KLHL13(Xq24), BKLHD2. Tarkka kromosomisegrekaatio ja sytokineesi
https://www.ncbi.nlm.nih.gov/gene/90293
- Also known as
- BKLHD2
- Summary
- This gene encodes a BTB and kelch domain containing protein
and belongs to the kelch repeat domain containing superfamily of
proteins. The encoded protein functions as an adaptor protein that
complexes with Cullin 3 and other proteins to form the Cullin 3-based E3
ubiquitin-protein ligase complex. This complex is necessary for proper
chromosome segregation and completion of cytokinesis. Alternate splicing
results in multiple transcript variants. [provided by RefSeq, Mar 2010]
- Expression Broad expression in endometrium (RPKM 9.9), kidney (RPKM 3.7) and 15 other tissues See more
- Preferred Names
- kelch-like protein 13
- Names
- BTB and kelch domain containing 2
- kelch-like 13
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A Cul3-based E3 ligase regulates mitosis and is required to maintain the spindle assembly checkpoint in human cells.
Sumara I, et al. Cell Cycle, 2007 Dec 15. PMID 18075312. The spindle assembly checkpoint (SAC) is a mechanism that prevents
premature chromosome segregation in anaphase before all chromosomes are
correctly attached to the mitotic spindle. Errors in chromosome
segregation lead to aneuploidy, which may be causally involved in
tumorgenesis. Kinetochore complexes are the structural components of the
SAC, which are tightly regulated by various mechanisms including
phosphorylation and ubiquitin-dependent proteolysis. Recent studies shed
new light on the regulatory pathways of the ubiquitin proteasome system
involved in SAC signaling. Here we present evidence that a Cul3-based
E3 ubiquitin-ligase is required to maintain SAC signaling in human
cells. Inactivation of the Cul3/KLHL9/KLHL13
ligase leads to premature degradation of Cyclin B and exit from the
mitotic state in the presence of microtubule poisons. We discuss
possible mechanisms how Cul3 may be required to maintain SAC activity by
ubiquitination of the chromosomal passenger protein Aurora B.
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A
Cul3-based E3 ligase removes Aurora B from mitotic chromosomes,
regulating mitotic progression and completion of cytokinesis in human
cells.
Sumara I, et al. Dev Cell, 2007 Jun. PMID 17543862. Faithful cell-cycle progression is tightly controlled by the
ubiquitin-proteasome system. Here we identify a human Cullin 3-based E3
ligase (Cul3) which is essential for mitotic division. In a complex with
the substrate-specific adaptors KLHL9 and KLHL13, Cul3 is required for
correct chromosome alignment in metaphase, proper midzone and midbody
formation, and completion of cytokinesis. This Cul3-based E3 ligase
removes components of the chromosomal passenger complex from mitotic
chromosomes and allows their accumulation on the central spindle during
anaphase. Aurora B directly binds to the substrate-recognition domain of
KLHL9 and KLHL13 in vitro, and coimmunoprecipitates with the Cul3
complex during mitosis. Moreover, Aurora B is ubiquitylated in a
Cul3-dependent manner in vivo, and by reconstituted Cul3/KLHL9/KLHL13
ligase in vitro. We thus propose that the Cul3/KLHL9/KLHL13 E3 ligase
controls the dynamic behavior of Aurora B on mitotic chromosomes, and
thereby coordinates faithful mitotic progression and completion of
cytokinesis.
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USP25 regulates Wnt signaling by controlling the stability of tankyrases.
Xu D, et al. Genes Dev, 2017 May 15. PMID 28619731, Free PMC Article
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The Cul3-KLHL21 E3 ubiquitin ligase targets aurora B to midzone microtubules in anaphase and is required for cytokinesis.
Maerki S, et al. J Cell Biol, 2009 Dec 14. PMID 19995937, Free PMC ArticleCul3 (Cullin3)-based E3 ubiquitin ligases recently emerged as critical
regulators of mitosis. In this study, we identify two mammalian BTB
(Bric-a-brac-Tramtrack-Broad complex)-Kelch proteins, KLHL21 and KLHL22,
that interact with Cul3 and are required for efficient chromosome
alignment. Interestingly, KLHL21 but not KLHL22 is necessary for
cytokinesis and regulates translocation of the chromosomal passenger
complex (CPC) from chromosomes to the spindle midzone in anaphase,
similar to the previously described BTB-Kelch proteins KLHL9 and KLHL13.
KLHL21 directly binds to aurora B and mediates ubiquitination of aurora
B in vitro. In contrast to KLHL9 and KLHL13, KLHL21 localizes to
midzone microtubules in anaphase and recruits aurora B and Cul3 to this
region. Together, our results suggest that different Cul3 adaptors
nonredundantly regulate aurora B during mitosis, possibly by
ubiquitinating different pools of aurora B at distinct subcellular
localizations.
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Dimerization quality control ensures neuronal development and survival.
Mena EL, et al. Science, 2018 Oct 12. PMID 30190310
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