkpoint function. The proximity of this region to β
6 ideally positions Ump1 to both block dimerization and sense the arrival of β
7 as the final subunit to be incorporated (
Kock et al., 2015).
Integration of β7 promotes dimerization of two half-proteasomes by insertion of its C-terminal tail into a groove
between β1 and β2 in the opposite β-ring (Figure 3). Following this coupling, the propeptides of β1, β2 and β5
undergo auto-catalytic cleavage to expose their N-terminal catalytic
threonine. These active sites then proteolytically trim the neighboring
propeptides of β
6 and β
7 (
Chen and Hochstrasser, 1996;
Schmidtke et al., 1996;
Seemuller et al., 1996;
Huber et al., 2016;
Li et al., 2016).
Ump1 remains bound through half-proteasome dimerization and β-subunit
processing and ultimately becomes trapped inside the CP when assembly is
complete. It is then degraded by the nascent β-subunit active sites,
thus becoming the first substrate of each proteasome (
Ramos et al., 1998;
Burri et al., 2000;
Griffin et al., 2000;
Li et al., 2007;
Hirano et al., 2008).
Finally, the CP is transiently capped with Blm10 (known
as
PA200 in plants and humans). This >200 kDa HEAT-repeat protein
forms a dome on top of the CP (
Schmidt et al., 2005;
Sadre-Bazzaz et al., 2010) using its C-terminal HbYX motif for α-ring docking (
Dange et al., 2011). Blm10 likely confers increased stability to the CP (
Li et al., 2007;
Lehmann et al., 2008). For example, when deletion of the β
7 tail is combined with deletion of the
BLM10 gene, yeast cells exhibit a severe CP assembly defect (
Marques et al., 2007). Additional functions have been ascribed to Blm10, including the potential to block entry of substrates into the CP lumen (
Sadre-Bazzaz et al., 2010;
Dange et al., 2011),
promote CP import into the nucleus (
Weberruss et al., 2013), and
deliver dissociated CP into cytoplasmic proteasome storage granules (PSGs) in response to metabolic stress (
Weberruss et al., 2013;
Marshall and Vierstra, 2018b). In addition,
CP-Blm10 complexes are particularly abundant upon treatment of cells with proteasome inhibitors (
Marshall et al., 2015;
Welk et al., 2016).
Although the function(s) of these particles remain unknown, the
association of Blm10 with the CP could reflect accelerated assembly of
26S proteasomes during such proteotoxic stress.
Although a
ssembly of immuno- and thymo-proteasomes
proceeds in a similar step-wise manner, the three catalytic subunits
(LMP2, MECL1 and LMP7/PSMB11) are co-operatively and preferentially
incorporated in place of their constitutive counterparts (β
1, β
2, and β
5,
respectively). One notable difference is that LMP2 enters the
immuno-proteasome assembly pathway much earlier than for standard
proteasomes, where β
1 is typically the penultimate subunit to be incorporated (
Li et al., 2007;
Hirano et al., 2008). An intermediate complex is formed containing an α-ring, LMP2, MECL1, β
3 and β
4 (
Nandi et al., 1997), with LMP2 and MECL1 being incorporated simultaneously in a mutually dependent manner (
Groettrup et al., 1997;
Griffin et al., 1998;
Kingsbury et al., 2000). LMP7 is then recruited preferentially over β
5 into LMP2- and MECL1-containing intermediates (
Griffin et al., 1998;
Kingsbury et al., 2000). LMP7 binds more tightly to POMP/UMP1 than β
5, and can incorporate independently of β
4 (
Bai et al., 2014),
both of which promote immuno-proteasome assembly. The inter-dependency
of LMP2 and MECL1 incorporation typically results in assembly of
homogenous immuno- and thymo-proteasomes that contain all three
inducible subunits (
Kingsbury et al., 2000).
These variants amass approximately four times faster than standard proteasomes (
Heink et al., 2005), enabling a rapid response to immune and inflammatory stimuli.
Regulated Assembly of the Proteasome Regulatory Particle
Unlike the CP, which is composed entirely of ring
structures, the RP is more architecturally heterogeneous, with the base
and lid sub-complexes assembling independently of each other (
Lander et al., 2012;
Beckwith et al., 2013;
Tomko and Hochstrasser, 2014;
Tomko et al., 2015).
As with the CP, the
RP base depends heavily on dedicated assembly
chaperones for correct positioning for the six members of the Rpt ring (
Figure 3).
Thus far, four Rpt chaperones have been described: Nas2, Nas6, Hsm3 and
Rpn14 in yeast, known as p27, p28, S5b, and PAAF1, respectively, in
mammals (
Funakoshi et al., 2009;
Kaneko et al., 2009;
Le Tallec et al., 2009;
Park et al., 2009;
Roelofs et al., 2009;
Saeki et al., 2009).
These chaperones are unrelated in sequence and independently bind to
the C-terminal domain of a distinct Rpt subunit, resulting in the
formation of three precursor assembly modules: Nas2-Rpt4-Rpt5,
Nas6-Rpt3-Rpt6-Rpn14, and Hsm3-Rpt1-Rpt2-Rpn1 (
Figure 3;
Lee S. Y. et al., 2011;
Barrault et al., 2012;
Takagi et al., 2012;
Park et al., 2013;
Satoh et al., 2014). These modules are stabilized in part by the intertwining N-terminal coiled-coil regions of the Rpt subunit pairs (
Zhang et al., 2009), which at least for one pair (Rpt1-Rpt2) is thought to begin co-translationally (
Panasenko et al., 2019).
As described below, the Nas2 and Nas6 modules first associate with each
another, followed by incorporation of the Hsm3 module, along with Rpn2
and Rpn13. Rpn10 is then recruited to complete assembly of the RP base. A
checkpoint involving ubiquitylation of Rpt5 by the RING E3 Not4 helps
ensure that the chaperone-bound modules are integrated in the correct
order (
Fu et al., 2018).
Currently, two mutually non-exclusive routes for base
assembly have been proposed; in the first, the base assembles alone,
whereas in the second, base assembly is templated by the CP. The first
model is supported in yeast by the detection of fully-constructed base
sub-complexes containing assembly chaperones, coupled with the absence
of these chaperones in holo-26S proteasomes (
Kriegenburg et al., 2008;
Funakoshi et al., 2009;
Le Tallec et al., 2009;
Park et al., 2009;
Roelofs et al., 2009;
Saeki et al., 2009).
Immunoprecipitation experiments then showed that Nas2 readily
co-purifies with all components of the Nas2 and Nas6/Rpn14 modules, but
not with components of either the Hsm3 module, lid, or CP (
Tomko et al., 2010). An analogous stepwise incorporation was inferred in mammalian cells (
Kaneko et al., 2009),
although the Nas2 module, rather than the Hsm3 module, was proposed to
be the last to enter the emerging RP base. Fully constructed base
sub-complexes complete with chaperones could also be achieved in
E. coli by co-expressing the nine base subunits along with the four constitutive base assembly chaperones (
Beckwith et al., 2013). As
E. coli
is devoid of proteasomes and associated proteins, this recombinant
system defined the minimal environment for base assembly and provided
unequivocal evidence that the RP base can self-organize independently of
the CP and RP lid.
In the templated model of base assembly, base modules
are delivered to the CP and connected directly on the surface of the CP
α-ring. This model originated from the detection of base assembly
intermediates associated with the CP when the α-ring was compromised (
Kusmierczyk et al., 2008).
Additionally, C-terminal truncations of Rpt4 and Rpt6 created strong
base assembly defects, suggesting that
docking of the C-terminal HbYX
motifs in these subunits onto the CP is critical for base assembly in vivo (
Park et al., 2009).
