Expression and regulation of steroid 5 alpha-reductase in the urogenital tract of the fetal rat
- PMID: 8584033
- DOI: 10.1210/mend.9.11.8584033
Expression and regulation of steroid 5 alpha-reductase in the urogenital tract of the fetal rat
Abstract
Two androgens, testosterone and dihydrotestosterone, are required for the development of the male urogenital tract in the rat. Testosterone is secreted by the fetal testes and is thought to elicit differentiation of the Wolffian ducts into seminal vesicles, vas deferens, and epididymides. Testosterone is converted into dihydrotestosterone by steroid 5 alpha-reductase in the urogenital tract, and this conversion is necessary for the differentiation of the prostate and external genitalia. Genes encoding two 5 alpha-reductase isozymes, designated type 1 and type 2, have been identified. We examined the expression and regulation of these genes on days 17-21 in the urogenital tracts of male and female fetuses. Expression of the type 1 gene predominated in epithelial cells, whereas type 2 gene expression was limited to mesenchymal cells. Surprisingly, this expression pattern was detected in both testosterone-dependent and dihydrotestosterone-dependent anlagen of the urogenital tract and was the same in both male and female fetuses. Furthermore, transcripts encoding the two isozymes were present in their respective cell types before the overt differentiation of internal genitalia. Androgens stimulated expression of the type 2 gene in the urogenital tracts of both sexes, but did not effect expression of the type 1 gene or the cell type-specific expression patterns of the 5 alpha-reductase genes. In the adult prostate, 5 alpha-reductase gene expression is under feedforward control, in which the product of the enzyme, dihydrotestosterone, stimulates the expression of the gene. However, no evidence for feedforward regulation of either 5 alpha-reductase gene was detected in the fetus.
Similar articles
-
5 alpha-reductase activity in developing urogenital tracts of fetal and neonatal male mice.Endocrinology. 1994 May;134(5):2198-205. doi: 10.1210/endo.134.5.8156922. Endocrinology. 1994. PMID: 8156922
-
Differential regulation of steroid 5alpha-reductase isozymes expression by androgens in the adult rat brain.FASEB J. 2003 Aug;17(11):1428-33. doi: 10.1096/fj.02-1119com. FASEB J. 2003. PMID: 12890696
-
Transient expression of the 5alpha-reductase type 2 isozyme in the rat brain in late fetal and early postnatal life.Endocrinology. 1998 Apr;139(4):2171-8. doi: 10.1210/endo.139.4.5866. Endocrinology. 1998. PMID: 9529007
-
Androgens and male physiology the syndrome of 5alpha-reductase-2 deficiency.Mol Cell Endocrinol. 2002 Dec 30;198(1-2):51-9. doi: 10.1016/s0303-7207(02)00368-4. Mol Cell Endocrinol. 2002. PMID: 12573814 Review.
-
[Differentiation of external genitalia and 5 alpha-reductase].Nihon Rinsho. 2004 Feb;62(2):275-80. Nihon Rinsho. 2004. PMID: 14968532 Review. Japanese.
Cited by
-
Glucocorticoids regulate AKR1D1 activity in human liver in vitro and in vivo.J Endocrinol. 2020 May;245(2):207-218. doi: 10.1530/JOE-19-0473. J Endocrinol. 2020. PMID: 32106090 Free PMC article.
-
Semiquantitative RT-PCR method coupled to capillary electrophoresis to study 5alpha-reductase mRNA isozymes in rat ventral prostate in different androgen status.Mol Cell Biochem. 2003 Aug;250(1-2):125-30. doi: 10.1023/a:1024902419502. Mol Cell Biochem. 2003. PMID: 12962150
-
Genome-wide analysis of androgen receptor binding and transcriptomic analysis in mesenchymal subsets during prostate development.Dis Model Mech. 2019 Jul 25;12(7):dmm039297. doi: 10.1242/dmm.039297. Dis Model Mech. 2019. PMID: 31350272 Free PMC article.
-
5-alpha-reductase and the development of the human prostate.Indian J Urol. 2008 Jul;24(3):309-12. doi: 10.4103/0970-1591.42610. Indian J Urol. 2008. PMID: 19468459 Free PMC article.
-
Pluripotent stem cell differentiation as an emerging model to study human prostate development.Stem Cell Res Ther. 2020 Jul 16;11(1):285. doi: 10.1186/s13287-020-01801-9. Stem Cell Res Ther. 2020. PMID: 32678004 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases