Summary information and primary citation
- PDB-id
-
6mcf;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- transcription
- Method
- NMR
- Summary
- Solution structure of 7sk stem-loop 1 with hiv-1 tat
RNA binding domain
- Reference
-
Pham VV, Salguero C, Khan SN, Meagher JL, Brown WC,
Humbert N, de Rocquigny H, Smith JL, D'Souza VM (2018):
"HIV-1 Tat
interactions with cellular 7SK and viral TAR RNAs
identifies dual structural mimicry." Nat
Commun, 9, 4266. doi: 10.1038/s41467-018-06591-6.
- Abstract
- The HIV Tat protein competes with the 7SK:HEXIM
interaction to hijack pTEFb from 7SK snRNP and recruit it
to the TAR motif on stalled viral transcripts. Here we
solve structures of 7SK stemloop-1 and TAR in complex with
Tat's RNA binding domain (RBD) to gain insights into this
process. We find that 7SK is peppered with arginine
sandwich motifs (ASM)-three classical and one with a pseudo
configuration. Despite having similar RBDs, the presence of
an additional arginine, R52, confers Tat the ability to
remodel the pseudo configuration, required for HEXIM
binding, into a classical sandwich, thus displacing HEXIM.
Tat also uses R52 to remodel the TAR bulge into an ASM
whose structure is identical to that of the remodeled ASM
in 7SK. Together, our structures reveal a dual structural
mimicry wherein viral Tat and TAR have co-opted structural
motifs present in cellular HEXIM and 7SK for productive
transcription of its genome.