HIV-1 transcription is regulated by splicing factor SRSF1

被引:39
作者
Paz, Sean [1 ]
Krainer, Adrian R. [2 ]
Caputi, Massimo [1 ]
机构
[1] Florida Atlantic Univ, Charles E Schmidt Coll Med, Boca Raton, FL 33431 USA
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
关键词
RNA-POLYMERASE-II; SR PROTEINS; P-TEFB; RECOGNITION MOTIFS; TAT; ELONGATION; BINDING; COMPLEX; HEXIM1; 7SK;
D O I
10.1093/nar/gku1170
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
Efficient transcription of the HIV-1 genome is regulated by Tat, which recruits P-TEFb from the 7SK small nuclear ribonucleoprotein (snRNP) and other nucleoplasmic complexes to phosphorylate RNA polymerase II and other factors associated with the transcription complex. Although Tat activity is dependent on its binding to the viral TAR sequence, little is known about the cellular factors that might also assemble onto this region of the viral transcript. Here, we report that the splicing factor SRSF1 (SF2/ASF) and Tat recognize overlapping sequences within TAR and the 7SK RNA. SRSF1 expression can inhibit Tat transactivation by directly competing for its binding to TAR. Additionally, we provide evidence that SRSF1 can increase the basal level of viral transcription in the absence of Tat. We propose that SRSF1 activates transcription in the early stages of viral infection by recruiting P-TEFb to TAR from the 7SK snRNP. Whereas in the later stages, Tat substitutes for SRSF1 by promoting release of the stalled polymerase and more efficient transcriptional elongation.
引用
收藏
页码:13812 / 13823
页数:12
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