Both models agree that
chaperones must dissociate from the assembled
base to properly dock the RP onto the CP to then trigger gate opening.
The base appears to exploit ATP-dependent conformational changes in the
Rpt subunits to evict the chaperones and allow stable RP-CP association (Roelofs et al., 2009; Park et al., 2013). This mechanism was recently described in detail for Nas6 (Nemec et al., 2019);
upon lid-base association, interaction of Rpn5 with the base promotes
an ATP-dependent conformational change in Rpt3 that drives release of
Nas6 from the nascent proteasome.
Recently,
Adc17 was identified as an adaptive proteasome
assembly chaperone that regulates the Nas6-Rpt3-Rpt6-Rpn14 module in
yeast (
Hanssum et al., 2014).
Adc17 associates with the N-terminal domain of Rpt6 and appears to
promote Rpt3-Rpt6 dimerization, which in turn enhances proteasome
assembly under conditions that elicit proteotoxic stress. Expression of
Adc17 is induced under these conditions via a mechanism independent of
Rpn4 but regulated by the central stress and autophagy regulator Tor1/2 (
Hanssum et al., 2014).
Pharmacological or genetic inhibition of Tor1/2 enhances expression of
Adc17 (and other proteasome assembly chaperones) via the
mitogen-activated protein kinase Mpk1 (ERK5/MAPK7 in mammals;
Rousseau and Bertolotti, 2016), thus representing
a novel route for up-regulating 26S proteasome assembly when its capacity is exceeded.
Co-expression studies imply that
RP lid biogenesis begins with dimerization of Rpn8 and Rpn11, followed by recruitment of Rpn6 (
Estrin et al., 2013), which then conscripts Rpn5 and Rpn9 to the particle (
Sharon et al., 2006). In parallel, Rpn3 and Rpn7 are brought together by Sem1 to form a hetero-trimeric complex (
Figure 3;
Fukunaga et al., 2010;
Tomko and Hochstrasser, 2011,
2014).
These two sub-complexes then combine to create a nearly complete lid
intermediate that lacks only
Rpn12, which becomes the final subunit to
associate (
Fukunaga et al., 2010;
Tomko and Hochstrasser, 2011;
Tomko et al., 2015).
While no assembly chaperones have yet been identified for the RP lid,
the unusual proteasome subunit Sem1 likely plays a critical role (
Tomko and Hochstrasser, 2014).
Sem1 escaped detection for many years because of its small size,
near-complete lack of secondary and tertiary structure, and an absence
of lysine residues that challenged its detection by proteomic methods (
Russell et al., 2013;
Kragelund et al., 2016).
Well-resolved cryo-EM views have since shown that it binds to a
hydrophobic pocket between Rpn3 and Rpn7 to stabilize an otherwise weak
interaction during the early stages of lid biogenesis (
Wei et al., 2008;
Tomko and Hochstrasser, 2014;
Dambacher et al., 2016).
It is also becoming clear that Rpn12 is pivotal to lid maturation by inducing several conformational changes upon integration (
Estrin et al., 2013;
Tomko et al., 2015).
The RP intermediate lacking Rpn12 adopts a more compact state as
compared to that found in the complete RP and, surprisingly,
introduction of just the C-terminal α-helix of Rpn12 is sufficient to
drive this large-scale conformational re-organization (
Tomko et al., 2015).
The Rpn12 α-helix sits centrally within a helical bundle created by
clustering of the C-termini of most Rpn subunits, and thus might be
responsible for “sensing” the assembly state of the lid.
The
Rpn8-Rpn11 deubiquitylating module also undergoes a conformational change during lid maturation (
Dambacher et al., 2016).
In the isolated lid, this module is positioned perpendicular to its
orientation in the holo-proteasome, which is likely incompatible with
base binding and, importantly, might auto-inhibit the deubiquitylating
activity of Rpn11 until RP assembly is complete (
Tomko et al., 2015;
Dambacher et al., 2016).
It also remains possible that additional motions beyond those involving
Rpn12 and Rpn8-Rpn11 are necessary for the lid-base connection.
The final step in 26S proteasome assembly is association of the RP with the CP (
Figure 3).
Binding is driven by docking of the C-terminal HbYX motifs from several
Rpt ring subunits into pockets between adjacent CP α-subunits, which
also promotes gate opening and substrate entry into the CP lumen (
Smith et al., 2005,
2007;
Rabl et al., 2008;
Tian et al., 2011;
Park et al., 2013). This association occurs spontaneously
in vitro (
Liu et al., 2006;
Livnat-Levanon et al., 2014), is stabilized by ATP (
Smith et al., 2005;
Liu et al., 2006), and is fully reversible (
Bajorek et al., 2003;
Kleijnen et al., 2007;
Wang et al., 2010b;
Marshall and Vierstra, 2018b). Rpn6 is thought to help tether the RP to the CP through binding to the α
2 subunit (
Lander et al., 2012;
Pathare et al., 2012).
Several additional factors have also been implicated, includin
g Ecm29,
which appears to provide a critical quality control checkpoint by
binding to structurally aberrant proteasomes and repressing both the
ATPase activity of the RP and gate opening of the CP in these particles (
Lehmann et al., 2010;
Lee S. Y. et al., 2011;
Panasenko and Collart, 2011;
Park et al., 2011;
De La Mota-Peynado et al., 2013;
Wang et al., 2017).
Hsp90 has also been implicated in CP-RP assembly (
Imai et al., 2003;
Yamano et al., 2008), but its precise role(s) remain unclear.
At present, there is only a rudimentary understanding of 26S proteasome assembly in plants. Proteasome preparations from
Arabidopsis
routinely contain free CP, RP, and singly- and doubly-capped 26S
particles, along with a definitive relative of Blm10 (PA200) connected
to the CP (
Yang et al., 2004;
Book et al., 2010).
Mutants eliminating PA200 do not display defects in phenotype,
ubiquitin conjugate accumulation, proteasome activity, or sensitivity to
proteasome inhibitors (
Book et al., 2010).
However,
a role for PA200 in proteasome regulation is inferred by its
ability to bind
to the CP under conditions that induce proteotoxic
stress (
Book et al., 2010;
Marshall et al., 2015), like its mammalian counterpart (
Welk et al., 2016).
PA200 is also essential for the entry of free
CPs into PSGs during
fixed-carbon starvation, and thus has a role in proteasome storage (
Marshall and Vierstra, 2018b;
see below). Possible orthologs of the yeast assembly chaperones, Pba1,
Pba2, Pba3, Pba4, Ump1, Nas2, Nas6, Hsm3, and Ecm29 have also been
detected in plants, but their amino acid sequence similarities are
sufficiently low to prevent conclusive assignments (D. C. Gemperline, R.
S. Marshall, and R. D. Vierstra, unpublished data). However, the
expression of most, if not all, of these putative chaperones is
up-regulated upon proteasome inhibition in
Arabidopsis (
Gladman et al., 2016), as might be expected for factors needed to assemble proteasomes when supply is limited.
Subcellular Localization of 26S Proteasomes
Fully assembled 26S proteasomes are not static entities,
but instead exhibit
dynamic behavior by
dissociating into free RP and CP
sub-particles, shuttling between the cytoplasm and nucleus, and
re-locating between compartments in response to different growth,
development or environmental challenges. When tagged with GFP, most
proteasome subunits fully incorporate into their appropriate
sub-complexes, thus enabling live cell imaging of the CP, RP, and/or
holo-26S particles. Using these reporters in yeast, mammals and plants,
it is evident that the CP and RP are diffusely spread throughout both
the cytosol and
nucleus, though often substantially enriched in the
latter compartment (
Figure 4A;
Reits et al., 1997;
Enenkel et al., 1998;
Russell et al., 1999;
Brooks et al., 2000;
Pack et al., 2014;
Marshall et al., 2015). Measurements of proteasome activity in the two compartments have varied greatly (
Gardner et al., 2005;
Chen and Madura, 2014;
Dang et al., 2016). Numerous studies, including recent cryo-electron tomographic imaging in the green alga
Chlamydomonas reinhardtii,
found that proteasomes are not distributed evenly within the nucleus,
but instead
accumulate at the inner nuclear membrane,
in the vicinity of
nuclear pore complexes (
Enenkel et al., 1998;
Takeda and Yanagida, 2005;
Albert et al., 2017).
Figure 4. Intracellular Localization of 26S Proteasomes in
Arabidopsis and Yeast. The location of proteasomes was tracked by tagging proteasome subunits with GFP, which allows
in vivo detection via confocal fluorescence microscopy
(A–E),
and a quantitative assay for proteaphagy by measuring the release of
free GFP from the tagged subunits upon entry into vacuoles
(F). (A) 26S proteasomes are found in the cytosol and nucleus of
Arabidopsis
and yeast cells grown in nutrient-rich conditions. Shown is
localization of the PAG1-GFP protein in root tip cells of a 7-day-old
Arabidopsis
seedling (left), or the Pre10-GFP or Rpn5-GFP proteins in exponential
phase yeast cells (top right and bottom right, respectively). Scale
bars, 25 μm (left) and 1 μm (right).
(B) Yeast 26S
proteasomes localize into IPOD-like structures upon inhibition, but to
PSGs upon carbon starvation. Cells expressing Pre10-GFP and the IPOD
marker Rnq1-mCherry were grown in nutrient-rich medium then switched to
either medium containing 80 μM MG132 (top) or medium lacking carbon
(bottom) for 8 h and imaged by confocal fluorescence microscopy. Scale
bar, 1 μm.
(C) Yeast 26S proteasomes are delivered to
the vacuole upon nitrogen starvation but sequester into cytoplasmic PSGs
upon carbon starvation in yeast. Cells expressing Pre10-GFP were grown
in nutrient-rich medium, switched to medium lacking either nitrogen or
carbon for 8 h, and then imaged by confocal fluorescence microscopy.
Scale bar, 1 μm.
(D) 26S proteasomes are sequestered into cytoplasmic PSGs upon fixed carbon starvation in
Arabidopsis. 7-day-old
Arabidopsis
seedlings expressing PAG1-GFP were grown in the light in
sucrose-containing medium and then switched to growth in the dark in
sucrose-free medium for 16 h. Root cells of the lower elongation zone
were imaged by confocal fluorescence microscopy. Scale bar, 10 μm.
(E) Arabidopsis
26S proteasomes are sequestered in autophagic bodies inside vacuoles
upon nitrogen starvation. Seedlings expressing PAG1-GFP or RPN5a-GFP
were grown on nutrient-rich medium and then switched to growth on
nitrogen-free medium plus 1 μM concanamycin A for 16 h. Root cells of
the lower elongation zone were imaged by confocal fluorescence
microscopy. Scale bar, 10 μm.
(F) Time course for the
autophagy-mediated release of free GFP from Pre10-GFP upon nitrogen
starvation in yeast. Wild-type (WT) or autophagy-defective Δ
atg7, Δ
atg10, or Δ
atg13
cells expressing Pre10-GFP were grown in nutrient-rich medium then
switched to medium lacking nitrogen for the indicated times (left panel)
or 8 h (right panel). Total protein extracts were then assayed for
accumulation of free GFP by immunoblot analysis with anti-GFP
antibodies. Open and closed arrowheads locate the Pre10-GFP fusion and
free GFP, respectively. Immunodetection of histone H3 was used to
confirm near-equal protein loading. In panels
(A–E); N,
nucleus; V, vacuole; IPOD, insoluble protein deposit;
PSG, proteasome
storage granule. Images were adapted with permission from
Marshall et al. (2015,
2016) and
Marshall and Vierstra (2018b).
Fluorescence correlation
spectroscopy determined the absolute concentration of the 26S proteasome
in actively dividing yeast cells to be 830–980 nM in the nucleus but
only 140–200 nM in the cytoplasm (
Pack et al., 2014), with similar concentrations observed in cultured mammalian neuronal cells (
Asano et al., 2015).
However, proteasome concentration can be much higher in localized areas
at the inner nuclear membrane, being recorded at over 8 μM in
C. reinhardtii (
Albert et al., 2017).
By contrast, proteasomes in quiescent cells are exported from the
nucleus and sequestered into reversible, motile cytoplasmic PSGs that
collectively reflect a rapid and dramatic re-localization of 26S
proteasomes out of the nucleus, presumably for storage (
Figures 4B–
D;
Bingol and Schuman, 2006;
Laporte et al., 2008;
Yedidi et al., 2016;
Gu et al., 2017;
Marshall and Vierstra, 2018b).
Re-feeding with a fresh carbon source immediately reverses this process
by stimulating rapid import of the RP and CP sub-particles back into
the nucleus followed by holo-26S proteasome assembly. While not found in
granules,
aged proteasomes (over 3 days old) were similarly found to be
largely
cytosolic in mouse embryonic fibroblasts (
Tomita et al., 2019).
Given the sheer size of 26S proteasomes and their RP and
CP sub-particles,
a major challenge to cells during proteasome
re-localization is the transport of these particles into and out of the
nucleus through their size-limited nuclear pores (
Beck and Hurt, 2017).
In proliferating yeast, proteasomes are
imported into the nucleus as CP
and RP assembly intermediates, each of which bears one or more
nuclear
localization signals (NLS;
Tanaka et al., 1990;
Nederlof et al., 1995).
The
NLS is recognized by an importin-α/β heterodimer assembled from two
members of the β-karyopherin family, termed Srp1/Kap60 and Kap95,
respectively (
Enenkel et al., 1995).
Given that only a small number of proteasome subunits contain an NLS,
it was originally speculated that yeast proteasomes enter the nucleus as
separate CP, RP lid and RP base sub-complexes (
Lehmann et al., 2002;
Wendler et al., 2004;
Isono et al., 2007).
However, several studies subsequently implied that the
final steps of
CP assembly occur in the nucleus after
importin-α/β dependent transport.
For example, co-immunoprecipitation studies with Srp1 detected its
association with CP assembly intermediates but not with the mature CP,
as reflected by the presence of unprocessed β
5 subunit propeptides (
Lehmann et al., 2002).
Additionally, yeast CP assembly intermediates accumulate in the nucleus
when their maturation is suppressed by deletion of Ump1 (
Lehmann et al., 2002).
The CP has been proposed to exist in import-competent
and import-incompetent configurations, depending on
accessibility of the
NLS within specific α-subunits (
Tanaka et al., 1990).
Recent cryo-EM structures support this hypothesis by showing that NLS
sequences in the CP are exposed in assembly intermediates due to
disorder within the α-rings (
Kock et al., 2015;
Wani et al., 2015),
but are masked in more mature particles due to conformational changes
that close the α-rings and permit RP binding. In a similar fashion, the
RP base appears to be imported by itself into the nucleus using an NLS
within the Rpt2 or Rpn2 subunits that binds importin-α/β (
Wendler et al., 2004;
Isono et al., 2007;
Savulescu et al., 2011;
Weberruss et al., 2013).
Blm10, a protein structurally related to Rpn2, also facilitates nuclear
import of mature CP upon resorption of PSGs, when quiescent cells
resume growth following periods of starvation (
Weberruss et al., 2013).
A collection of studies also indicate that entire holo-proteasomes can undergo nuclear translocation without disassembly (
Reits et al., 1997;
Chen et al., 2011;
Savulescu et al., 2011;
Pack et al., 2014).
This should be possible given that the channel of the nuclear pore
complex can expand to accommodate cargo with a diameter of up to 39 nm (
Pante and Kann, 2002), although the mechanism by which this might occur remains obscure (
Burcoglu et al., 2015). The most convincing evidence comes from a genetically stabilized 26S proteasome in which the α
4
subunit of the CP was translationally fused to the Rpt1 or Rpt2
subunits of the RP, thus blocking CP-RP dissociation. Surprisingly,
these 26S proteasomes did not exhibit obvious structural defects and
were distributed normally in the nucleus, even upon exit of cells from
stationary phase when cytosolic PSGs dissolve and the levels of nuclear
proteasomes returned back to normal (
Laporte et al., 2008;
Pack et al., 2014).
Since protein synthesis is stalled during quiescence, CP precursors
were not available for import, leading to the conclusion that a nuclear
import pathway exists that makes use of the older, mature, stabilized
complexes (
Pack et al., 2014).
As will be described below, nuclear 26S proteasomes also become
substrates of autophagy following nitrogen starvation or inactivation,
which
a priori requires export from the nucleus. A current model
posits that 26S particles dissociate into free, stable CP and RP
sub-complexes, which are then separately exported (
Nemec et al., 2017).
In addition to nuclear and cytoplasmic proteasomes, a
plasma membrane-localized form of the CP was recently described in
mammalian neurons (
Ramachandran and Margolis, 2017).
This novel CP is exposed to the cell surface, and appears to
exclusively degrade ribosome-associated nascent polypeptides in a
ubiquitin-independent manner upon their synthesis after neuronal
stimulation (
Ramachandran et al., 2018).
An intriguing possibility is that
these bound proteasomes directly
extrude peptides out of the cell
to attenuate neuronal activity-induced
calcium signaling (
Ramachandran and Margolis, 2017). Whether such membrane-associated proteasomes exist in other organisms or cell types remains to be determined.
Proteasome Regulation by Post-Translational Modification
Post-translational modifications of 26S proteasomes
offer additional opportunities to influence proteasome assembly,
activity, localization and abundance. Thus far, over 350 sites of
post-translational modification have been identified on the 26S
particle, which include acetylation, ADP-ribosylation, glycosylation,
methylation, myristoylation, oxidation, phosphorylation, SUMOylation,
ubiquitylation, and proteolytic processing (
Kikuchi et al., 2010;
Cui et al., 2014;
Hirano et al., 2016).
In fact, the same proteasome site might be targeted by more than one
modification, suggesting cross-talk between different types (
Zong et al., 2014). Unfortunately, the functional consequences for most of these alterations are currently unclear.
One common modification is phosphorylation, which
affects almost all proteasome subunits and is directed by an assortment
of proteasome-interacting kinases and phosphatases (
Iwafune et al., 2002;
Lu et al., 2008;
Kikuchi et al., 2010).
As an example of the importance of phosphorylation, treatment of
purified mammalian proteasomes with alkaline phosphatase leads to
dissociation of the CP and RP (
Satoh et al., 2001).
Phosphorylation of Ser-120 in RPT6 by protein kinase A (PKA), and its
dephosphorylation by protein phosphatase 1γ (PP1γ), likely regulates the
interaction between RPT6 and the α
2 subunit of the CP to effect this dissociation (
Satoh et al., 2001;
Asai et al., 2009).
Ser-14 of RPN6 also becomes phosphorylated by PKA, which leads to
increased levels of doubly-capped proteasomes, thus stimulating overall
protein degradation rates (
Lokireddy et al., 2015), consistent with the proposed role for RPN6 in mediating CP-RP association (
Lander et al., 2012;
Pathare et al., 2012).
Another example is the phosphatase UBLCP1, which binds to RPN1 via a
UBL domain and subsequently dephosphorylates RPT1. This modification
regulates nuclear proteasome assembly, again by controlling association
of the RP and CP (
Guo et al., 2011;
Sun et al., 2017). The interaction of Ecm29 with the proteasome is similarly regulated by phosphorylation of the CP subunit α
7 (
Wani et al., 2016).
Ubiquitylation of 26S proteasomes has been shown to have multiple effects. Extensive ubiquitylation of the yeast and
Arabidopsis
particles directs non-functional complexes for autophagic degradation
via specific receptors that bind to both the ubiquitin moieties on the
impacted proteasome subunits and ATG8 (
Marshall et al., 2015,
2016;
Cohen-Kaplan et al., 2016;
see below). As mentioned above, specific ubiquitylation of the
proteasomal ubiquitin receptors Rpn10 and Rpn13 suppresses their ability
to recognize substrates (
Isasa et al., 2010;
Lipinszki et al., 2012;
Jacobson et al., 2014;
Zuin et al., 2015), while ubiquitylation of Rpt5 appears to be an important checkpoint during Rpt ring assembly (
Fu et al., 2018).
The function(s) of other 26S proteasome modifications are
less well-defined. The Rpt2 subunit of the RP has been shown to be
N-myristoylated in multiple species, which could tether proteasomes to
membrane surfaces (
Shibahara et al., 2002;
Gomes et al., 2006;
Kimura et al., 2012,
2016).
In yeast, the N-terminus of Rpt1 is mono- or di-methylated, and a
mutant strain blocking this modification is more sensitive to
proteotoxic stress induced by hydrogen peroxide or the amino acid analog
canavanine (
Kimura et al., 2013). Other examples include glutathionylation of the α
5 subunit, which might affect gating of the yeast CP (
Demasi et al., 2003;
Silva et al., 2012),
and attachment of N-acetylgalactosamine to mammalian RPT2, which
inhibits the ATPase ring of the RP base and hence reduces overall
proteasome degradation rates (
Zhang et al., 2003).
A role for N-acetylation of proteasome subunits by the NatB complex in
assembling PSGs has been inferred from the effects of Δ
nat3 and Δ
mdm20 mutants on this re-localization (
van Deventer et al., 2015;
Marshall and Vierstra, 2018b). Further work is clearly needed to establish the reasons for the myriad of other modifications.
Autophagy-Mediated Control of 26S Proteasome Abundance
While the synthesis and assembly of proteasomes has been
studied for over a decade, their turnover had remained obscure until
recently. Proteasomes are stable complexes (
Pack et al., 2014), with a half-life of 16 h in mouse embryonic fibroblasts (
Tomita et al., 2019) and over 2 weeks when measured in rat liver cells (
Tanaka and Ichihara, 1989),
but under specific conditions their degradation can be rapid and
extensive. One turnover mechanism involves caspase-mediated cleavage.
Following induction of apoptosis in human cells, the RP subunits RPT5,
RPN2 and RPN10 are cleaved by caspase-3, resulting in impaired
proteasome activity and the accumulation of ubiquitylated substrates (
Sun et al., 2004). Similarly, caspase-3 activation in
D. melanogaster cells leads to cleavage of the α
2, α
4 and β
4 subunits of the CP, and the RPT1 subunit of the RP (
Adrain et al., 2004).
Presumably these impaired proteasomes are then removed, possibly by
autophagy (see below). A second pathway is the removal of non-functional
proteasome subunits by the UPS itself prior to their integration into
the holo-proteasome. Hsp42 was shown to be important in yeast by
coalescing these polypeptides into cytoplasmic condensates from which
they are cleared by active 26S proteasomes (
Peters et al., 2015;
Nahar et al., 2019).
A third pathway for degrading 26S proteasomes that has
recently gained in appreciation is autophagy, via a route termed
proteaphagy (
Figure 5;
Marshall and Vierstra, 2015;
Marshall et al., 2015,
2016).
Autophagy involves the delivery of cytoplasmic material to the vacuole
(in plants and yeast) or lysosome (in mammals) for breakdown by resident
hydrolases (
Reggiori and Klionsky, 2013;
Gatica et al., 2018;
Marshall and Vierstra, 2018a;
Levine and Kroemer, 2019).
It is the preferred catabolic route for large, heterogeneous
cytoplasmic material, such as protein aggregates, organelles, lipid
droplets, or even invading pathogens whose sizes exceed the spatial
capacity of proteasomes. The defining feature of the most common
autophagic route, macroautophagy (referred to here as autophagy), is the
de novo formation of a cup-shaped membrane called the phagophore
(or isolation membrane) that encircles portions of cytoplasm. The
phagophore ultimately seals to generate a double membrane-bound
autophagosome, the outer membrane of which then fuses with the vacuole
or lysosome to release the internal vesicle as an autophagic body (see
Figure 6).
The contents of the autophagic body and its limiting membrane are
rapidly consumed by a collection of vacuolar hydrolases with acidic pH
optima (
Parzych and Klionsky, 2018),
with the constituent amino acids, fatty acids, carbohydrates and
nucleotides ultimately re-used for survival or to power new growth.
Figure 5. Pathways for Autophagic Degradation of 26S Proteasomes. (A)
A model for starvation-induced proteasome degradation versus storage in
yeast. When cells are subjected to nitrogen or carbon starvation, 26S
proteasomes dissociate into the CP and RP sub-complexes and are exported
from the nucleus via the exportin Crm1. Upon nitrogen starvation, the
CP and RP coalesce into cytoplasmic foci in a Snx4/41/42-dependent
manner. They are then encapsulated by the expanding phagophore and
delivered to the vacuole for degradation, a process requiring the Atg1
kinase complex and the Atg8 lipidation machinery. Deubiquitylation of
one or more CP subunits by Ubp3/Bre5 may also be required. Whether
specific Atg8-binding autophagy receptors are involved remains unknown.
In contrast, carbon starvation, which results in cytoplasmic
acidification and reduced ATP levels, triggers re-localization of the CP
and RP into cytoplasmic proteasome storage granules (PSGs). This
accretion requires numerous factors, including Blm10 for the CP, Spg5
and the C-terminus of Rpn11 for the RP, and the NatB N-terminal
acetylation complex (consisting of Nat3 and Mdm20) for both. PSGs act to
store proteasome sub-complexes and protect them from autophagic
degradation. Preventing sequestration of proteasomes into PSGs leads to
their Atg1- and Atg8-dependent turnover. (B) A model
for starvation-induced proteasome degradation in humans. When HeLa cells
are subjected to amino acid starvation, the proteasome subunits RPN1,
RPN10, and RPN13 become poly-ubiquitylated by one or more E3 ligases,
facilitating their recognition by the autophagy receptor p62/SQSTM1. By
simultaneous interaction with lipidated ATG8/LC3, p62 delivers inactive
proteasomes to the expanding phagophore for eventual turnover by
autophagy, a process requiring the TOR kinase and the ATG8/LC3
lipidation machinery. (C) A model for inhibitor-induced proteaphagy in Arabidopsis
and yeast. Proteasomes subjected to chemical or genetic inhibition,
including by the pathogen effector HopM1, are exported from the nucleus
and aggregate in an Hsp42-dependent manner into insoluble protein
deposit (IPOD)-like structures that are distinct from PSGs. The
aggregated proteasomes are then ubiquitylated by one or more E3 ligases,
facilitating their recognition by the selective proteaphagy receptors
Cue5 in yeast or RPN10 in Arabidopsis. By simultaneous
interactions with lipidated ATG8, these receptors deliver inactive
proteasomes to enveloping autophagic vesicles for final turnover in the
vacuole. PE, phosphatidylethanolamine; PI3P,
phosphatidylinositol-3-phosphate.
Figure 6. The Life Cycle of a 26S Proteasome.
Proteasome subunit synthesis from individual amino acids is regulated by
transcription factors such as Rpn4 in yeast, NRF1 in mammals, and
NAC53/NAC78 in plants, the activities of which are sensitive to changing
physiological conditions, in particular proteotoxic stress. The various
subunits then assemble in a co-ordinated manner to form the mature
holo-26S proteasome, with assistance from a suite of dedicated
chaperones. Proteasomes localize to either the cytosol or nucleus, where
their activity can be regulated by an array of post-translational
modifications and associated factors. They ultimately recognize and
degrade poly-ubiquitylated substrates in a process mediated by intrinsic
and extrinsic ubiquitin receptors. Finally, excess or damaged
proteasomes can be degraded in the vacuole or lysosome via one of
several autophagic pathways, some which are mediated by signals from the
nutrient-responsive Atg1 kinase, subunit ubiquitylation, and/or a
variety of autophagy receptors, including Cue5 in yeast, p62/SQSTM1 in
mammals, and RPN10 in plants. Autophagic degradation of 26S proteasomes
recycles amino acids, which can then be used for the synthesis of new
particles.
Through studies on a variety of
organisms over the past two decades,
the core machinery underpinning
autophagy has emerged, driven by a conserved collection of
“autophagy-related” (Atg) proteins. These are traditionally classified
into distinct biochemical and functional groups that act at specific
stages during autophagy, and include:
(i) the Atg1 serine/threonine
kinase complex that initiates autophagy in response to upstream signals
from nutrient-sensitive kinases, such as Snf1 and Tor1/2;
(ii) the Atg9
transmembrane protein required for membrane delivery;
(iii) the class
III phosphatidylinositol-3-kinase (PI3K) complex that generates the
phosphatidylinositol-3-phosphate (PI3P) signal important for
autophagosome nucleation;
(iv) the Atg2-Atg18 complex involved in
membrane extension at the site of PI3P labeling; and
(v) the
ubiquitin-fold protein Atg8 and its conjugation machinery that are
crucial for autophagosome dynamics and cargo recruitment (
Ohsumi, 2001;
Marshall and Vierstra, 2018a;
Levine and Kroemer, 2019).
Atg8 (known as MAP1LC3 or GABARAP in mammals) is the
signature element of the autophagy system. Its functions depend on
attachment to the lipid phosphatidylethanolamine (PE) via a conjugation
cascade mechanistically analogous to ubiquitylation. Atg8 is activated
by the E1 Atg7, transferred to the E2 Atg3, and finally connected via an
ether linkage to PE by a hexameric E3 ligase complex comprised of a
conjugate between Atg5 and Atg12 which is then bound to Atg16.
Lipidated Atg8 becomes embedded in the autophagic
membranes, where it serves two purposes. One is to promote membrane
expansion, autophagosome closure, and final docking with the vacuole or
lysosome through interactions with a collection of adaptors that bind
both components of the vesicular transport machinery and the Atg8-PE
adduct. The other is to tether cargo to the enveloping phagophore
through interactions between Atg8-PE and a plethora of receptors that
recognize specific cargo (
Rogov et al., 2014;
Farré and Subramani, 2016;
Gatica et al., 2018;
Marshall and Vierstra, 2018a).
The best-known adaptors/receptors bind Atg8 with low micromolar
affinity through an Atg8-interacting motif [AIM, also called an
LC3-interacting region (LIR)] bearing two hydrophobic residues that
insert into complementary hydrophobic pockets on the surface of Atg8 (
Noda et al., 2008,
2010;
Klionsky and Schulman, 2014;
Maqbool et al., 2016;
Rogov et al., 2018), although additional binding mechanisms have recently been described (
Marshall et al., 2019).
