A molecular link between gene-specific and chromosome-wide transcriptional repression

  1. Diana S. Chu,
  2. Heather E. Dawes1,
  3. Jason D. Lieb2,
  4. Raymond C. Chan,
  5. Annie F. Kuo, and
  6. Barbara J. Meyer3
  1. Howard Hughes Medical Institute and Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, California 94720-3204, USA

Abstract

Gene-specific and chromosome-wide mechanisms of transcriptional regulation control development in multicellular organisms. SDC-2, the determinant of hermaphrodite fate in Caenorhabditis elegans, is a paradigm for both modes of regulation. SDC-2 represses transcription of X chromosomes to achieve dosage compensation, and it also represses the male sex-determination gene her-1 to elicit hermaphrodite differentiation. We show here that SDC-2 recruits the entire dosage compensation complex to her-1, directing thisX-chromosome repression machinery to silence an individual, autosomal gene. Functional dissection of her-1 in vivo revealed DNA recognition elements required for SDC-2 binding, recruitment of the dosage compensation complex, and transcriptional repression. Elements within her-1 differed in location, sequence, and strength of repression, implying that the dosage compensation complex may regulate transcription along the X chromosome using diverse recognition elements that play distinct roles in repression.

Keywords

Footnotes

  • Present addresses: 1Current Biology at Cell Press, 1100 Massachusetts Avenue, Cambridge, MA 02138, USA; 2Howard Hughes Medical Institute and Department of Biochemistry, Stanford University Medical Center, Stanford, CA 94305-5428, USA.

  • 3 Corresponding author.

  • E-MAIL bjmeyer{at}uclink4.berkeley.edu; FAX (510) 643-5584.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.972702.

    • Received December 27, 2001.
    • Accepted February 8, 2002.
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