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减数分裂性染色体失活的染色体铺展分析

Chromosome Spread Analyses of Meiotic Sex Chromosome Inactivation.

作者信息

Alavattam Kris G, Abe Hironori, Sakashita Akihiko, Namekawa Satoshi H

机构信息

Division of Reproductive Sciences, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

出版信息

Methods Mol Biol. 2018;1861:113-129. doi: 10.1007/978-1-4939-8766-5_10.

DOI:10.1007/978-1-4939-8766-5_10
PMID:30218364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8243718/
Abstract

A distinct form of X chromosome inactivation takes place during male meiosis, when the male sex chromosomes undergo a phenomenon known as meiotic sex chromosome inactivation (MSCI). MSCI is directed by DNA damage response signaling independent of Xist RNA to silence the transcriptional activity of the sex chromosomes, an essential event in male germ cell development. Here, we present protocols for the preparation and analyses of chromosome spread slides of mouse meiotic spermatocytes, thereby enabling a quick, inexpensive, and powerful cytological method to complement gene expression studies.

摘要

一种独特的X染色体失活形式发生在雄性减数分裂过程中,此时雄性性染色体经历一种称为减数分裂性染色体失活(MSCI)的现象。MSCI由独立于Xist RNA的DNA损伤反应信号传导引导,以沉默性染色体的转录活性,这是雄性生殖细胞发育中的一个重要事件。在这里,我们展示了用于制备和分析小鼠减数分裂精母细胞染色体铺展玻片的方案,从而提供一种快速、廉价且强大的细胞学方法来补充基因表达研究。

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Chromosome Spread Analyses of Meiotic Sex Chromosome Inactivation.减数分裂性染色体失活的染色体铺展分析
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Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications.减数分裂中范可尼贫血蛋白网络的解析及其在组蛋白修饰调控中的作用
Cell Rep. 2016 Oct 18;17(4):1141-1157. doi: 10.1016/j.celrep.2016.09.073.
2
FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis.FANCB在雄性生殖细胞系中至关重要,并在减数分裂过程中调节性染色体上的H3K9甲基化。
Hum Mol Genet. 2015 Sep 15;24(18):5234-49. doi: 10.1093/hmg/ddv244. Epub 2015 Jun 29.
3
BAZ1B is dispensable for H2AX phosphorylation on Tyrosine 142 during spermatogenesis.
CTCF介导的三维染色质构建雄性生殖系中的基因表达程序。
Nat Struct Mol Biol. 2025 Mar 3. doi: 10.1038/s41594-025-01482-z.
4
hnRNPC Functions with HuR to Regulate Alternative Splicing in an m6A-Dependent Manner and is Essential for Meiosis.异质性核糖核蛋白C(hnRNPC)与HuR共同发挥作用,以m6A依赖的方式调节可变剪接,并且对减数分裂至关重要。
Adv Sci (Weinh). 2025 Apr;12(13):e2412196. doi: 10.1002/advs.202412196. Epub 2025 Feb 8.
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METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis.减数分裂性染色体失活以及雄性减数分裂期间双链断裂形成和重组需要METTL16
Adv Sci (Weinh). 2025 Jan;12(3):e2406332. doi: 10.1002/advs.202406332. Epub 2024 Nov 28.
6
Meiotic chromatin-associated HSF5 is indispensable for pachynema progression and male fertility.减数分裂染色质相关的 HSF5 对于粗线期进展和雄性育性是必不可少的。
Nucleic Acids Res. 2024 Sep 23;52(17):10255-10275. doi: 10.1093/nar/gkae701.
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A TOPBP1 allele causing male infertility uncouples XY silencing dynamics from sex body formation.一种导致男性不育的 TOPBP1 等位基因使 XY 沉默动力学与性体形成脱耦。
Elife. 2024 Feb 23;12:RP90887. doi: 10.7554/eLife.90887.
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