减数分裂调控Ndc80复合体的组成和功能。

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY
Current Genetics Pub Date : 2021-08-01 Epub Date: 2021-03-21 DOI:10.1007/s00294-021-01174-3
Jingxun Chen, Elçin Ünal
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引用次数: 2

摘要

这篇综述描述了Ndc80复合物亚基丰度是如何在出芽酵母和后生动物减数分裂中调控的。Ndc80复合物是一个关键的着丝点成分。过去几十年的着丝点研究已经确定Ndc80复合体是一个关键的微管相互作用因子和调节染色体分离的中心枢纽。最近的研究进一步表明,Ndc80是芽殖酵母减数分裂中决定着丝粒激活时间的限制性着丝粒亚基。本文讨论了出芽酵母减数分裂过程中调控Ndc80蛋白合成和降解的分子回路,并与后生动物的研究结果进行了比较。我们设想在出芽酵母中发现的调节原理在后生动物中保守,从而为未来研究着丝点在人类健康和疾病中的调节提供指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Meiotic regulation of the Ndc80 complex composition and function.

Meiotic regulation of the Ndc80 complex composition and function.

This review describes the current models for how the subunit abundance of the Ndc80 complex, a key kinetochore component, is regulated in budding yeast and metazoan meiosis. The past decades of kinetochore research have established the Ndc80 complex to be a key microtubule interactor and a central hub for regulating chromosome segregation. Recent studies further demonstrate that Ndc80 is the limiting kinetochore subunit that dictates the timing of kinetochore activation in budding yeast meiosis. Here, we discuss the molecular circuits that regulate Ndc80 protein synthesis and degradation in budding yeast meiosis and compare the findings with those from metazoans. We envision the regulatory principles discovered in budding yeast to be conserved in metazoans, thereby providing guidance into future investigations on kinetochore regulation in human health and disease.

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来源期刊
Current Genetics
Current Genetics 生物-遗传学
CiteScore
6.00
自引率
0.00%
发文量
34
审稿时长
1 months
期刊介绍: Current Genetics publishes genetic, genomic, molecular and systems-level analysis of eukaryotic and prokaryotic microorganisms and cell organelles. All articles are peer-reviewed. The journal welcomes submissions employing any type of research approach, be it analytical (aiming at a better understanding), applied (aiming at practical applications), synthetic or theoretical. Current Genetics no longer accepts manuscripts describing the genome sequence of mitochondria/chloroplast of a small number of species. Manuscripts covering sequence comparisons and analyses that include a large number of species will still be considered.
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