PMID- 10103023 OWN - NLM STAT- MEDLINE DCOM- 19990506 LR - 20190620 IS - 0014-2956 (Print) IS - 0014-2956 (Linking) VI - 260 IP - 3 DP - 1999 Mar TI - Expression of 3beta-hydroxysteroid dehydrogenase type I and type VI isoforms in the mouse testis during development. PG - 911-7 AB - Six isoforms of the enzyme 3beta-hydroxysteroid dehydrogenase (3betaHSD) have been identified in the mouse, each the product of a distinct gene. Two of these isoforms (type I and type VI) are detectable in the adult testis but changes in their expression during development are unknown. In this study we have examined changes in testicular expression and localization of mRNA encoding the type I and type VI isoforms of 3betaHSD. Total 3betaHSD (type I plus type VI) mRNA was measured by reverse transcription-polymerase chain reaction and showed a peak of expression at day 5 after birth followed by a decline and then a further rise after day 10 that continued up to adulthood. When each isoform was measured individually it was clear that the type I isoform was expressed at all ages from embryonic day 13 to adulthood. In contrast, the type VI isoform was only expressed at significant levels during fetal life on embryonic day 13 and then not again until after day 10 postnatally. Expression of the type VI isoform mRNA increased markedly after day 10 so that by adulthood it was the predominant 3betaHSD isoform present in the testis. Closer examination of the timing of type VI expression showed that the isoform mRNA was first detectable at a significant level on day 11. In-situ hybridization confirmed that the type I isoform is the only one expressed in the fetal/neonatal animal and showed that expression was limited to the interstitial tissue. In the adult, both type I and type VI expression was within the interstitial tissue. The timing of 3betaHSD type VI mRNA expression suggests, strongly, that this isoform is expressed only by adult-type Leydig cells in the mouse testis and that this development starts shortly before day 11. The limited expression of the type VI isoform means that it will be a useful marker in studies of adult Leydig cell development. FAU - Baker, P J AU - Baker PJ AD - Division of Veterinary Physiology, Department of Veterinary Pre-clinical Studies, University of Glasgow Veterinary School, UK. FAU - Sha, J A AU - Sha JA FAU - McBride, M W AU - McBride MW FAU - Peng, L AU - Peng L FAU - Payne, A H AU - Payne AH FAU - O'Shaughnessy, P J AU - O'Shaughnessy PJ LA - eng GR - U54 HD31398/HD/NICHD NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - England TA - Eur J Biochem JT - European journal of biochemistry JID - 0107600 RN - 0 (Isoenzymes) RN - 0 (RNA, Messenger) RN - EC 1.1.- (3-Hydroxysteroid Dehydrogenases) SB - IM MH - 3-Hydroxysteroid Dehydrogenases/*biosynthesis/genetics MH - Animals MH - Female MH - In Situ Hybridization MH - In Vitro Techniques MH - Isoenzymes/*biosynthesis/genetics MH - Leydig Cells/enzymology MH - Male MH - Mice MH - RNA, Messenger/biosynthesis MH - Testis/cytology/*enzymology/*growth & development EDAT- 1999/04/02 00:00 MHDA- 1999/04/02 00:01 CRDT- 1999/04/02 00:00 PHST- 1999/04/02 00:00 [pubmed] PHST- 1999/04/02 00:01 [medline] PHST- 1999/04/02 00:00 [entrez] AID - 10.1046/j.1432-1327.1999.00245.x [doi] PST - ppublish SO - Eur J Biochem. 1999 Mar;260(3):911-7. doi: 10.1046/j.1432-1327.1999.00245.x.