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小鼠减数分裂中的性别二态性。

Sexual Dimorphism in Mouse Meiosis.

作者信息

Hua Rong, Liu Mingxi

机构信息

State Key Laboratory of Reproductive Medicine, Department of Histology and Embryology, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, China.

出版信息

Front Cell Dev Biol. 2021 May 10;9:670599. doi: 10.3389/fcell.2021.670599. eCollection 2021.

DOI:10.3389/fcell.2021.670599
PMID:34041246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8141796/
Abstract

Meiosis is a highly conserved and essential process in gametogenesis in sexually reproducing organisms. However, there are substantial sex-specific differences within individual species with respect to meiosis-related chromatin reorganization, recombination, and tolerance for meiotic defects. A wide range of murine models have been developed over the past two decades to study the complex regulatory processes governing mammalian meiosis. The present review article thus provides a comprehensive overview of the knockout mice that have been employed to study meiosis, with a particular focus on gene- and gametogenesis-related sexual dimorphism observed in these model animals. In so doing, we aim to provide a firm foundation for the future study of sex-specific differences in meiosis at the molecular level.

摘要

减数分裂是有性生殖生物体配子发生过程中高度保守且必不可少的过程。然而,在减数分裂相关的染色质重组、重组以及对减数分裂缺陷的耐受性方面,单个物种内存在显著的性别特异性差异。在过去二十年中,已经开发了多种小鼠模型来研究控制哺乳动物减数分裂的复杂调控过程。因此,本综述文章全面概述了用于研究减数分裂的基因敲除小鼠,特别关注在这些模型动物中观察到的与基因和配子发生相关的性别二态性。通过这样做,我们旨在为未来在分子水平上研究减数分裂中的性别特异性差异提供坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1518/8141796/9eee5bd991ae/fcell-09-670599-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1518/8141796/746e9ff4a032/fcell-09-670599-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1518/8141796/9eee5bd991ae/fcell-09-670599-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1518/8141796/746e9ff4a032/fcell-09-670599-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1518/8141796/9eee5bd991ae/fcell-09-670599-g002.jpg

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1
Sexual Dimorphism in Mouse Meiosis.小鼠减数分裂中的性别二态性。
Front Cell Dev Biol. 2021 May 10;9:670599. doi: 10.3389/fcell.2021.670599. eCollection 2021.
2
Leagues of their own: sexually dimorphic features of meiotic prophase I.各自的联盟:减数分裂前期I的性别二态性特征
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Not all germ cells are created equal: aspects of sexual dimorphism in mammalian meiosis.并非所有生殖细胞都是相同的:哺乳动物减数分裂中的性别二态性方面。
Reproduction. 2005 Dec;130(6):761-81. doi: 10.1530/rep.1.00865.
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Sex-chromosome pairing and activity during mammalian meiosis.哺乳动物减数分裂过程中的性染色体配对与活性
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Mammalian meiotic silencing exhibits sexually dimorphic features.哺乳动物减数分裂沉默表现出性别二态性特征。
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The enigmatic meiotic dense body and its newly discovered component, SCML1, are dispensable for fertility and gametogenesis in mice.神秘的减数分裂致密体及其新发现的成分SCML1对小鼠的生育能力和配子发生并非必需。
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A mammal-specific Doublesex homolog associates with male sex chromatin and is required for male meiosis.一种哺乳动物特有的双性同源物与雄性性染色质相关联,是雄性减数分裂所必需的。
PLoS Genet. 2007 Apr 20;3(4):e62. doi: 10.1371/journal.pgen.0030062. Epub 2007 Mar 7.
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Mismatch repair proteins, meiosis, and mice: understanding the complexities of mammalian meiosis.错配修复蛋白、减数分裂与小鼠:理解哺乳动物减数分裂的复杂性
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Mammalian meiosis is more conserved by sex than by species: conserved co-expression networks of meiotic prophase.哺乳动物减数分裂的性别保守性高于物种保守性:减数分裂前期的保守共表达网络。
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本文引用的文献