Through a rapidly expanding collection of receptors, a
wide array of selective autophagic routes have emerged, including
dedicated pathways for clearing protein aggregates, stress granules,
mitochondria, peroxisomes, chloroplasts, ER, nuclear components, lipid
bodies, ribosomes, and intracellular pathogens (
Kraft et al., 2008;
Mochida et al., 2015;
Farré and Subramani, 2016;
Khaminets et al., 2016;
Yamano et al., 2016;
Gatica et al., 2018;
Marshall and Vierstra, 2018a;
Wyant et al., 2018). As will be described below, proteasomes are also rapidly cleared by autophagy using at least two proteaphagic routes (
Marshall and Vierstra, 2015;
Marshall et al., 2015,
2016;
Cohen-Kaplan et al., 2016;
Waite et al., 2016;
Nemec et al., 2017).
Autophagic Degradation of 26S Proteasomes Upon Nutrient Starvation
Autophagic flux is up-regulated upon nutrient
starvation, which includes lack of nitrogen, fixed-carbon, phosphate,
and various micronutrients such as zinc, resulting in the bulk
degradation of cytoplasmic material, often in a non-specific manner (
Takeshige et al., 1992;
Thompson et al., 2005;
Adachi et al., 2017;
Kawamata et al., 2017).
Early hints that 26S proteasomes could be targets for autophagic
degradation came from immuno-electron microscopy studies that observed
20S proteasome subunits in rat liver lysosomes, particularly upon
starvation (
Cuervo et al., 1995). Subsequently, multiple proteomic studies cataloging autophagosome contents identified proteasome subunits as cargo (
Gao et al., 2010;
Dengjel et al., 2012;
Mancias et al., 2014;
Le Guerroué et al., 2017),
while more recent multi-omics studies in humans and maize confirmed
that proteasomes are extensively degraded by both basal and
starvation-induced autophagy (
Zhang et al., 2016;
McLoughlin et al., 2018).
Autophagic degradation of proteasomes can easily be
visualized using subunits tagged with GFP or other fluorescent
reporters. For example, transfer of the fluorescent signals from the
nucleus and cytoplasm to autophagic bodies in the vacuole is evident
within hours of nitrogen starvation in both
Arabidopsis and yeast, and within 12 h almost all proteasomes from both organisms have moved to the vacuole via autophagy (
Figures 4C,E).
This transfer and subsequent breakdown can then be quantified by
immunoblot analysis of the proteasome subunits fused to GFP-type
reporters (
Figure 4F).
Whereas, the tagged proteasome subunit is rapidly degraded as the
autophagic body breaks down, the GFP moiety is remarkably stable and
accumulates in the vacuole. The ratio of the GFP fusion to free GFP thus
provides a reliable assay to measure autophagic turnover rates. Using
this assay in yeast, it was shown that more than 80% of cellular
proteasomes are degraded by autophagy after 8 h of nitrogen starvation (
Figure 4F;
Marshall et al., 2016).
The starvation-induced autophagic degradation of proteasomes, along with similarly abundant ribosomes (
Kraft et al., 2008;
Wyant et al., 2018),
will rapidly provide a pool of free amino acids that can sustain cell
viability when nitrogen is scarce. Given the fast induction of autophagy
when nutrients are limiting (
Takeshige et al., 1992;
Thompson et al., 2005),
proteasomes themselves probably play little role in starvation-induced
degradation of cellular proteins. The fact that proteasomes are
restricted to degrading proteins one at a time, coupled with the high
energy requirements of the ubiquitylation machinery and the proteasome
itself (
Peth et al., 2013b;
Collins and Goldberg, 2017),
likely make bulk autophagic degradation of whole proteasomes and other
cellular material a more effective strategy for rapid nutrient
re-mobilization than up-regulation of the UPS.
A significant barrier to the recruitment of proteasomes
to phagophores is the fact that most proteasomes are located in the
nucleus (
Reits et al., 1997;
Enenkel et al., 1998;
Russell et al., 1999;
Brooks et al., 2000;
Pack et al., 2014;
Marshall et al., 2015),
whereas the autophagy machinery is found exclusively in the cytosol.
Little is currently known about autophagic degradation of nuclear
components. In mammals, autophagy of nuclear lamina has been reported (
Dou et al., 2015),
while in budding yeast, a pathway called piecemeal microautophagy of
the nucleus (PMN) has been described that requires nuclear-vacuole
junctions formed by Nvj1, Lam5 and Lam6 (
Roberts et al., 2003;
Krick et al., 2008;
Mijaljica et al., 2012;
Elbaz-Alon et al., 2015). More recently, selective autophagy of nuclear components mediated by the receptor Atg39 was also reported (
Mochida et al., 2015), a process distinct from PMN.
Initial studies on the degradation of nuclear
proteasomes following nitrogen starvation in yeast surprisingly revealed
that neither Atg39-mediated nucleophagy nor components of the PMN
pathway were required (
Marshall et al., 2016;
Waite et al., 2016;
Nemec et al., 2017). Instead, a role for direct nuclear export of proteasomes mediated by the exportin Crm1 appears crucial (
Stade et al., 1997;
Hutten and Kehlenbach, 2007). Notably, a temperature-sensitive
CRM1 allele (termed
xpo1-1)
that strongly interferes with Crm1-dependent nuclear export
substantially attenuates proteaphagy at non-permissive temperatures,
although bulk autophagic flux remains unaffected (
Figure 5A;
Nemec et al., 2017).
In addition to Crm1, targeted deletion of a suite of
autophagy components revealed many factors required for
starvation-induced proteaphagy in yeast (
Figure 5A).
These include all subunits of the Atg1 and PI3K complexes, the entire
Atg8 lipidation pathway, the Atg9 membrane delivery system, the vacuolar
protease Pep4, the vacuolar phospholipase Atg15 that degrades the
autophagic body membrane, and the sorting nexins Snx4/Atg24 and Snx41 or
Snx42 (which function as Snx4-Snx41 or Snx4-Snx42 heterodimers, with
Snx41 and Snx42 acting redundantly;
Marshall et al., 2016;
Waite et al., 2016;
Nemec et al., 2017).
Presumably, the involvement of Atg1 allows starvation signals emanating
from up-stream nutrient-responsive kinases, such as Snf1 and Tor1/2 to
up-regulate 26S proteasome clearance. The involvement of the sorting
nexins suggests that starvation-induced proteaphagy is selective, as
Snx4, Snx41 and/or Snx42 are not required for bulk autophagy in yeast (
Nice et al., 2002;
Reggiori and Klionsky, 2013). This mirrors the situation for ribosomes, which are selectively targeted for degradation in response to starvation (
Kraft et al., 2008;
Wyant et al., 2018). Snx4 is also required for autophagic clearance of the fatty acid synthase complex (
Shpilka et al., 2015) and the small and large subunits of the ribosome (
Nemec et al., 2017),
suggesting that it might assist in degrading large protein complexes
more generally. Interestingly, the sorting nexins appear to promote the
formation of proteasome-containing cytoplasmic puncta that accumulate
when autophagy is impaired (
Waite et al., 2016;
Nemec et al., 2017).
Multiple lines of evidence suggest that the CP and RP
likely dissociate in the nucleus prior to their autophagic degradation.
