Epigenetic transcriptional repression of cellular genes by a viral SET protein

被引:49
作者
Mujtaba, Shiraz [3 ]
Manzur, Karishma L. [3 ]
Gurnon, James R. [1 ,2 ]
Kang, Ming [1 ,2 ]
Van Etten, James L. [1 ,2 ]
Zhou, Ming-Ming [3 ]
机构
[1] Univ Nebraska, Dept Plant Pathol, Lincoln, NE 68583 USA
[2] Univ Nebraska, Nebraska Ctr Virol, Lincoln, NE 68583 USA
[3] NYU, Mt Sinai Sch Med, Dept Struct & Chem Biol, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ncb1772
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Viruses recruit host proteins to secure viral genome maintenance and replication. However, whether they modify host histones directly to interfere with chromatin-based transcription is unknown. Here we report that Paramecium bursaria chlorella virus 1 (PBCV-1) encodes a functional SET domain histone Lys methyltransferase (HKMTase) termed vSET, which is linked to rapid inhibition of host transcription after viral infection. We show that vSET is packaged in the PBCV-1 virion, and that it contains a nuclear localization signal and probably represses host transcription by methylating histone H3 at Lys 27 (H3K27), a modification known to trigger gene silencing in eukaryotes. We also show that vSET induces cell accumulation at the G2/M phase by recruiting the Polycomb repressive complex CBX8 to the methylated H3K27 site in a heterologous system. vSET-like proteins that have H3K27 methylation activity are conserved in chlorella viruses. Our findings suggest a viral mechanism to repress gene transcription by direct modification of chromatin by PBCV-1 vSET.
引用
收藏
页码:1114 / 1122
页数:9
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