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Biology of Reproduction, Vol 22, 9-17, Copyright © 1980 by Society for the Study of Reproduction
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 5 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.
-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.
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