Mechanism of selective recruitment of RNA polymerases II and III to snRNA gene promoters.

View/ Open
Date
2018-05-01ICR Author
Author
Dergai, O
Cousin, P
Gouge, J
Satia, K
Praz, V
Kuhlman, T
Lhôte, P
Vannini, A
Hernandez, N
Type
Journal Article
Metadata
Show full item recordAbstract
RNA polymerase II (Pol II) small nuclear RNA (snRNA) promoters and type 3 Pol III promoters have highly similar structures; both contain an interchangeable enhancer and "proximal sequence element" (PSE), which recruits the SNAP complex (SNAPc). The main distinguishing feature is the presence, in the type 3 promoters only, of a TATA box, which determines Pol III specificity. To understand the mechanism by which the absence or presence of a TATA box results in specific Pol recruitment, we examined how SNAPc and general transcription factors required for Pol II or Pol III transcription of SNAPc-dependent genes (i.e., TATA-box-binding protein [TBP], TFIIB, and TFIIA for Pol II transcription and TBP and BRF2 for Pol III transcription) assemble to ensure specific Pol recruitment. TFIIB and BRF2 could each, in a mutually exclusive fashion, be recruited to SNAPc. In contrast, TBP-TFIIB and TBP-BRF2 complexes were not recruited unless a TATA box was present, which allowed selective and efficient recruitment of the TBP-BRF2 complex. Thus, TBP both prevented BRF2 recruitment to Pol II promoters and enhanced BRF2 recruitment to Pol III promoters. On Pol II promoters, TBP recruitment was separate from TFIIB recruitment and enhanced by TFIIA. Our results provide a model for specific Pol recruitment at SNAPc-dependent promoters.
Collections
Subject
Humans
RNA Polymerase II
RNA Polymerase III
TATA-Box Binding Protein
Transcription Factor TFIIB
Transcription Factors
RNA, Small Nuclear
TATA Box
Protein Binding
Protein Transport
Mutation
Promoter Regions, Genetic
HEK293 Cells
Protein Domains
Research team
Vannini Group
Language
eng
Date accepted
2018-04-17
License start date
2018-05-21
Citation
Genes & development, 2018, 32 (9-10), pp. 711 - 722
Publisher
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT