Sexual dimorphism in diverse metazoans is regulated by a novel class of intertwined zinc fingers

  1. Lingyang Zhu1,4,
  2. Jill Wilken2,
  3. Nelson B. Phillips3,
  4. Umadevi Narendra3,
  5. Ging Chan1,
  6. Stephen M. Stratton2,
  7. Stephen B. Kent2, and
  8. Michael A. Weiss1,3,4,5
  1. 1Center for Molecular Oncology, Departments of Biochemistry & Molecular Biology and Chemistry, The University of Chicago, Chicago, Illinois 60637-5419 USA; 2Gryphon Sciences, South San Francisco, California 94080 USA; 3Department of Biochemistry, Case Western Reserve School of Medicine, Cleveland, Ohio 44106-4935 USA

Abstract

Sex determination is regulated by diverse pathways. Although upstream signals vary, a cysteine-rich DNA-binding domain (the DM motif) is conserved within downstream transcription factors ofDrosophila melanogaster (Doublesex) and Caenorhabditis elegans (MAB-3). Vertebrate DM genes have likewise been identified and, remarkably, are associated with human sex reversal (46, XY gonadal dysgenesis). Here we demonstrate that the structure of the Doublesex domain contains a novel zinc module and disordered tail. The module consists of intertwined CCHC and HCCC Zn2+-binding sites; the tail functions as a nascent recognition α-helix. Mutations in either Zn2+-binding site or tail can lead to an intersex phenotype. The motif binds in the DNA minor groove without sharp DNA bending. These molecular features, unusual among zinc fingers and zinc modules, underlie the organization of a Drosophila enhancer that integrates sex- and tissue-specific signals. The structure provides a foundation for analysis of DM mutations affecting sexual dimorphism and courtship behavior.

Keywords

Footnotes

  • 4 Present address: Division of Immunology, Beckman Research Institute of the City of Hope National Medical Center, Duarte, CA, 91010 USA.

  • 5 Corresponding author.

  • E-MAIL weiss{at}biochemistry.cwru.edu; FAX (216) 368-3419.

    • Received April 14, 2000.
    • Accepted May 22, 2000.
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