Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, U.S.A.
Essays Biochem. 2019 Apr 23;63(1):75-87. doi: 10.1042/EBC20180056.
In eukaryotic cells, genomic DNA exists in the form of chromatin through association with histone proteins, which consist of four core histone (H2A, H2B, H3, and H4) families and one linker histone (H1) family. The core histones bind to DNA to form the nucleosome, the recurring structural unit of chromatin. The linker histone binds to the nucleosome to form the next structural unit of chromatin, the chromatosome, which occurs dominantly in metazoans. Linker histones also play an essential role in condensing chromatin to form higher order structures. Unlike the core histones in the formation of the nucleosome, the role of linker histone in the formation of the chromatosome and high-order chromatin structure is not well understood. Nevertheless, exciting progress in the structural studies of chromatosomes and nucleosome arrays condensed by linker histones has been made in the last several years. In this mini-review, we discuss these recent experimental results and provide some perspectives for future studies.
在真核细胞中,基因组 DNA 通过与组蛋白蛋白结合存在于染色质形式中,组蛋白蛋白由四个核心组蛋白(H2A、H2B、H3 和 H4)家族和一个连接组蛋白(H1)家族组成。核心组蛋白与 DNA 结合形成核小体,这是染色质的重复结构单元。连接组蛋白与核小体结合形成染色质的下一个结构单元,即染色质小体,它主要存在于后生动物中。连接组蛋白在将染色质浓缩形成更高阶结构方面也起着至关重要的作用。与核小体形成中的核心组蛋白不同,连接组蛋白在染色质小体和高阶染色质结构形成中的作用尚未得到很好的理解。然而,近年来在连接组蛋白浓缩的染色质小体和核小体阵列的结构研究方面取得了令人兴奋的进展。在这篇综述中,我们讨论了这些最近的实验结果,并为未来的研究提供了一些观点。