敲除故事:组蛋白H3.3在发育和疾病中的多功能作用。

IF 4.2 2区 生物学 Q1 GENETICS & HEREDITY
Rachel H Klein, Paul S Knoepfler
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引用次数: 0

摘要

与典型H3蛋白相比,组蛋白变体H3.3在发育中发挥着新的作用,并且是人类疾病中最常见的突变组蛋白。在这里,我们讨论了两个H3.3编码基因H3f3a和H3f3b的基因靶向研究如何为H3.3的功能提供了重要的见解,包括配子以及大脑和肺部发育。敲除还深入了解了H3.3在维持基因组稳定性和染色质组织方面的重要作用,当H3.3在儿童肿瘤和神经发育综合征等人类疾病中突变时,这些过程也会受到影响。总的来说,H3.3是一种独特的组蛋白,通过表观基因组机制将发育和疾病联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Knockout tales: the versatile roles of histone H3.3 in development and disease.

Knockout tales: the versatile roles of histone H3.3 in development and disease.

Histone variant H3.3 plays novel roles in development as compared to canonical H3 proteins and is the most commonly mutated histone protein of any kind in human disease. Here we discuss how gene targeting studies of the two H3.3-coding genes H3f3a and H3f3b have provided important insights into H3.3 functions including in gametes as well as brain and lung development. Knockouts have also provided insights into the important roles of H3.3 in maintaining genomic stability and chromatin organization, processes that are also affected when H3.3 is mutated in human diseases such as pediatric tumors and neurodevelopmental syndromes. Overall, H3.3 is a unique histone linking development and disease via epigenomic machinery.

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来源期刊
Epigenetics & Chromatin
Epigenetics & Chromatin GENETICS & HEREDITY-
CiteScore
7.00
自引率
0.00%
发文量
35
审稿时长
1 months
期刊介绍: Epigenetics & Chromatin is a peer-reviewed, open access, online journal that publishes research, and reviews, providing novel insights into epigenetic inheritance and chromatin-based interactions. The journal aims to understand how gene and chromosomal elements are regulated and their activities maintained during processes such as cell division, differentiation and environmental alteration.
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