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本文引用的文献

1
Unique and redundant β-catenin regulatory roles of two Dishevelled paralogs during C. elegans asymmetric cell division.秀丽隐杆线虫不对称细胞分裂过程中两个Dishevelled旁系同源物独特且冗余的β-连环蛋白调节作用。
J Cell Sci. 2016 Mar 1;129(5):983-93. doi: 10.1242/jcs.175802. Epub 2016 Jan 21.
2
Quantitative Differences in Nuclear β-catenin and TCF Pattern Embryonic Cells in C. elegans.秀丽隐杆线虫中核β-连环蛋白和TCF模式胚胎细胞的定量差异
PLoS Genet. 2015 Oct 21;11(10):e1005585. doi: 10.1371/journal.pgen.1005585. eCollection 2015 Oct.
3
Asymmetric Wnt Pathway Signaling Facilitates Stem Cell-Like Divisions via the Nonreceptor Tyrosine Kinase FRK-1 in Caenorhabditis elegans.不对称Wnt信号通路通过秀丽隐杆线虫中的非受体酪氨酸激酶FRK-1促进类干细胞分裂。
Genetics. 2015 Nov;201(3):1047-60. doi: 10.1534/genetics.115.181412. Epub 2015 Sep 9.
4
Centrosome-intrinsic mechanisms modulate centrosome integrity during fever.中心体内在机制在发热期间调节中心体完整性。
Mol Biol Cell. 2015 Oct 1;26(19):3451-63. doi: 10.1091/mbc.E15-03-0158. Epub 2015 Aug 12.
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Dynamic localization of Mps1 kinase to kinetochores is essential for accurate spindle microtubule attachment.Mps1激酶向动粒的动态定位对于纺锤体微管的精确附着至关重要。
Proc Natl Acad Sci U S A. 2015 Aug 18;112(33):E4546-55. doi: 10.1073/pnas.1508791112. Epub 2015 Aug 3.
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A YAP/TAZ-induced feedback mechanism regulates Hippo pathway homeostasis.一种YAP/TAZ诱导的反馈机制调节Hippo信号通路的稳态。
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7
Centrosome-Associated Degradation Limits β-Catenin Inheritance by Daughter Cells after Asymmetric Division.中心体相关降解限制了β-连环蛋白在细胞不对称分裂后的子细胞中的遗传。
Curr Biol. 2015 Apr 20;25(8):1005-16. doi: 10.1016/j.cub.2015.02.020. Epub 2015 Mar 26.
8
Inefficient degradation of cyclin B1 re-activates the spindle checkpoint right after sister chromatid disjunction.细胞周期蛋白B1的降解效率低下会在姐妹染色单体分离后立即重新激活纺锤体检查点。
Cell Cycle. 2014;13(15):2370-8. doi: 10.4161/cc.29336.
9
Regulating the 20S proteasome ubiquitin-independent degradation pathway.调控20S蛋白酶体非泛素依赖性降解途径。
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10
Limiting the power of p53 through the ubiquitin proteasome pathway.通过泛素蛋白酶体途径限制 p53 的活性。
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局部消耗的益处:作为泛素-蛋白酶体介导降解支架的中心体

The benefits of local depletion: The centrosome as a scaffold for ubiquitin-proteasome-mediated degradation.

作者信息

Vora Setu M, Phillips Bryan T

机构信息

a Department of Biological Sciences, University of Iowa , Iowa City , IA , USA.

出版信息

Cell Cycle. 2016 Aug 17;15(16):2124-2134. doi: 10.1080/15384101.2016.1196306. Epub 2016 Jun 13.

DOI:10.1080/15384101.2016.1196306
PMID:27294844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4993542/
Abstract

The centrosome is the major microtubule-organizing center in animal cells but is dispensable for proper microtubule spindle formation in many biological contexts and is thus thought to fulfill additional functions. Recent observations suggest that the centrosome acts as a scaffold for proteasomal degradation in the cell to regulate a variety of biological processes including cell fate acquisition, cell cycle control, stress response, and cell morphogenesis. Here, we review the body of studies indicating a role for the centrosome in promoting proteasomal degradation of ubiquitin-proteasome substrates and explore the functional relevance of this system in different biological contexts. We discuss a potential role for the centrosome in coordinating local degradation of proteasomal substrates, allowing cells to achieve stringent spatiotemporal control over various signaling processes.

摘要

中心体是动物细胞中主要的微管组织中心,但在许多生物学环境中对于正确的微管纺锤体形成并非必需,因此被认为具有其他功能。最近的观察表明,中心体在细胞中作为蛋白酶体降解的支架,以调节多种生物学过程,包括细胞命运获得、细胞周期控制、应激反应和细胞形态发生。在这里,我们综述了一系列表明中心体在促进泛素-蛋白酶体底物的蛋白酶体降解中发挥作用的研究,并探讨了该系统在不同生物学环境中的功能相关性。我们讨论了中心体在协调蛋白酶体底物的局部降解中的潜在作用,使细胞能够对各种信号传导过程实现严格的时空控制。