Control of α-herpesvirus IE gene expression by HCF-1 coupled chromatin modification activities

被引:64
作者
Kristie, Thomas M. [1 ]
Liang, Yu [1 ]
Vogel, Jodi L. [1 ]
机构
[1] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2010年 / 1799卷 / 3-4期
基金
美国国家卫生研究院;
关键词
HCF-1; Herpesvirus; Coactivator; Set1; LSD1; SIMPLEX-VIRUS TYPE-1; HOST-CELL FACTOR; LATENCY-ASSOCIATED TRANSCRIPT; HISTONE ACETYLTRANSFERASE COMPLEX; DNA-BINDING STRUCTURE; IMMEDIATE-EARLY GENES; COACTIVATOR HCF-1; LYTIC INFECTION; HOMEO DOMAIN; METHYLTRANSFERASE COMPLEX;
D O I
10.1016/j.bbagrm.2009.08.003
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
The immediate early genes of the alpha-herpesviruses HSV and VZV are transcriptionally regulated by viral and cellular factors in a complex combinatorial manner. Despite this complexity and the apparent redundancy of activators, the expression of the viral IE genes is critically dependent upon the cellular transcriptional coactivator HCF-1. Although the role of HCF-1 had remained elusive, recent studies have demonstrated that the protein is a component of multiple chromatin modification complexes including the Set1/MLL1 histone H3K4 methyltransferases. Studies using model viral promoter-reporter systems as well as analyses of components recruited to the viral genome during the initiation of infection have elucidated the significance of HCF-1 chromatin modification complexes in contributing to the final state of modified histones assembled on the viral IE promoters. Strikingly, the absence of HCF-1 results in the accumulation of nucleosomes bearing repressive marks on the viral IE promoters and silencing of viral gene expression. Published by Elsevier B.V.
引用
收藏
页码:257 / 265
页数:9
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