Department of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge CB2 1GA, U.K.
Biochem Soc Trans. 2012 Apr;40(2):341-6. doi: 10.1042/BST20120014.
Histone H1 and HMGB1 (high-mobility group protein B1) are the most abundant chromosomal proteins apart from the core histones (on average, one copy per nucleosome and per ten nucleosomes respectively). They are both highly mobile in the cell nucleus, with high on/off rates for binding. In vivo and in vitro evidence shows that both are able to organize chromatin structure, with H1 binding resulting in a more stable structure and HMGB1 binding in a less stable structure. The binding sites for H1 and HMGB1 in chromatin are partially overlapping, and replacement of H1 by HMGB1 through the highly dynamic nature of their binding, possibly facilitated by interaction between them, could result in switching of chromatin states. Binding of HMGB1 to DNA or chromatin is regulated by its long and highly acidic tail, which is also involved in H1 binding. The present article focuses mainly on HMGB1 and its interaction with chromatin and H1, as well as its chaperone role in the binding of certain transcription factors (e.g. p53) to their cognate DNA.
组蛋白 H1 和 HMGB1(高迁移率族蛋白 B1)是除核心组蛋白之外细胞核中含量最丰富的染色体蛋白(平均每个核小体和每十个核小体分别有一个拷贝)。它们在细胞核内都具有很高的流动性,与结合物的结合具有很高的开启和关闭速率。体内和体外的证据表明,两者都能够组织染色质结构,H1 的结合导致更稳定的结构,而 HMGB1 的结合导致不太稳定的结构。H1 和 HMGB1 在染色质上的结合位点部分重叠,通过它们之间的相互作用,HMGB1 通过其结合的高度动态性质取代 H1,可能导致染色质状态的转换。HMGB1 与 DNA 或染色质的结合受其长而高度酸性的尾巴调节,该尾巴也参与 H1 的结合。本文主要关注 HMGB1 及其与染色质和 H1 的相互作用,以及它在某些转录因子(如 p53)与其同源 DNA 结合中的伴侣作用。