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  • 1.
    Wiren, Marianna
    et al.
    Södertörn University, School of Life Sciences. Karolinska Institutet.
    Silverstein, Rebecca A
    Södertörn University, School of Life Sciences. Karolinska Institutet.
    Sinha, Indranil
    Södertörn University, School of Life Sciences. Karolinska Institutet.
    Walfridsson, Julian
    Södertörn University, School of Life Sciences. Karolinska Institutet.
    Lee, Hang-mao
    Södertörn University, School of Life Sciences. Karolinska Institutet.
    Laurenson, P
    University of California, San Diego, USA.
    Pillus, L
    University of California, San Diego, USA.
    Robyr, D
    University of California, Los Angeles, USA.
    Grunstein, M
    University of California, Los Angeles, USA.
    Ekwall, Karl
    Södertörn University, School of Life Sciences. Karolinska Institutet.
    Genomewide analysis of nucleosome density histone acetylation and HDAC function in fission yeast2005In: EMBO Journal, ISSN 0261-4189, E-ISSN 1460-2075, Vol. 24, no 16, p. 2906-2918Article in journal (Refereed)
    Abstract [en]

    We have conducted a genomewide investigation into the enzymatic specificity, expression profiles, and binding locations of four histone deacetylases (HDACs), representing the three different phylogenetic classes in fission yeast ( Schizosaccharomyces pombe). By directly comparing nucleosome density, histone acetylation patterns and HDAC binding in both intergenic and coding regions with gene expression profiles, we found that Sir2 ( class III) and Hos2 ( class I) have a role in preventing histone loss; Clr6 ( class I) is the principal enzyme in promoter-localized repression. Hos2 has an unexpected role in promoting high expression of growth-related genes by deacetylating H4K16Ac in their open reading frames. Clr3 ( class II) acts cooperatively with Sir2 throughout the genome, including the silent regions: rDNA, centromeres, mat2/3 and telomeres. The most significant acetylation sites are H3K14Ac for Clr3 and H3K9Ac for Sir2 at their genomic targets. Clr3 also affects subtelomeric regions which contain clustered stress- and meiosis-induced genes. Thus, this combined genomic approach has uncovered different roles for fission yeast HDACs at the silent regions in repression and activation of gene expression.

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