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Linking cell cycle to histone modifications: SBF and H2B monoubiquitination machinery and cell-cycle regulation of H3K79 dimethylation.
Schulze, Julia M; Jackson, Jessica; Nakanishi, Shima; Gardner, Jennifer M; Hentrich, Thomas; Haug, Jeff; Johnston, Mark; Jaspersen, Sue L; Kobor, Michael S; Shilatifard, Ali.
Afiliação
  • Schulze JM; Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC, Canada.
Mol Cell ; 35(5): 626-41, 2009 Sep 11.
Article em En | MEDLINE | ID: mdl-19682934
ABSTRACT
To identify regulators involved in determining the differential pattern of H3K79 methylation by Dot1, we screened the entire yeast gene deletion collection by GPS for genes required for normal levels of H3K79 di- but not trimethylation. We identified the cell cycle-regulated SBF protein complex required for H3K79 dimethylation. We also found that H3K79 di- and trimethylation are mutually exclusive, with M/G1 cell cycle-regulated genes significantly enriched for H3K79 dimethylation. Since H3K79 trimethylation requires prior monoubiquitination of H2B, we performed genome-wide profiling of H2BK123 monoubiquitination and showed that H2BK123 monoubiquitination is not detected on cell cycle-regulated genes and sites containing H3K79me2, but is found on H3K79me3-containing regions. A screen for genes responsible for the establishment/removal of H3K79 dimethylation resulted in identification of NRM1 and WHI3, both of which impact the transcription by the SBF and MBF protein complexes, further linking the regulation of methylation status of H3K79 to the cell cycle.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Fatores de Transcrição / Proteínas Nucleares / Histonas / Ciclo Celular / Processamento de Proteína Pós-Traducional / Histona-Lisina N-Metiltransferase / Proteínas de Saccharomyces cerevisiae / Enzimas de Conjugação de Ubiquitina Tipo de estudo: Prognostic_studies Idioma: En Revista: Mol Cell Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Fatores de Transcrição / Proteínas Nucleares / Histonas / Ciclo Celular / Processamento de Proteína Pós-Traducional / Histona-Lisina N-Metiltransferase / Proteínas de Saccharomyces cerevisiae / Enzimas de Conjugação de Ubiquitina Tipo de estudo: Prognostic_studies Idioma: En Revista: Mol Cell Ano de publicação: 2009 Tipo de documento: Article