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Mammalian germ cells are determined after PGC colonization of the nascent gonad.哺乳动物生殖细胞在原始性腺中被原始生殖细胞定植后就被决定了。
Proc Natl Acad Sci U S A. 2019 Dec 17;116(51):25677-25687. doi: 10.1073/pnas.1910733116. Epub 2019 Nov 21.
2
FBXO47 regulates telomere-inner nuclear envelope integration by stabilizing TRF2 during meiosis.FBXO47 通过在减数分裂过程中稳定 TRF2 来调节端粒-核内信封的整合。
Nucleic Acids Res. 2019 Dec 16;47(22):11755-11770. doi: 10.1093/nar/gkz992.
3
The histone modification reader ZCWPW1 is required for meiosis prophase I in male but not in female mice.
通过基于限制性片段连接的Refresh-seq技术对小鼠减数分裂重组的交叉事件进行定位。
Cell Discov. 2024 Mar 5;10(1):26. doi: 10.1038/s41421-023-00638-9.
4
Formation of Different Polyploids Through Disrupting Meiotic Crossover Frequencies Based on cntd1 Knockout in Zebrafish.基于 cntd1 基因敲除在斑马鱼中破坏减数分裂交叉频率形成不同的多倍体。
Mol Biol Evol. 2024 Mar 1;41(3). doi: 10.1093/molbev/msae047.
5
A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertility.两例原发不孕女性中 TERB1 蛋白截断变异的纯合子报告。
J Assist Reprod Genet. 2024 Mar;41(3):751-756. doi: 10.1007/s10815-024-03031-x. Epub 2024 Jan 26.
6
The arginine methyltransferase Prmt1 coordinates the germline arginine methylome essential for spermatogonial homeostasis and male fertility.精原干细胞中精氨酸甲基转移酶 Prmt1 调控的精氨酸甲基组学对于精原干细胞自我更新和雄性生育力至关重要。
Nucleic Acids Res. 2023 Oct 27;51(19):10428-10450. doi: 10.1093/nar/gkad769.
7
ApoC3 is expressed in oocytes and increased expression is associated with PCOS progression.载脂蛋白 C3 在卵母细胞中表达,其表达增加与 PCOS 的进展有关。
J Ovarian Res. 2023 Sep 9;16(1):188. doi: 10.1186/s13048-023-01263-6.
8
M1AP interacts with the mammalian ZZS complex and promotes male meiotic recombination.M1AP 与哺乳动物 ZZS 复合物相互作用,促进雄性减数分裂重组。
EMBO Rep. 2023 Feb 6;24(2):e55778. doi: 10.15252/embr.202255778. Epub 2022 Nov 28.
9
Chromosome Changes in Soma and Germ Line: Heritability and Evolutionary Outcome.体细胞和生殖系中的染色体变化:遗传性和进化结果。
Genes (Basel). 2022 Mar 28;13(4):602. doi: 10.3390/genes13040602.
组蛋白修饰读取蛋白 ZCWPW1 在雄性而非雌性小鼠减数分裂前期 I 中是必需的。
Sci Adv. 2019 Aug 14;5(8):eaax1101. doi: 10.1126/sciadv.aax1101. eCollection 2019 Aug.
4
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Elife. 2019 Feb 27;8:e43738. doi: 10.7554/eLife.43738.
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XRCC2 mutation causes meiotic arrest, azoospermia and infertility.XRCC2 突变导致减数分裂阻滞、无精子症和不育。
J Med Genet. 2018 Sep;55(9):628-636. doi: 10.1136/jmedgenet-2017-105145. Epub 2018 Jul 24.
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Meiosis: the chromosomal foundation of reproduction.减数分裂:生殖的染色体基础。
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Dual roles of TRF1 in tethering telomeres to the nuclear envelope and protecting them from fusion during meiosis.端粒结合蛋白 1 在将端粒锚定于核膜并在减数分裂过程中防止其融合中的双重作用。
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Proc Natl Acad Sci U S A. 2017 Nov 21;114(47):E10132-E10141. doi: 10.1073/pnas.1710837114. Epub 2017 Nov 6.
10
Telomeric TERB1-TRF1 interaction is crucial for male meiosis.端粒TERB1-TRF1相互作用对雄性减数分裂至关重要。
Nat Struct Mol Biol. 2017 Dec;24(12):1073-1080. doi: 10.1038/nsmb.3496. Epub 2017 Oct 30.