The interplay between histone modifications and nuclear lamina in genome regulation

被引:1
作者
Sun, Chang [1 ,2 ]
Zhao, Yanjing [1 ,3 ]
Guo, Liping [1 ,4 ]
Qiu, Juhui [5 ]
Peng, Qin [1 ]
机构
[1] Shenzhen Bay Lab, Inst Syst & Phys Biol, Shenzhen 518132, Peoples R China
[2] Barcelona Univ, Fac Med & Hlth Sci, Barcelona, Spain
[3] Hong Kong Univ Sci & Technol, Div Life Sci, Clear Water Bay, Hong Kong, Peoples R China
[4] South China Univ Technol, Sch Biol & Biol Engn, Guangzhou 510006, Guangdong, Peoples R China
[5] Chongqing Univ, Coll Bioengn, Key Lab Biorheol Sci & Technol, State & Local Joint Engn Lab Vasc Implants,Minist, Chongqing 400030, Peoples R China
来源
JOURNAL OF GENETICS AND GENOMICS | 2025年 / 52卷 / 01期
基金
中国国家自然科学基金;
关键词
Histone modifications; Chromatin organization; Nuclear lamina; Lamina-associated domain; Genome regulation; Cell differentiation; RETT-SYNDROME; CHROMATIN; HETEROCHROMATIN; PROTEIN; ARCHITECTURE; TRANSCRIPTION; STEM; A/C; ORGANIZATION; ENVELOPE;
D O I
10.1016/j.jgg.2024.10.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene expression is regulated by chromatin architecture and epigenetic remodeling in cell homeostasis and pathologies. Histone modifications act as the key factors to modulate the chromatin accessibility. Different histone modifications are strongly associated with the localization of chromatin. Heterochromatin primarily localizes at the nuclear periphery, where it interacts with lamina proteins to suppress gene expression. In this review, we summarize the potential bridges that have regulatory functions of histone modifications in chromatin organization and transcriptional regulation at the nuclear periphery. We use lamina-associated domains (LADs) as examples to elucidate the biological roles of the interactions between histone modifications and nuclear lamina in cell differentiation and development. In the end, we highlight the technologies that are currently used to identify and visualize histone modifications and LADs, which could provide spatiotemporal information for understanding their regulatory functions in gene expression and discovering new targets for diseases. Copyright (c) 2024, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Limited and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:24 / 38
页数:15
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