Human SFMBT is a transcriptional repressor protein that selectively binds the N-terminal tail of histone H3

被引:45
作者
Wu, Shumin
Trievel, Raymond C.
Rice, Judd C.
机构
[1] Univ So Calif, Keck Sch Med, Dept Biochem & Mol Biol, Los Angeles, CA 90033 USA
[2] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
来源
FEBS LETTERS | 2007年 / 581卷 / 17期
关键词
SFMBT; polycomb; transcription; chromatin; histone H3; THYROID-HORMONE RECEPTOR; POLYCOMB GROUP; STRUCTURAL BASIS; SEX-COMB; CELLULAR MEMORY; ZINC-FINGER; DNA-BINDING; MIDLEG SCM; H4; LYS-20; DROSOPHILA;
D O I
10.1016/j.febslet.2007.06.025
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
Human SFMBT (hSFMBT) is postulated to be a Polycomb (PcG) protein. Similar to other PcG proteins, we found that hSFMBT displays robust transcriptional repressor activity. In addition, hSFMBT localized to the nucleus where it strongly associates with chromatin by directly and selectively binding the N-terminal tail of histone H3. Importantly, we discovered that the four tandem MBT repeats of hSFMBT were sufficient for nuclear matrix-association, N-terminal tail H3 binding, and required for transcriptional repression. These findings indicate that the tandem MBT repeats form a functional structure required for biological activity of hSFMBT and predict similar properties for other MBT domain-containing proteins. (C) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3289 / 3296
页数:8
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