Affiliation:
1. Department of Biological Sciences, Columbia University, New York, New York 10027
2. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461
Abstract
ABSTRACT
Sub1 is implicated in transcriptional activation, elongation, and mRNA 3′-end formation in budding yeast. To gain more insight into its function, we performed a synthetic genetic array screen with
SUB1
that uncovered genetic interactions with genes involved in the high-osmolarity glycerol (HOG) osmoresponse pathway. We find that Sub1 and the HOG pathway are redundant for survival in moderate osmolarity. Chromatin immunoprecipitation analysis shows that Sub1 is recruited to osmoresponse gene promoters during osmotic shock and is required for full recruitment of TBP, TFIIB, and RNA polymerase II (RNAP II) at a subset of these genes. Furthermore, we detect Sub1 at the promoter of every constitutively transcribed RNAP II and, unexpectedly, at every RNAP III gene tested, but not at the RNAP I-transcribed ribosomal DNA promoter. Significantly, deletion of
SUB1
reduced levels of promoter-associated RNAP II or III at these genes, but not TBP levels. Together these data suggest that, in addition to a general role in polymerase recruitment at constitutive RNAP II and RNAP III genes, during osmotic shock, Sub1 facilitates osmoresponse gene transcription by enhancing preinitiation complex formation.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology