Fertility and Sterility
Volume 91, Issue 5, Supplement , Pages 2020-2024, May 2009

Expression and localization of the novel and highly conserved gametocyte-specific factor 1 during oogenesis and spermatogenesis

  • Stephan P. Krotz, M.D.

      Affiliations

    • Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas
    • Division of Reproductive Endocrinology, Women and Infants' Hospital of Rhode Island, Warren Alpert Medical School, Brown University, Providence, Rhode Island
    • Corresponding Author InformationReprint requests: Stephan Krotz, M.D., 101 Dudley Street, Division of Reproductive Endocrinology & Infertility, Providence, RI 02905 (FAX: 401-276-7845).
  • ,
  • Daniel J. Ballow, B.A.

      Affiliations

    • Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas
  • ,
  • Youngsok Choi, Ph.D.

      Affiliations

    • Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas
  • ,
  • Aleksandar Rajkovic, M.D., Ph.D.

      Affiliations

    • Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas

Received 9 April 2008; received in revised form 14 May 2008; accepted 15 May 2008. published online 14 August 2008.

Objective

To determine the onset of gametocyte-specific factor 1 (Gtsf1) expression in embryogenesis and its relation to Nobox; and to determine its localization during gonadal development and gametocyte maturation.

Design

Developmental animal study.

Setting

University reproductive biology laboratory.

Animal(s)

Mice ranging in age from embryonic day 12.5 to 8 weeks.

Intervention(s)

Polymerase chain reaction and quantitative polymerase chain reaction were performed to determine the onset of and relative messenger RNA expression. Western blot was performed to confirm protein expression and antibody specificity. In situ hybridization and immunohistochemistry were used determine localization of expression.

Main Outcome Measure(s)

Gtsf1 messenger RNA expression levels during embryogenesis through adulthood in wild-type mice and in newborn Nobox knockout mice; GTSF1 expression and localization in postnatal mice.

Result(s)

Gtsf1 functions downstream of Nobox and is highly expressed in embryonic male and female gonads, localizing to germ cells throughout development. GTSF1 expression is confined to the cytoplasm in all stages of postnatal oocyte maturation and to prespermatogonia during early postnatal testicular development.

Conclusion(s)

The expression pattern of Gtsf1 and its high conservation suggests that it may play an important role in germ cell development. Further characterization of Gtsf1 may elucidate mechanisms involved in premature ovarian failure.

Key Words: Nobox, premature ovarian failure, folliculogenesis, germ cell, gametes

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 S.P.K. has nothing to disclose. D.J.B. has nothing to disclose. Y.C. has nothing to disclose. A.R. has nothing to disclose.

 Supported by a National Institutes of Health grant (HD44858) and a March of Dimes Basil O'Connor Award (5-FY02-266) (both to A.R.).

 Presented as an oral presentation at the 63rd Annual Meeting of the American Society for Reproductive Medicine, October 13–17, 2007, Washington, DC.

PII: S0015-0282(08)01154-0

doi:10.1016/j.fertnstert.2008.05.042

Fertility and Sterility
Volume 91, Issue 5, Supplement , Pages 2020-2024, May 2009