Biol Reprod Lalor Postdoctoral Fellowships -- Application Deadline January 15, 2009
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by WILSON, J. D.
Right arrow Articles by GEORGE, F. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by WILSON, J. D.
Right arrow Articles by GEORGE, F. W.
Agricola
Right arrow Articles by WILSON, J. D.
Right arrow Articles by GEORGE, F. W.

Biology of Reproduction, Vol 22, 9-17, Copyright © 1980 by Society for the Study of Reproduction

Sexual Differentiation: Early Hormone Synthesis and Action

JEAN D. WILSON 1, JAMES E. GRIFFIN 1, , and FREDRICK W. GEORGE 1

1 Department of Internal Medicine and The Eugene McDermott Center for Growth and Development, University of Texas Southwestern Medical School, Dallas, Texas 75235


Male and female embryos develop in an identical fashion during the initial phases of gestation and it is only after the gonads differentiate and endocrine function of the testis is initiated that male phenotypic differentiation can occur. If an ovary (or no gonad) is present the final phenotype is female; thus, no gonadal hormones appear to be required for development of the female phenotype. In contrast, two secretions of the fetal testis, Mullerian regression factor and testosterone, are responsible for the formation of the male phenotype. The former, a poorly characterized peptide hormone, is responsible for suppression of the Mullerian ducts. The remainder of male development is due directly or indirectly to testosterone secretion. The onset of testosterone synthesis in the fetal testis takes place just prior to the onset of male phenotypic differentiation and the process appears to be initially independent of gonadotropin control. Studies of single gene mutations that interfere with androgen action have indicated that testosterone itself is responsible for virilization of the Wolffian duct system into the epididymis, vas deferens and seminal vesicles, whereas the testosterone metabolite dihydrotestosterone induces the development of the prostate and male external genitalia. Thus, in 5agr-reductase deficiency, an autosomal recessive disorder in which dihydrotestosterone formation is impaired. virilization of the Wolffian ducts is normal, but the external genitalia and urogenital sinus derivatives are female in character. In the X-linked disorders of the androgen receptor, a high affinity receptor necessary for the translocation of both testosterone and dihydrotestosterone into the nucleus is deficient or abnormal, the actions of both hormones are impaired and developmental abnormalities may involve both Wolffian derivatives and the external genitalia as well.

In summary, the development of gonadal sex dictates the development of phenotypic sex with androgen secretion by the fetal testis serving as the agent for virilization of the Wolffian ducts, urogenital sinus, and the external genitalia. The molecular mechanisms by which the hormones act during fetal development appear to be the same as those operative in the postnatal state.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1980 by the Society for the Study of Reproduction.