For example, turnover of the CP, but not the RP, upon nitrogen
starvation in yeast was shown to be dependent upon the DUB Ubp3,
suggesting that the two sub-complexes are degraded by separate routes (
Waite et al., 2016;
Marshall and Vierstra, 2018b). Using the “anchor-away” technique to tether the CP or RP sub-complexes in either the cytoplasm or nucleus (
Haruki et al., 2008),
Nemec et al. (2017)
showed that disassembly of the CP, RP lid and RP base occurs prior to
nuclear export, as CP or RP base degradation was not impacted when the
RP lid was anchored inside the nucleus. It is currently unclear why
CP-RP dissociation is necessary for proteaphagy, as fully assembled
proteasomes have been reported to pass intact through the nuclear pore
on their way into the nucleus (
Savulescu et al., 2011;
Pack et al., 2014). However, because CP activity is much lower when separated from the RP (
Groll et al., 2000;
Dambacher et al., 2016),
dissociation of the nuclear 26S particles into sub-complexes might help
attenuate CP activity until encapsulated by autophagosomes, thus
preventing a sudden influx of active 26S proteasomes into the cytosol
that could interfere with proteostasis in this compartment.
While proteasomes are rapidly degraded by autophagy upon
nitrogen starvation, they surprisingly remain stable upon carbon
starvation in both plants and yeast (
Figure 5A;
Waite et al., 2016;
Marshall and Vierstra, 2018b), even though this treatment also activates bulk autophagy (
Takeshige et al., 1992;
Thompson et al., 2005;
Adachi et al., 2017).
Instead, carbon starvation leads to dissociation of the CP and RP,
followed by their rapid export out of the nucleus and subsequent
re-location into discrete PSGs that appear within an hour of transfer to
carbon-free media (
Figures 4B–D,
5A;
Laporte et al., 2008;
Marshall and Vierstra, 2018b).
Surprisingly, 26S proteasome levels also remain stable upon
simultaneous nitrogen and carbon starvation, implying that carbon
starvation overrides the proteaphagic response elicited by the lack of
nitrogen.
Cytologically, PSGs appear as membrane-less condensates
that coalesce in response to the reduced ATP levels and/or cytoplasmic
acidification that occur in the absence of a carbon source (
Laporte et al., 2008;
Peters et al., 2013;
Sagot and Laporte, 2019).
These puncta seemingly dissolve within minutes when carbon availability
improves, suggesting that they represent a storage form of the complex.
More than 40 factors have been identified that affect PSG formation (
Gu et al., 2017),
including Blm10 (for the CP), Spg5 and the C terminus of Rpn11 (for the
RP), and the NatB N-terminal acetylation complex for both (
Hanna et al., 2012;
Saunier et al., 2013;
Weberruss et al., 2013;
van Deventer et al., 2015;
Marshall and Vierstra, 2018b),
but it remains unclear how many of these factors participate directly
in PSG formation. By analogy with other liquid-liquid phase separation
events (
Alberti et al., 2019;
Wang and Zhang, 2019), unstructured regions within proteasome subunits could contribute to this condensation (
Aufderheide et al., 2015b).
The reasons for proteasome accretion into PSGs were
initially enigmatic. However, observations that PSGs also form as yeast
enter quiescence (
Laporte et al., 2008), and that the sequestration of proteasomes into PSGs is antagonistic to proteaphagy (
Marshall and Vierstra, 2018b),
implied that PSGs act to store proteasomes under conditions that
reduced growth due to lack of energy. In particular, attenuation of PSG
assembly upon carbon starvation through mutants eliminating Blm10, Spg5,
and NatB, or truncating Rpn11, strongly re-directs 26S proteasomes to
autophagy, suggesting that proteaphagy is the default response to
starvation, with PSGs providing a novel adaptation to save proteasomes
during carbon stress (
Marshall and Vierstra, 2018b).
The ability to store proteasomes in turn confers
increased cell fitness to yeast. PSG formation during stationary phase,
upon replicative aging, or in response to carbon starvation promotes
rapid resumption of cell growth when nutrient availability improves (
van Deventer et al., 2015;
Marshall and Vierstra, 2018b), while blocking PSG formation instead suppresses the ability of cells to resume growth upon restoration of a carbon source (
Marshall and Vierstra, 2018b).
Presumably, the retained proteasomes enable more rapid initiation of
cell division, given the importance of 26S proteasomes, and the UPS in
general, for degrading regulators responsible for cell cycle progression
(
Ciechanover et al., 1984;
Goebl et al., 1988).
Autophagic degradation of proteasomes in response to amino acid starvation has also been reported in mammals (
Figure 5B;
Cohen-Kaplan et al., 2016). Surprisingly, and in contrast to the situation in plants and yeast (
Marshall et al., 2015,
2016), starvation-induced proteaphagy in HeLa cells is accompanied by increased subunit ubiquitylation on RPN1, RPN10 and RPN13 (
Cohen-Kaplan et al., 2016).
The attached poly-ubiquitin chains appear essential for proteaphagy, as
siRNA-mediated silencing of the E1 or over-expression of a ubiquitin
variant lacking the internal lysine residues necessary for chain
concatenation reduced rates of proteasome degradation. This turnover
requires the autophagy receptor p62/SQSTM1, which recognizes
ubiquitylated cargo via its UBA domain and ATG8/LC3 via a canonical AIM (
Noda et al., 2008,
2010;
Cohen-Kaplan et al., 2016).
It thus appears that, at least in the HeLa cell system, starvation
induces significant ubiquitylation of proteasomes to promote recognition
by the autophagy machinery (
Figure 5B;
Cohen-Kaplan et al., 2016).
More recently, the Atg16 homolog ATG16L1 was implicated in proteaphagy in the social amoeba
Dictyostelium discoideum (
Xiong et al., 2018). Unexpectedly, ATG16L1 directly binds to RPN1 and RPN2
in vitro, and co-localizes with these subunits in autophagosome-type puncta decorated with ATG8
in vivo. As
D. discoideum
undergoes a dramatic transformation from a single amoeba into a social
pseudopod upon nutrient starvation, an appealing notion is that the
interaction of ATG16L1 with 26S proteasomes provides a direct way to
tether the particles to the enveloping autophagic membranes during
starvation-induced proteaphagy (
Xiong et al., 2018).
Taken together, while starvation-induced proteaphagy is likely
universal, the mechanism(s) and identity of the receptor(s) involved (if
any) likely vary among eukaryotes (
Marshall et al., 2015,
2016;
Cohen-Kaplan et al., 2016;
Xiong et al., 2018).
Autophagic Degradation of Inactive 26S Proteasomes
In addition to starvation-induced proteaphagy, a second
pathway has been described in plants and yeast that enables clearance of
non-functional 26S proteasomes (
Marshall et al., 2015,
2016;
Nemec et al., 2017). This proteaphagic route occurs independently of the Atg1 kinase, and can be stimulated
in vivo
by treatment with chemical inhibitors, such as MG132 and bortezomib, by
genetic mutations that impair CP or RP assembly, and even by pathogen
effectors, such as HopM1 from
Pseudomonas syringae (
Figure 5C;
Marshall et al., 2015,
2016;
Üstün et al., 2018). In both
Arabidopsis and yeast, proteasome inhibition leads to the accumulation of ubiquitylated species associated with the complex (
Marshall et al., 2015,
2016).
These species are not stalled targets awaiting turnover, but instead
reflect extensive modification of the 26S proteasome itself (
Book et al., 2010;
Kim et al., 2013;
Marshall et al., 2015,
2016).
The identities of the modified subunits are not yet known, but analysis
of the CP and RP sub-complexes individually suggests that RP subunits
are dominant targets (R. S. Marshall and R. D. Vierstra, unpublished
data). Subsequent studies revealed that these ubiquitin moieties are
recognized by selective autophagy receptors, which then bridge the
inhibited, ubiquitylated proteasomes to Atg8 lining the expanding
phagophore (
Figure 5C).
The autophagy receptor for clearing inhibited proteasomes in
Arabidopsis
is RPN10, which uses two distinct UIMs to tether proteasomes to the
enveloping autophagic vesicle. One UIM binds the ubiquitin moieties
attached to 26S proteasomes, while the other surprisingly binds ATG8 (
Marshall et al., 2015,
2019).
