粘蛋白
姐妹染色单体
分离酶
生物
减数分裂
姐妹染色单体结合力的建立
减数分裂II
动细胞
染色体分离
后期
细胞生物学
劈理(地质)
遗传学
染色体
基因
古生物学
断裂(地质)
作者
Sugako Ogushi,Ahmed Rattani,Jonathan Godwin,Jean Metson,Lothar Schermelleh,K Nasmyth
标识
DOI:10.1016/j.devcel.2021.10.017
摘要
Protection of peri-centromeric (periCEN) REC8 cohesin from Separase and sister kinetochore (KT) attachment to microtubules emanating from the same spindle pole (co-orientation) ensures that sister chromatids remain associated after meiosis I. Both features are lost during meiosis II, resulting in sister chromatid disjunction and the production of haploid gametes. By transferring spindle-chromosome complexes (SCCs) between meiosis I and II in mouse oocytes, we discovered that both sister KT co-orientation and periCEN cohesin protection depend on the SCC, and not the cytoplasm. Moreover, the catalytic activity of Separase at meiosis I is necessary not only for converting KTs from a co- to a bi-oriented state but also for deprotection of periCEN cohesion, and cleavage of REC8 may be the key event. Crucially, selective cleavage of REC8 in the vicinity of KTs is sufficient to destroy co-orientation in univalent chromosomes, albeit not in bivalents where resolution of chiasmata may also be required
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