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丢失、获得与保留:驱动减数第一次分裂前期晚期染色体重塑以实现精确减数分裂染色体分离的机制

Loss, Gain, and Retention: Mechanisms Driving Late Prophase I Chromosome Remodeling for Accurate Meiotic Chromosome Segregation.

作者信息

Láscarez-Lagunas Laura I, Martinez-Garcia Marina, Colaiácovo Monica P

机构信息

Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

Department of Biotechnology-Plant Biology, School of Agricultural, Food and Biosystems Engineering, Universidad Politécnica de Madrid, 28040 Madrid, Spain.

出版信息

Genes (Basel). 2022 Mar 19;13(3):546. doi: 10.3390/genes13030546.

DOI:10.3390/genes13030546
PMID:35328099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8949218/
Abstract

To generate gametes, sexually reproducing organisms need to achieve a reduction in ploidy, via meiosis. Several mechanisms are set in place to ensure proper reductional chromosome segregation at the first meiotic division (MI), including chromosome remodeling during late prophase I. Chromosome remodeling after crossover formation involves changes in chromosome condensation and restructuring, resulting in a compact bivalent, with sister kinetochores oriented to opposite poles, whose structure is crucial for localized loss of cohesion and accurate chromosome segregation. Here, we review the general processes involved in late prophase I chromosome remodeling, their regulation, and the strategies devised by different organisms to produce bivalents with configurations that promote accurate segregation.

摘要

为了产生配子,有性生殖生物需要通过减数分裂实现倍性的降低。有几种机制来确保在第一次减数分裂(MI)时染色体正确减数分离,包括在减数第一次分裂前期后期的染色体重塑。交叉形成后的染色体重塑涉及染色体凝聚和重组的变化,产生一个紧密的二价体,姐妹动粒朝向相反的极,其结构对于局部黏连丧失和准确的染色体分离至关重要。在这里,我们综述了减数第一次分裂前期后期染色体重塑所涉及的一般过程、它们的调控以及不同生物为产生具有促进准确分离构型的二价体而设计的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef98/8949218/9f1946f3cecb/genes-13-00546-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef98/8949218/9f1946f3cecb/genes-13-00546-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef98/8949218/9f1946f3cecb/genes-13-00546-g001.jpg

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本文引用的文献

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Proc Natl Acad Sci U S A. 2021 Apr 27;118(17). doi: 10.1073/pnas.2016363118.
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ZYP1 is required for obligate cross-over formation and cross-over interference in .ZYP1 对于 中必需的交叉形成和交叉干涉。
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The synaptonemal complex imposes crossover interference and heterochiasmy in .联会复合体在 中施加交叉干扰和异染色质。
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Phosphoregulation of HORMA domain protein HIM-3 promotes asymmetric synaptonemal complex disassembly in meiotic prophase in Caenorhabditis elegans.HORMA 结构域蛋白 HIM-3 的磷酸化调节促进了线虫减数分裂前期的不对称联会复合体的解聚。
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Multivalent weak interactions between assembly units drive synaptonemal complex formation.多价弱相互作用在组装单元之间驱动联会复合体的形成。
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