This non-canonical, UIM-mediated interaction between RPN10 and ATG8 is
striking, as it does not involve the canonical LIR/AIM docking site
(LDS) on ATG8, but instead requires an alternative hydrophobic patch
recently termed the UIM docking site (UDS;
Marshall et al., 2019). The yeast version of Rpn10 is truncated compared to its
Arabidopsis
counterpart, meaning it lacks the Atg8-binding UIM sequence and
consequently has no discernable role in proteaphagy. Instead, Cue5 acts
as the yeast receptor for ubiquitylated proteasomes, using a CUE domain
to bind ubiquitin and a canonical AIM to bind Atg8 (
Figure 5C;
Marshall et al., 2016). The UIM1-UIM2 pairing for
Arabidopsis
RPN10 and the CUE-AIM pairing for Cue5 thus provides an elegant example
of convergent evolution, where different interacting motifs are
exploited to generate the same outcome, namely tethering of
ubiquitylated proteasomes to autophagic membranes.
Cue5 and its human counterpart TOLLIP have been implicated in the autophagic clearance of various aggregation-prone proteins (
Lu et al., 2014)
and, intriguingly, inhibitor-induced proteaphagy in yeast is likewise
preceded by aggregation of 26S proteasomes into peri-vacuolar insoluble
protein deposit (IPOD)-type structures (
Kaganovich et al., 2008;
Marshall et al., 2016),
suggesting some degree of overlap between the proteaphagy and
aggrephagy machineries. The IPODs seen upon proteasome inhibition are
distinct from PSGs (
Marshall and Vierstra, 2018b), although there might be some overlap between the two types of puncta during early stages of carbon starvation (
Peters et al., 2016).
The two condensates can be easily distinguished based on their
co-localization with either Blm10 (in PSGs) or the aggregation-prone
prion protein Rnq1 (in IPODs;
Figure 4B).
IPOD formation is dependent on the oligomeric chaperone Hsp42, which helps coalesce aggregated proteins (
Specht et al., 2011;
Malinovska et al., 2012;
Miller et al., 2015).
The accumulation of yeast 26S proteasomes into IPODs upon inhibition,
and their subsequent autophagic breakdown, were also found to require
this aggregase (
Marshall et al., 2016).
Where inactive 26S proteasomes become ubiquitylated is currently
unclear; one possibility is that dysfunctional proteasomes are first
ubiquitylated and then delivered to IPODs with the help of Hsp42, while
the other is that Hsp42 first delivers dysfunctional proteasomes into
IPODs, which are then ubiquitylated through one or more IPOD-resident
E3s.
Whereas chemical inhibitors compromising the CP induce
autophagic degradation of both CP and RP, possibly due to the tighter
interaction between the two sub-complexes that allosterically results
from CP inhibition (
Kleijnen et al., 2007),
mutations that compromise proteasome assembly instead appear to induce
turnover of the affected CP and RP sub-particles separately. For
example, the
doa5-1 allele that compromises the α
5 subunit of the CP triggers the Cue5-dependent turnover of the rest of the CP, but not the RP, while the
rpn5Δ
C mutation impacting Rpn5 triggers the Cue5-dependent turnover of the rest of the RP, but not the CP (
Marshall et al., 2016).
These observations imply that proteaphagy can be initiated for both the
whole 26S particle, and for the individual CP and RP sub-complexes
separately.
Clearly, an important feature of inhibitor-induced
proteaphagy is its ability to discriminate between functional and
dysfunctional particles. One possibility is that stalled or compromised
26S proteasomes acquire a distinct conformation that is recognized by
Hsp42 and/or the ubiquitylation machinery, which directs their
accumulation into IPODs. An intriguing factor in this scenario was
Ecm29, as it binds specifically to mutant forms of 26S proteasomes, and
thus could detect inappropriate conformations induced by inactivation (
Lehmann et al., 2010;
Lee S. Y. et al., 2011;
Panasenko and Collart, 2011;
Park et al., 2011). However, analysis of yeast Δ
ecm29 mutants suggested this it is not involved in proteaphagy (
Marshall and Vierstra, 2018b). Several E3s have been detected in association with 26S proteasomes that could instead provide this quality control (
Xie and Varshavsky, 2000;
Crosas et al., 2006;
Panasenko and Collart, 2011), some of which ubiquitylate specific subunits (
Besche et al., 2014;
Fu et al., 2018),
but their function(s) in relation to proteaphagy, if any, remain to be
determined. Further work is certainly required to fully unravel the
mysteries surrounding this last chapter in the life of a proteasome.
Conclusions and Perspectives
Since the discovery of the UPS over three decades ago,
great progress has been made in our understanding of selective
proteolysis by this system. This includes intricate knowledge of the 26S
proteasome itself, which combines strict substrate selectivity with
extreme promiscuity with respect to substrate processing to enable the
degradation of thousands of proteins with exquisite specificity. Recent
technological advances in cryo-EM imaging have generated increasingly
detailed models describing substrate recognition and processing by the
26S proteasome (
Lander et al., 2012;
Lasker et al., 2012;
Bhattacharyya et al., 2014;
de la Peña et al., 2018;
Dong et al., 2019;
Finley and Prado, 2019).
In parallel, a multitude of additional studies across several kingdoms
have advanced our knowledge of the 26S proteasome life cycle, including
its biosynthesis, assembly, localization, and ultimately turnover (
Figure 6;
Collins and Goldberg, 2017;
Rousseau and Bertolotti, 2018).
The combined studies reveal the use of common mechanisms to control 26S
proteasome assembly, activity, and degradation, though often by
exploiting distinct factors and machineries.
However, despite these advances, much remains unknown.
Areas of continued uncertainty include, but are not limited to: (i)
which transcription factors are responsible for proteasome gene
expression under non-stressed conditions in plants and yeast; (ii) the
identities of additional proteasome assembly chaperones, particularly
for the RP lid; (iii) how ubiquitin-chain topologies and the geometric
or structural features of the substrate influence recognition and
turnover by the proteasome; (iv) how extrinsic factors,
proteasome-interacting proteins, and post-translational modifications
regulate the various proteasome activities; (v) whether proteasomes are
selectively chosen for proteaphagy during nutrient starvation using
dedicated receptor(s), or degraded in bulk along with the rest of the
cytoplasm; and (vi) how dysfunctional proteasomes are detected prior to
autophagic degradation, and which subunit(s) are ubiquitylated by which
E3(s).
The UPS is involved in nearly all cellular processes in
eukaryotes, and its mis-regulation often contributes to aging and
disease, or loss of crop yield (
Saez and Vilchez, 2014;
Rape, 2018;
Li et al., 2019).
This has fed a desire to understand the dynamic regulation of
proteasomes, simultaneously advancing our knowledge of basic cellular
processes that control this proteolytic machine, and providing a
potential avenue for the development of novel therapies to ameliorate a
variety of diseases related to 26S proteasomes and their activity.
Author Contributions
RSM and RDV conceived the article, prepared the figures,
and wrote the manuscript. Both authors have made a substantial, direct
and intellectual contribution to the work, and approved it for
publication.
Funding
This work was supported by grants from the National
Institutes of Health, National Institute of General Medical Science
(R01-GM124452) and the National Science Foundation, Plant Genome
Research Program (IOS-1339325).
Conflict of Interest Statement
The authors declare that the research was conducted in
the absence of any commercial or financial relationships that could be
construed as a potential conflict of interest.
Acknowledgments
The authors thank past and present members of the
Vierstra lab for many stimulating discussions on the topics covered in
this manuscript.
Richard S. Marshall* and 
Richard D. Vierstra*