4.5 Article

Functions of Saccharomyces cerevisiae TFIIF during transcription start site utilization

期刊

MOLECULAR AND CELLULAR BIOLOGY
卷 28, 期 11, 页码 3757-3766

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AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.02272-07

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  1. NIGMS NIH HHS [R29 GM051124, GM51124, R01 GM051124] Funding Source: Medline

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Previous studies have shown that substitutions in the Tfg1 or Tfg2 subunits of Saccharomyces cerevisiae transcription factor IIF (TFIIF) can cause upstream shifts in start site utilization, resulting in initiation patterns that more closely resemble those of higher eukaryotes. In this study, we report the results from multiple biochemical assays analyzing the activities of wild-type yeast TFIIF and the TFIIF Tfg1 mutant containing the E346A substitution (Tfg1-E346A). We demonstrate that TFIIF stimulates formation of the first two phosphodiester bonds and dramatically stabilizes a short RNA-DNA hybrid in the RNA polymerase 11 (RNAPII) active center and, importantly, that the Tfg1-E346A substitution coordinately enhances early bond formation and the processivity of early elongation in vitro. These results are discussed within a proposed model for the role of yeast TFIIF in modulating conformational changes in the RNAPII active center during initiation and early elongation.

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