4.7 Article

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

期刊

GENES & DEVELOPMENT
卷 32, 期 9-10, 页码 711-722

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.314245.118

关键词

BRF2; SNAPc; TBP; TFIIA; TFIIB; small nuclear RNA promoters

资金

  1. University of Lausanne
  2. Swiss National Foundation [31003A_169233]
  3. Swiss National Science Foundation (SNF) [31003A_169233] Funding Source: Swiss National Science Foundation (SNF)
  4. BBSRC [BB/K014390/1] Funding Source: UKRI

向作者/读者索取更多资源

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.

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