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Rec8磷酸化和重组促进减数分裂中黏连蛋白的逐步丢失。

Rec8 phosphorylation and recombination promote the step-wise loss of cohesins in meiosis.

作者信息

Brar Gloria A, Kiburz Brendan M, Zhang Yi, Kim Ji-Eun, White Forest, Amon Angelika

机构信息

Center for Cancer Research, Howard Hughes Medical Institute, Massachusetts Institute of Technology, E17-233 40 Ames Street, Cambridge, Massachusetts 02139, USA.

出版信息

Nature. 2006 May 25;441(7092):532-6. doi: 10.1038/nature04794. Epub 2006 May 3.

Abstract

During meiosis, cohesins--protein complexes that hold sister chromatids together--are lost from chromosomes in a step-wise manner. Loss of cohesins from chromosome arms is necessary for homologous chromosomes to segregate during meiosis I. Retention of cohesins around centromeres until meiosis II is required for the accurate segregation of sister chromatids. Here we show that phosphorylation of the cohesin subunit Rec8 contributes to step-wise cohesin removal. Our data further implicate two other key regulators of meiotic chromosome segregation, the cohesin protector Sgo1 and meiotic recombination in bringing about the step-wise loss of cohesins and thus the establishment of the meiotic chromosome segregation pattern. Understanding the interplay between these processes should provide insight into the events underlying meiotic chromosome mis-segregation, the leading cause of miscarriages and mental retardation in humans.

摘要

在减数分裂过程中,黏连蛋白(将姐妹染色单体结合在一起的蛋白质复合物)会以逐步的方式从染色体上消失。染色体臂上黏连蛋白的缺失是同源染色体在减数分裂I期间分离所必需的。着丝粒周围的黏连蛋白保留到减数分裂II对于姐妹染色单体的准确分离是必需的。在这里,我们表明黏连蛋白亚基Rec8的磷酸化有助于黏连蛋白的逐步去除。我们的数据进一步表明,减数分裂染色体分离的另外两个关键调节因子,即黏连蛋白保护因子Sgo1和减数分裂重组,导致了黏连蛋白的逐步丢失,从而建立了减数分裂染色体分离模式。了解这些过程之间的相互作用应该有助于深入了解减数分裂染色体错误分离背后的事件,而减数分裂染色体错误分离是人类流产和智力迟钝的主要原因。

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