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评估成熟精子中组蛋白的定位和DNA结合复杂性。

Evaluating the localization and DNA binding complexity of histones in mature sperm.

作者信息

Miller David, Paradowska Agnieszka

机构信息

Leeds Institute of Genetics, Health and Therapeutics, University of Leeds, Leeds, West Yorkshire, UK.

出版信息

Methods Mol Biol. 2013;927:459-75. doi: 10.1007/978-1-62703-038-0_40.

Abstract

The paternal genome in many animal taxa is efficiently packaged into the sperm nucleus by switching from a histone (nucleosome)-based chromatin configuration to one using predominantly protamines. Nonetheless, various studies have shown that some nucleosomes, often containing modified histones are retained in mature sperm and bind DNA with distinct sequence compositions. Considering the significance of histone modifications in epigenetic phenomena and the fact that sperm histones and their bound DNA must be carried into the oocyte, this chapter describes methods aimed at examining and analysing the histone composition of sperm chromatin. The focus is on both microscopic visualisation and evaluation of sequence composition of histones and histone-bound DNA in human and mouse spermatozoa. However, similar methods may be applicable to the sperm of other mammalian and even non-mammalian classes.

摘要

在许多动物类群中,父本基因组通过从基于组蛋白(核小体)的染色质构型转变为主要使用鱼精蛋白的构型,从而有效地包装到精子细胞核中。尽管如此,各种研究表明,一些通常含有修饰组蛋白的核小体保留在成熟精子中,并与具有不同序列组成的DNA结合。鉴于组蛋白修饰在表观遗传现象中的重要性,以及精子组蛋白及其结合的DNA必须被带入卵母细胞这一事实,本章描述了旨在检测和分析精子染色质组蛋白组成的方法。重点是对人类和小鼠精子中组蛋白及组蛋白结合DNA的序列组成进行显微镜观察和评估。然而,类似的方法可能适用于其他哺乳动物甚至非哺乳动物类群的精子。

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