Mammalian Male and Female Germ Cells Express a Germ Cell-Specific Y-Box Protein, MSY21

  1. Wei Gu3,,4,
  2. Seshadri Tekur4,
  3. Rolland Reinbold5,
  4. John J. Eppig6,
  5. Young-Chul Choi4,
  6. Jenny Z. Zheng4,
  7. Mary T. Murray2,,5 and
  8. Norman B. Hecht2,,4
  1. Department of Biology,4 Tufts University, Medford, Massachusetts 02155
  2. Center for Molecular Medicine and Genetics,5 Wayne State University School of Medicine, Detroit, Michigan 48202
  3. The Jackson Laboratory,6 Bar Harbor, Maine 04609

    Abstract

    Here we report the isolation and characterization of mouse testicular cDNAs encoding the mammalian homologue of the Xenopus germ cell-specific nucleic acid-binding protein FRGY2 (mRNP3+4), hereafter designated MSY2. MSY2 is a member of the Y box multigene family of proteins; it contains the cold shock domain that is highly conserved among all Y box proteins and four basic/aromatic islands that are closely related to the other known germline Y box proteins from Xenopus, FRGY2, and goldfish, GFYP2. Msy2 undergoes alternative splicing to yield alternate N-terminal regions upstream of the cold shock domain. Although MSY2 is a member of a large family of nucleic acid-binding proteins, Southern blotting detects only a limited number of genomic DNA fragments, suggesting that Msy2 is a single copy gene. By Northern blotting and immunoblotting, MSY2 appears to be a germ cell-specific protein in the testis. Analysis of Msy2 mRNA expression in prepubertal and adult mouse testes, and in isolated populations of germ cells, reveals maximal expression in postmeiotic round spermatids, a cell type with abundant amounts of stored messenger ribonucleoproteins. In the ovary, MSY2 is present exclusively in diplotene-stage and mature oocytes. MSY2 is maternally inherited in the one-cell-stage embryo but is not detected in the late two-cell-stage embryo. This loss of MSY2 is coincident with the bulk degradation of maternal mRNAs in the two-cell embryo.

    Footnotes

    • 1 Supported by NIH grant HD 29125 (N.B.H.), NSF grant MCB-9513751 (M.T.M.), and NIH grant CA 62392 (J.J.E.).

    • 2 Correspondence: Norman B. Hecht, Center for Research on Reproduction and Women's Health and Department of Obstetrics and Gynecology, University of Pennsylvania Medical Center, 752 Clinical Research Building/6142, Philadelphia, PA 19104–6142, FAX: 215 573 5408; or Mary T. Murray, Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48202.

    • 3 Present address: Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461

      • Accepted July 10, 1998.
      • Received May 28, 1998.
    « Previous | Next Article »Table of Contents