The 7SK small nuclear RNA inhibits the CDK9/cyclin T1 kinase to control transcription

Zhiyuan Yang, Qingwei Zhu, Kunxin Luo and Qiang Zhou
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Zhiyuan Yang: University of California at Berkeley
Qingwei Zhu: University of California at Berkeley
Kunxin Luo: University of California at Berkeley
Qiang Zhou: University of California at Berkeley

Nature, 2001, vol. 414, issue 6861, 317-322

Abstract: Abstract The human positive transcription elongation factor P-TEFb, consisting of a CDK9/cyclin T1 heterodimer, functions as both a general and an HIV-1 Tat-specific transcription factor1,2. P-TEFb activates transcription by phosphorylating RNA polymerase (Pol) II, leading to the formation of processive elongation complexes. As a Tat cofactor, P-TEFb stimulates HIV-1 transcription by interacting with Tat and the transactivating responsive (TAR) RNA structure located at the 5′ end of the nascent viral transcript3. Here we identified 7SK, an abundant and evolutionarily conserved small nuclear RNA (snRNA) of unknown function4,5, as a specific P-TEFb-associated factor. 7SK inhibits general and HIV-1 Tat-specific transcriptional activities of P-TEFb in vivo and in vitro by inhibiting the kinase activity of CDK9 and preventing recruitment of P-TEFb to the HIV-1 promoter. 7SK is efficiently dissociated from P-TEFb by treatment of cells with ultraviolet irradiation and actinomycin D. As these two agents have been shown to significantly enhance HIV-1 transcription and phosphorylation of Pol II (refs 6,7,8), our data provide a mechanistic explanation for their stimulatory effects. The 7SK/P-TEFb interaction may serve as a principal control point for the induction of cellular and HIV-1 viral gene expression during stress-related responses. Our studies demonstrate the involvement of an snRNA in controlling the activity of a Cdk–cyclin kinase.

Date: 2001
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DOI: 10.1038/35104575

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