共 108 条
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.
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页码:257 / 265
页数:9
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