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Cytoskeletal Forces Span the Nuclear Envelope to Coordinate Meiotic Chromosome Pairing and Synapsis

机译:跨核包膜的细胞骨架力协调减数分裂染色体配对和突触。

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摘要

During meiosis, each chromosome must pair with its unique homologous partner, a process that usually culminates with the formation of the synaptonemal complex (SC). In the nematode Caenorhabditis elegans, special regions on each chromosome known as pairing centers are essential for both homologous pairing and synapsis. We report that during early meiosis, pairing centers establish transient connections to the cytoplasmic microtubule network. These connections through the intact nuclear envelope require the SUN/KASH domain protein pair SUN-1 and ZYG-12. Disruption of microtubules inhibits chromosome pairing, indicating that these connections promote interhomolog interactions. Dynein activity is essential to license formation of the SC once pairing has been accomplished, most likely by overcoming a barrier imposed by the chromosome-nuclear envelope connection. Our findings thus provide insight into how homolog pairing is accomplished in meiosis and into the mechanisms regulating synapsis so that it occurs selectively between homologs. For a video summary of this article, see the PaperFlick file with the Supplemental Data available online.
机译:在减数分裂过程中,每个染色体都必须与其独特的同源伴侣配对,这一过程通常以突触复合物(SC)的形成达到顶点。在线虫秀丽隐杆线虫中,每个染色体上称为配对中心的特殊区域对于同源配对和突触都是必不可少的。我们报告说,在减数分裂的早期,配对中心建立了到细胞质微管网络的瞬时连接。这些通过完整核膜的连接需要SUN / KASH域蛋白对SUN-1和ZYG-12。微管的破裂抑制了染色体配对,表明这些连接促进了同源物之间的相互作用。配对完成后,动力蛋白的活性对于SC的许可形成至关重要,很可能是通过克服染色体-核包膜连接所施加的障碍。因此,我们的发现为深入了解减数分裂中的同源物配对如何完成以及调节突触的机制提供了见识,从而使突触选择性地发生在同源物之间。有关本文的视频摘要,请参见在线提供补充数据的PaperFlick文件。

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