Reduced fertility in mice deficient for the POU protein sperm-1

  1. Richard V. Pearse II*,,
  2. Daniel W. Drolet*,,
  3. Kristin A. Kalla*,
  4. Farideh Hooshmand*,
  5. John R. Bermingham, Jr.*, and
  6. Michael G. Rosenfeld*
  1. *Eukaryotic Regulatory Biology Program, Howard Hughes Medical Institute, Cellular and Molecular Medicine, and Graduate Program in Biomedical Sciences, University of California, San Diego, CA 92093-0648

Abstract

Members of the POU-homeodomain gene family encode transcriptional regulatory molecules that play important roles in terminal differentiation of many organ systems. Sperm-1 (Sprm-1) is a POU domain factor that is exclusively expressed in the differentiating male germ cell. We show here that the Sprm-1 protein is expressed in the haploid spermatid and that 129/Sv Sprm-1(−/−) mice are subfertile when compared with wild-type or heterozygous littermates yet exhibit normal testicular morphology and produce normal numbers of mobile spermatozoa. Our data suggest that the Sprm-1 protein plays a discrete regulatory function in the haploid spermatid, which is required for the optimal function, but not the terminal differentiation, of the male germ cell.

Footnotes

  • Present address: Nexstar Pharmaceuticals, 2860 Wilderness Place, Boulder, CO 30301.

  • Michael G. Rosenfeld

  • ABBREVIATION:
    CREM,
    cyclic AMP-responsive element modulator
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