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秀丽隐杆线虫减数分裂I前期的染色体运动

Chromosome movement in meiosis I prophase of Caenorhabditis elegans.

作者信息

Woglar Alexander, Jantsch Verena

机构信息

Department of Chromosome Biology, Max F. Perutz Laboratories, University of Vienna, Dr.-Bohrgasse 9, 1030, Vienna, Austria.

出版信息

Chromosoma. 2014 Mar;123(1-2):15-24. doi: 10.1007/s00412-013-0436-7. Epub 2013 Sep 15.

DOI:10.1007/s00412-013-0436-7
PMID:24036686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3967079/
Abstract

Rapid chromosome movement during prophase of the first meiotic division has been observed in many organisms. It is generally concomitant with formation of the "meiotic chromosome bouquet," a special chromosome configuration in which one or both chromosome ends attach to the nuclear envelope and become concentrated within a limited area. The precise function of the chromosomal bouquet is still not fully understood. Chromosome mobility is implicated in homologous chromosome pairing, synaptonemal complex formation, recombination, and resolution of chromosome entanglements. The basic mechanistic module through which forces are exerted on chromosomes is widely conserved; however, phenotypic differences have been reported among various model organisms once movement is abrogated. Movements are transmitted to the chromosome ends by the nuclear membrane-bridging SUN/KASH complex and are dependent on cytoskeletal filaments and motor proteins located in the cytoplasm. Here we review the recent findings on chromosome mobility during meiosis in an animal model system: the Caenorhabditis elegans nematode.

摘要

在许多生物体中都观察到了第一次减数分裂前期染色体的快速移动。它通常与“减数分裂染色体花束”的形成相伴,“减数分裂染色体花束”是一种特殊的染色体构型,其中一个或两个染色体末端附着于核膜并集中在一个有限的区域内。染色体花束的确切功能仍未完全了解。染色体移动与同源染色体配对、联会复合体形成、重组以及染色体缠结的解决有关。对染色体施加力的基本机制模块广泛保守;然而,一旦移动被消除,在各种模式生物中已报道了表型差异。移动通过核膜桥接的SUN/KASH复合体传递到染色体末端,并依赖于位于细胞质中的细胞骨架细丝和马达蛋白。在此,我们综述了动物模型系统(秀丽隐杆线虫)减数分裂期间染色体移动的最新研究结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/7c346139e3b7/412_2013_436_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/c3cc37e0b73a/412_2013_436_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/9eac8f0ea978/412_2013_436_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/f1badf813351/412_2013_436_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/d06dac2c6762/412_2013_436_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/7c346139e3b7/412_2013_436_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/c3cc37e0b73a/412_2013_436_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/9eac8f0ea978/412_2013_436_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/f1badf813351/412_2013_436_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/d06dac2c6762/412_2013_436_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec5e/3967079/7c346139e3b7/412_2013_436_Fig5_HTML.jpg

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PLoS Genet. 2013 May;9(5):e1003497. doi: 10.1371/journal.pgen.1003497. Epub 2013 May 9.
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