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减数分裂I中同源染色体的分离取决于分离酶对减数分裂黏连蛋白Rec8的蛋白水解切割。

Disjunction of homologous chromosomes in meiosis I depends on proteolytic cleavage of the meiotic cohesin Rec8 by separin.

作者信息

Buonomo S B, Clyne R K, Fuchs J, Loidl J, Uhlmann F, Nasmyth K

机构信息

Research Institute of Molecular Pathology, University of Vienna, Austria.

出版信息

Cell. 2000 Oct 27;103(3):387-98. doi: 10.1016/s0092-8674(00)00131-8.

Abstract

It has been proposed but never proven that cohesion between sister chromatids distal to chiasmata is responsible for holding homologous chromosomes together while spindles attempt to pull them toward opposite poles during metaphase of meiosis I. Meanwhile, the mechanism by which disjunction of homologs is triggered at the onset of anaphase I has remained a complete mystery. In yeast, cohesion between sister chromatid arms during meiosis depends on a meiosis-specific cohesin subunit called Rec8, whose mitotic equivalent, Sccl, is cleaved at the metaphase to anaphase transition by an endopeptidase called separin. We show here that cleavage of Rec8 by separin at one of two different sites is necessary for the resolution of chiasmata and the disjunction of homologous chromosomes during meiosis.

摘要

有人提出,但从未得到证实,在减数分裂I中期,当纺锤体试图将同源染色体拉向相反两极时,交叉远端的姐妹染色单体之间的黏连负责将同源染色体维系在一起。同时,在减数分裂I后期开始时触发同源染色体分离的机制仍然完全是个谜。在酵母中,减数分裂期间姐妹染色单体臂之间的黏连依赖于一种名为Rec8的减数分裂特异性黏连蛋白亚基,其在有丝分裂中的对应物Sccl在中期到后期转换时被一种名为分离酶的内肽酶切割。我们在此表明,分离酶在两个不同位点之一对Rec8的切割对于减数分裂期间交叉的解决和同源染色体的分离是必要的。

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