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Genome-wide association of mediator and RNA polymerase II in wild-type and mediator mutant yeast.
Paul, Emily; Zhu, Z Iris; Landsman, David; Morse, Randall H.
Afiliación
  • Paul E; Laboratory of Molecular Genetics, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
  • Zhu ZI; Computational Biology Branch, National Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, Maryland, USA.
  • Landsman D; Computational Biology Branch, National Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, Maryland, USA landsman@ncbi.nlm.nih.gov randall.morse@health.ny.gov.
  • Morse RH; Laboratory of Molecular Genetics, Wadsworth Center, New York State Department of Health, Albany, New York, USA Department of Biomedical Science, University at Albany School of Public Health, Albany, New York, USA landsman@ncbi.nlm.nih.gov randall.morse@health.ny.gov.
Mol Cell Biol ; 35(1): 331-42, 2015 Jan.
Article en En | MEDLINE | ID: mdl-25368384
Mediator is a large, multisubunit complex that is required for essentially all mRNA transcription in eukaryotes. In spite of the importance of Mediator, the range of its targets and how it is recruited to these is not well understood. Previous work showed that in Saccharomyces cerevisiae, Mediator contributes to transcriptional activation by two distinct mechanisms, one depending on the tail module triad and favoring SAGA-regulated genes, and the second occurring independently of the tail module and favoring TFIID-regulated genes. Here, we use chromatin immunoprecipitation sequencing (ChIP-seq) to show that dependence on tail module subunits for Mediator recruitment and polymerase II (Pol II) association occurs preferentially at SAGA-regulated over TFIID-regulated genes on a genome-wide scale. We also show that recruitment of tail module subunits to active gene promoters continues genome-wide when Mediator integrity is compromised in med17 temperature-sensitive (ts) yeast, demonstrating the modular nature of the Mediator complex in vivo. In addition, our data indicate that promoters exhibiting strong and stable occupancy by Mediator have a wide range of activity and are enriched for targets of the Tup1-Cyc8 repressor complex. We also identify a number of strong Mediator occupancy peaks that overlap dubious open reading frames (ORFs) and are likely to include previously unrecognized upstream activator sequences.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / ARN Polimerasa II / Regulación Fúngica de la Expresión Génica / Proteínas de Saccharomyces cerevisiae / Complejo Mediador Tipo de estudio: Risk_factors_studies Idioma: En Revista: Mol Cell Biol Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / ARN Polimerasa II / Regulación Fúngica de la Expresión Génica / Proteínas de Saccharomyces cerevisiae / Complejo Mediador Tipo de estudio: Risk_factors_studies Idioma: En Revista: Mol Cell Biol Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos