Genome-wide location and regulated recruitment of the RSC nucleosome-remodeling complex

  1. Huck Hui Ng1,4,
  2. François Robert2,4,
  3. Richard A. Young2,3, and
  4. Kevin Struhl1,5
  1. 1Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA; 2Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA; 3Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA

Abstract

Genome-wide location analysis indicates that the yeast nucleosome-remodeling complex RSC has ∼700 physiological targets and that the Rsc1 and Rsc2 isoforms of the complex behave indistinguishably. RSC is associated with numerous tRNA promoters, suggesting that the complex is recruited by the RNA polymerase III transcription machinery. At RNA polymerase II promoters, RSC specifically targets several gene classes, including histones, small nucleolar RNAs, the nitrogen discrimination pathway, nonfermentative carbohydrate metabolism, and mitochondrial function. At the histoneHTA1/HTB1 promoter, RSC recruitment requires the Hir1 and Hir2 corepressors, and it is associated with transcriptional inactivity. In contrast, RSC binds to promoters involved in carbohydrate metabolism in response to transcriptional activation, but prior to association of the Pol II machinery. Therefore, the RSC complex is generally recruited to Pol III promoters and it is specifically recruited to Pol II promoters by transcriptional activators and repressors.

Keywords

Footnotes

  • 4 These authors contributed equally to this work.

  • 5 Corresponding author.

  • E-MAIL kevin{at}hms.harvard.edu; FAX (617) 432-2104.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.978902.

    • Received January 24, 2002.
    • Accepted February 15, 2002.
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