染色质
核小体
连接器DNA
组蛋白修饰酶
组蛋白
细胞生物学
组蛋白H1
染色体
化学
组蛋白八聚体
染色质重塑
组蛋白密码
生物
连接器
生物物理学
遗传学
DNA
组蛋白甲基化
基因
DNA甲基化
基因表达
计算机科学
操作系统
作者
Dmitry V. Fyodorov,Bing‐Rui Zhou,Arthur I. Skoultchi,Yawen Bai
摘要
Together with core histones, which make up the nucleosome, the linker histone (H1) is one of the five main histone protein families present in chromatin in eukaryotic cells. H1 binds to the nucleosome to form the next structural unit of metazoan chromatin, the chromatosome, which may help chromatin to fold into higher-order structures. Despite their important roles in regulating the structure and function of chromatin, linker histones have not been studied as extensively as core histones. Nevertheless, substantial progress has been made recently. The first near-atomic resolution crystal structure of a chromatosome core particle and an 11 Å resolution cryo-electron microscopy-derived structure of the 30 nm nucleosome array have been determined, revealing unprecedented details about how linker histones interact with the nucleosome and organize higher-order chromatin structures. Moreover, several new functions of linker histones have been discovered, including their roles in epigenetic regulation and the regulation of DNA replication, DNA repair and genome stability. Studies of the molecular mechanisms of H1 action in these processes suggest a new paradigm for linker histone function beyond its architectural roles in chromatin.
科研通智能强力驱动
Strongly Powered by AbleSci AI