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Meiotic Cohesin Promotes Pairing of Nonhomologous Centromeres in Early Meiotic Prophase

机译:减数分裂黏附素促进减数分裂前期的非同源着丝粒配对。

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摘要

A period of pairing between nonhomologous centromeres occurs early in meiosis in a diverse collection of organisms. This early, homology-independent, centromere pairing, referred to as centromere coupling in budding yeast, gives way to an alignment of homologous centromeres as homologues synapse later in meiotic prophase. The regulation of centromere coupling and its underlying mechanism have not been elucidated. In budding yeast, the protein Zip1p is a major component of the central element of the synaptonemal complex in pachytene of meiosis, and earlier, is essential for centromere coupling. The experiments reported here demonstrate that centromere coupling is mechanistically distinct from synaptonemal complex assembly. Zip2p, Zip3p, and Red1p are all required for the assembly of Zip1 into the synaptonemal complex but are dispensable for centromere coupling. However, the meiotic cohesin Rec8p is required for centromere coupling. Loading of meiotic cohesins to centromeres and cohesin-associated regions is required for the association of Zip1 with these sites, and the association of Zip1 with the centromeres then promotes coupling. These findings reveal a mechanism that promotes associations between centromeres before the assembly of the synaptonemal complex, and they demonstrate that chromosomes are preloaded with Zip1p in a manner that may promote synapsis.
机译:非同源着丝粒之间的配对期发生在减数分裂早期的多种生物中。这种早期的,不依赖同源性的着丝粒配对,即发芽酵母中的着丝粒偶联,让位于同源着丝粒的比对,后者是减数分裂前期的同源突触。着丝粒耦合的调控及其潜在机制尚未阐明。在发芽的酵母中,蛋白Zip1p是减数分裂的粗线期中突触复合物中心成分的主要成分,并且更早地是着丝粒耦合所必需的。此处报道的实验表明着丝粒耦合在机制上不同于突触复合体装配。 Zip1p组装到联会复合物中都需要Zip2p,Zip3p和Red1p,但它们对于着丝粒耦合是必不可少的。但是,减数分裂粘附素Rec8p是着丝粒偶联所必需的。 Zip1与这些位点的关联需要减数分裂黏附素加载到着丝粒和与黏着素相关的区域,然后Zip1与着丝粒的关联会促进偶联。这些发现揭示了在突触复合体组装之前促进着丝粒之间的缔合的机制,并且它们表明染色体以可能促进突触的方式预载了Zip1p。

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