Crystal structure of HIV-1 Tat complexed with human P-TEFb and AFF4

Jianyou Gu, Nigar D. Babayeva, Yoshiaki Suwa, Andrey G. Baranovskiy, David H. Price, Tahir H Tahirov

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Developing anti-viral therapies targeting HIV-1 transcription has been hampered by the limited structural knowledge of the proteins involved. HIV-1 hijacks the cellular machinery that controls RNA polymerase II elongation through an interaction of HIV-1 Tat with the positive transcription elongation factor P-TEFb, which interacts with an AF4 family member (AFF1/2/3/4) in the super elongation complex (SEC). Because inclusion of Tat·P-TEFb into the SEC is critical for HIV transcription, we have determined the crystal structure of the Tat·AFF4·P-TEFb complex containing HIV-1 Tat (residues 1-48), human Cyclin T1 (1-266), human Cdk9 (7-332), and human AFF4 (27-69). Tat binding to AFF4·P-TEFb causes concerted structural changes in AFF4 via a shift of helix H5′ of Cyclin T1 and the α-310 helix of AFF4. The interaction between Tat and AFF4 provides structural constraints that explain tolerated Tat mutations. Analysis of the Tat-binding surface of AFF4 coupled with modeling of all other AF4 family members suggests that AFF1 and AFF4 would be preferred over AFF2 or AFF3 for interaction with Tat·P-TEFb. The structure establishes that the Tat-TAR recognition motif (TRM) in Cyclin T1 interacts with both Tat and AFF4, leading to the exposure of arginine side chains for binding to TAR RNA. Furthermore, modeling of Tat Lys28 acetylation suggests that the acetyl group would be in a favorable position for H-bond formation with Asn257 of TRM, thereby stabilizing the TRM in Cyclin T1, and provides a structural basis for the modulation of TAR RNA binding by acetylation of Tat Lys28.

Original languageEnglish (US)
JournalCell Cycle
Volume13
Issue number11
DOIs
StatePublished - Jun 1 2014

Fingerprint

Positive Transcriptional Elongation Factor B
Cyclin T
HIV-1
Acetylation
RNA
RNA Polymerase II
Arginine
Transcription Factors
HIV
Mutation
Proteins

Keywords

  • AFF4
  • Crystal structure
  • HIV
  • P-TEFb
  • Tat

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

Cite this

Gu, J., Babayeva, N. D., Suwa, Y., Baranovskiy, A. G., Price, D. H., & Tahirov, T. H. (2014). Crystal structure of HIV-1 Tat complexed with human P-TEFb and AFF4. Cell Cycle, 13(11). https://doi.org/10.4161/cc.28756

Crystal structure of HIV-1 Tat complexed with human P-TEFb and AFF4. / Gu, Jianyou; Babayeva, Nigar D.; Suwa, Yoshiaki; Baranovskiy, Andrey G.; Price, David H.; Tahirov, Tahir H.

In: Cell Cycle, Vol. 13, No. 11, 01.06.2014.

Research output: Contribution to journalArticle

Gu, J, Babayeva, ND, Suwa, Y, Baranovskiy, AG, Price, DH & Tahirov, TH 2014, 'Crystal structure of HIV-1 Tat complexed with human P-TEFb and AFF4', Cell Cycle, vol. 13, no. 11. https://doi.org/10.4161/cc.28756
Gu, Jianyou ; Babayeva, Nigar D. ; Suwa, Yoshiaki ; Baranovskiy, Andrey G. ; Price, David H. ; Tahirov, Tahir H. / Crystal structure of HIV-1 Tat complexed with human P-TEFb and AFF4. In: Cell Cycle. 2014 ; Vol. 13, No. 11.
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