The Control of HIV Transcription: Keeping RNA Polymerase II on Track

被引:213
作者
Ott, Melanie [1 ,4 ]
Geyer, Matthias [2 ]
Zhou, Qiang [3 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol, San Francisco, CA 94158 USA
[2] Max Planck Inst Mol Physiol, D-44227 Dortmund, Germany
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[4] Univ Calif San Francisco, Gladstone Inst Immunol, San Francisco, CA 94158 USA
关键词
T-BINDING DOMAIN; P-TEFB; TAT TRANSACTIVATION; ELONGATION COMPLEX; 7SK SNRNA; HISTONE ACETYLTRANSFERASE; ARGININE METHYLATION; CDK9/CYCLIN T1; CYCLIN T1; PROTEIN;
D O I
10.1016/j.chom.2011.11.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Thirteen years ago, human cyclin T1 was identified as part of the positive transcription elongation factor b (P-TEFb) and the long-sought host cofactor for the HIV-1 transactivator Tat. Recent years have brought new insights into the intricate regulation of P-TEFb function and its relationship with Tat, revealing novel mechanisms for controlling HIV transcription and fueling new efforts to overcome the barrier of transcriptional latency in eradicating HIV. Moreover, the improved understanding of HIV and Tat forms a basis for studying transcription elongation control in general. Here, we review advances in HIV transcription research with a focus on the growing family of cellular P-TEFb complexes, structural insights into the interactions between Tat, P-TEFb, and TAR RNA, and the multifaceted regulation of these interactions by posttranscriptional modifications of Tat.
引用
收藏
页码:426 / 435
页数:10
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