HIV-1 TAR RNA enhances the interaction between Tat and cyclin T1

被引:63
作者
Zhang, J
Tamilarasu, N
Hwang, SW
Garber, ME
Huq, I
Jones, KA
Rana, TM
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pharmacol, Piscataway, NJ 08854 USA
[2] Salk Inst Biol Studies, Regulatory Biol Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1074/jbc.M006804200
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
Human immunodeficiency virus, type 1 (HIV-1), Tat activates elongation of RNA polymerase II transcription at the HIV-1 promoter through interaction with the cyclin T1 (CycT1) subunit of the positive transcription elongation factor complex, P-TEFb, Binding of Tat to CycT1 induces cooperative binding of the beta -TEFb complex onto nascent HIV-1 TAR RNA. Here the specific interaction between Tat protein, human cyclin T1, and HIV-1 TAR RNA was analyzed by fluorescence resonance energy transfer, using fluorescein-labeled TAR RNA and a rhodamine-labeled Tat protein synthesized through solid-phase chemistry. We find that CycT1 remodels the structure of Tat to enhance its affinity for TAR RNA and that TAR RNA further enhances the interaction between Tat and CycT1, We conclude that TAR RNA nucleates the formation of the Tat.beta -TEFb complex through an induced fit mechanism.
引用
收藏
页码:34314 / 34319
页数:6
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