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雄性生殖细胞分化的表观遗传调控。

Epigenetic regulation of male germ cell differentiation.

作者信息

Meikar Oliver, Da Ros Matteo, Kotaja Noora

机构信息

Institute of Biomedicine, Department of Physiology, University of Turku, Kiinamyllynkatu 10, Turku, FIN-20520, Finland.

出版信息

Subcell Biochem. 2013;61:119-38. doi: 10.1007/978-94-007-4525-4_6.

Abstract

Male germ cell differentiation is a complex developmental program that produces highly specialized mature spermatozoa capable of independent movement and fertilization of an egg. Germ cells are unique in their capability to generate new organisms, and extra caution has to be taken to secure the correct inheritance of genetic and epigenetic information. Male germ cells are epigenetically distinct from somatic cells and they undergo several important epigenetic transitions. In primordial germ cells (PGCs), epigenome is reprogrammed by genome-wide resetting of epigenetic marks, including the sex-specific imprinting of certain genes. Postnatal spermatogenesis is characterized by drastic chromatin rearrangements during meiotic recombination, sex chromosome silencing, and compaction of sperm nuclei, which is accomplished by replacing near to all histones by sperm-specific protamines. Small RNAs, including microRNAs (miRNAs), endogenous small interfering RNAs (endo-siRNAs) and PIWI-interacting RNAs (piRNAs) are also involved in the control of male gamete production. The activities of small RNAs in male germ cells are diverse, and include miRNA- and endo-siRNA-mediated posttranscriptional mRNA regulation and piRNA-driven transposon silencing and the control of DNA methylation in PGCs. In this chapter, we give a brief review on the epigenetic processes that govern chromatin organization and germline-specific gene expression in differentiating male germ cells.

摘要

雄性生殖细胞分化是一个复杂的发育过程,可产生具有高度特异性的成熟精子,这些精子能够自主移动并使卵子受精。生殖细胞在产生新生物体的能力方面具有独特性,因此必须格外谨慎以确保遗传和表观遗传信息的正确遗传。雄性生殖细胞在表观遗传学上与体细胞不同,它们会经历几个重要的表观遗传转变。在原始生殖细胞(PGC)中,表观基因组通过全基因组范围内表观遗传标记的重置进行重编程,包括某些基因的性别特异性印记。出生后精子发生的特征是在减数分裂重组、性染色体沉默和精子核压缩过程中发生剧烈的染色质重排,这是通过用精子特异性鱼精蛋白几乎取代所有组蛋白来实现的。小RNA,包括微小RNA(miRNA)、内源性小干扰RNA(endo-siRNA)和PIWI相互作用RNA(piRNA)也参与雄性配子产生的控制。小RNA在雄性生殖细胞中的活性多种多样,包括miRNA和endo-siRNA介导的转录后mRNA调控以及piRNA驱动的转座子沉默和PGC中DNA甲基化的控制。在本章中,我们简要回顾了在分化的雄性生殖细胞中控制染色质组织和生殖系特异性基因表达的表观遗传过程。

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