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首页> 外文期刊>Current Genetics: Eukaryotes with Emphasis on Yeasts, Fungi, Mitochondria, Plastids >An interplay between Shugoshin and Spo13 for centromeric cohesin protection and sister kinetochore mono-orientation during meiosis I in Saccharomyces cerevisiae
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An interplay between Shugoshin and Spo13 for centromeric cohesin protection and sister kinetochore mono-orientation during meiosis I in Saccharomyces cerevisiae

机译:Shugcaromyces Cerevisiae中舒科尼蛋白保护和姐妹Kinetochore单对思维的曙光尼蛋白保护与妹妹Kinetochore单对思维相互作用

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摘要

Meiosis is a specialized cell division process by which haploid gametes are produced from a diploid mother cell. Reductional chromosome segregation during meiosis I (MI) is achieved by two unique and conserved events: centromeric cohesin protection (CCP) and sister kinetochore mono-orientation (SKM). In Saccharomyces cerevisiae, a meiosis-specific protein Spo13 plays a role in both these centromere-specific events. Despite genome-wide association of Spo13, we failed to detect its function in global processes such as cohesin loading, cohesion establishment and homologs pairing. While Shugoshin (Sgo1) and protein phosphatase 2A (PP2A(Rts1)) play a central role in CCP, it is not fully understood whether Spo13 functions in the process through a Sgo1- PP2A(Rts1)-dependent or -independent mechanism. To delineate this and to find the relative contribution of each of these proteins in CCP and SKM, we meticulously observed the sister chromatid segregation pattern in the wild type, sgo1, rts1 and spo13 single mutants and in their respective double mutants. We found that Spo13 protects centromeric cohesin through a Sgo1- PP2A(Rts1)-independent mechanism. To our surprise, we observed a hitherto unknown role of Sgo1 in SKM. Further investigation revealed that Sgo1-mediated recruitment of aurora kinase Ipl1 to the centromere facilitates monopolin loading at the kinetochore during MI. Hence, this study uncovers the role of Sgo1 in SKM and demonstartes how the regulators (Sgo1, PP2A(Rts1), Spo13) work in a coordinated manner to achieve faithful chromosome segregation during meiosis, the failure of which leads to aneuploidy and birth defects.
机译:MeIosis是一种专用细胞分裂过程,通过哪个单倍体配子由二倍体母细胞产生。减少染色体染色体的染色体隔层(MI)是通过两个独特和保守的事件实现的:浓缩咖啡保护(CCP)和姐妹Kinetochore单向(SKM)。在酿酒酵母中,特异性特异性蛋白质SPO13在这些Centromere的特定事件中起着作用。尽管SPO13的基因组协会,但我们未能检测到其在池内装载,凝聚力建立和同源物配对等全局过程中的功能。虽然Shugoshin(Sgo1)和蛋白质磷酸酶2a(pp2a(rts1))在CCP中发挥着中心作用,但是在通过Sgo1-PP2A(RTS1) - 依赖性或依赖性机制中,不完全理解SPO13是否在该过程中起作用。为了描绘它并找到CCP和SKM中每种蛋白质的相对贡献,我们在野生型,SGO1,RTS1和SPO13单突变体中和它们各自的双突变体中精心观察到姐妹染色体偏析模式。我们发现Spo13通过Sgo1-PP2A(RTS1) - 依赖性机制来保护焦粒子。令我们惊讶的是,我们观察了SGO1在SKM中Sgo1的迄今为止的作用。进一步调查显示,Sgo1介导的Aurora激酶IPL1对Centromere的招募促进MI期间在Kinetochore的单调载荷。因此,本研究揭示了SGO1在SKM和演示术中的作用,该调节剂(SGO1,PP2A(RTS1),SPO13)以协调的方式工作,以实现在减数分裂中的忠实染色体隔离,其失败导致交通倍性和出生缺陷。

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