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2
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本文引用的文献

1
Implications for Diverse Functions of the LINC Complexes Based on the Structure.基于结构对LINC复合体多种功能的启示
Cells. 2017 Jan 26;6(1):3. doi: 10.3390/cells6010003.
2
Regulating chromosomal movement by the cochaperone FKB-6 ensures timely pairing and synapsis.伴侣蛋白FKB-6调控染色体运动以确保适时配对和联会。
J Cell Biol. 2017 Feb;216(2):393-408. doi: 10.1083/jcb.201606126. Epub 2017 Jan 11.
3
Speedy A-Cdk2 binding mediates initial telomere-nuclear envelope attachment during meiotic prophase I independent of Cdk2 activation.快速的A-Cdk2结合介导减数分裂前期I期间端粒与核膜的初始附着,且不依赖于Cdk2激活。
Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):592-597. doi: 10.1073/pnas.1618465114. Epub 2016 Dec 28.
4
LINC complexes promote homologous recombination in part through inhibition of nonhomologous end joining.LINC复合物部分通过抑制非同源末端连接来促进同源重组。
J Cell Biol. 2016 Dec 19;215(6):801-821. doi: 10.1083/jcb.201604112. Epub 2016 Dec 12.
5
Meiotic Nuclear Oscillations Are Necessary to Avoid Excessive Chromosome Associations.减数分裂核振荡对于避免过度的染色体关联是必要的。
Cell Rep. 2016 Nov 1;17(6):1632-1645. doi: 10.1016/j.celrep.2016.10.014.
6
Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelope.细胞周期蛋白依赖性激酶2激活因子RingoA在减数分裂端粒与核膜连接中的重要作用。
Nat Commun. 2016 Mar 30;7:11084. doi: 10.1038/ncomms11084.
7
MAJIN Links Telomeric DNA to the Nuclear Membrane by Exchanging Telomere Cap.MAJIN 通过交换端粒帽将端粒 DNA 与核膜联系起来。
Cell. 2015 Nov 19;163(5):1252-1266. doi: 10.1016/j.cell.2015.10.030. Epub 2015 Nov 5.
8
Microtubule-driven nuclear rotations promote meiotic chromosome dynamics.微管驱动的核旋转促进了减数分裂染色体的动力学行为。
Nat Cell Biol. 2015 Nov;17(11):1388-400. doi: 10.1038/ncb3249. Epub 2015 Oct 12.
9
Recombination, Pairing, and Synapsis of Homologs during Meiosis.减数分裂过程中同源染色体的重组、配对和联会
Cold Spring Harb Perspect Biol. 2015 May 18;7(6):a016626. doi: 10.1101/cshperspect.a016626.
10
Mechanism and regulation of rapid telomere prophase movements in mouse meiotic chromosomes.小鼠减数分裂染色体中端粒前期快速运动的机制与调控
Cell Rep. 2015 Apr 28;11(4):551-63. doi: 10.1016/j.celrep.2015.03.045. Epub 2015 Apr 16.

运动和停止:调控染色体运动以促进减数分裂染色体配对和联会。

Moving and stopping: Regulation of chromosome movement to promote meiotic chromosome pairing and synapsis.

机构信息

a Department of Biology , The University of Iowa , Iowa City, IA , USA.

出版信息

Nucleus. 2017 Nov 2;8(6):613-624. doi: 10.1080/19491034.2017.1358329. Epub 2017 Sep 11.

DOI:10.1080/19491034.2017.1358329
PMID:28892406
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5788555/
Abstract

Meiosis is a specialized cellular division occurring in organisms capable of sexual reproduction that leads to the formation of gametes containing half of the original chromosome number. During the earliest stage of meiosis, prophase I, pairing of homologous chromosomes is achieved in preparation for their proper distribution in the coming divisions. An important question is how do homologous chromosomes find each other and establish pairing interactions. Early studies demonstrated that chromosomes are dynamic in nature and move during this early stage of meiosis. More recently, there have been several studies across different models showing the conserved nature and importance of this chromosome movement, as well as the key components involved in chromosome movement. This review will cover these major findings and also introduce unexamined areas of regulation in meiotic prophase I chromosome movement.

摘要

减数分裂是一种在有性生殖能力的生物体中发生的特殊细胞分裂,导致配子形成,其中包含原始染色体数目的一半。在减数分裂的最早阶段,前期 I 中,同源染色体的配对是在为即将到来的分裂中正确分配做准备。一个重要的问题是同源染色体如何相互找到并建立配对相互作用。早期的研究表明,染色体在本质上是动态的,并在减数分裂的早期阶段移动。最近,在不同的模型中进行了几项研究,显示了这种染色体运动的保守性质和重要性,以及参与染色体运动的关键成分。本综述将涵盖这些主要发现,并介绍减数分裂前期 I 染色体运动中未被研究的调控领域。