PMID- 1425412 OWN - NLM STAT- MEDLINE DCOM- 19921201 LR - 20061115 IS - 0013-7227 (Print) IS - 0013-7227 (Linking) VI - 131 IP - 5 DP - 1992 Nov TI - Cloning of an ovine 11 beta-hydroxysteroid dehydrogenase complementary deoxyribonucleic acid: tissue and temporal distribution of its messenger ribonucleic acid during fetal and neonatal development. PG - 2120-6 AB - Glucocorticoids promote the development of many organ systems vital for extrauterine survival, and fetal cortisol provides the trigger for birth in sheep. The activity of glucocorticoids may be influenced at a cellular level by 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD), which is responsible for the interconversion of cortisol and cortisone. To examine 11 beta-HSD gene expression during fetal development, two overlapping clones which yield a 1.4 kilobase (kb) complementary DNA encoding sheep 11 beta-HSD from a liver library were isolated by using a rat 11 beta-HSD cDNA as the probe. This cDNA contains a 879 base pair open reading frame for a protein of 292 amino acids that has more than 70% sequence identity to rat and human 11 beta-HSDs. To define the tissue distribution of 11 beta-HSD messenger RNA in sheep, selected tissues were collected from one fetus at day 130 and term (approximately 145 days), and from a nonpregnant ewe. Cellular RNA was extracted and subjected to Northern blot analysis, and a single 1.8 kb transcript was detected in the fetal and adult liver, lung, hypothalamus, anterior pituitary, and placenta. This was undetectable in adrenals and kidneys, but a smaller (1.5 kb) transcript was present in fetal and adult kidney RNA. The relative abundance of 11 beta-HSD mRNA was greatest in fetal and adult livers, and it was much higher in adult liver, lung, and kidney than in the corresponding fetal tissues. To examine whether 11 beta-HSD gene expression is developmentally regulated in the fetal sheep, liver, lung, and kidney tissues were taken from fetuses at day 60-70, day 100-110, day 125-130, at term, and from newborn lambs (24-48 h old). In the lung and kidney, the relative abundance of 11 beta-HSD mRNA did not change from day 60 to term but increased in the lungs of newborn lambs. In contrast, 11 beta-HSD mRNA levels in the liver increased between day 125 and term and rose further in the newborn. Collectively, these results demonstrate that 11 beta-HSD gene expression in sheep is regulated in a tissue-specific and developmentally programmed manner. FAU - Yang, K AU - Yang K AD - Lawson Research Institute, St. Joseph's Health Centre, London, Ontario, Canada. FAU - Smith, C L AU - Smith CL FAU - Dales, D AU - Dales D FAU - Hammond, G L AU - Hammond GL FAU - Challis, J R AU - Challis JR LA - eng SI - GENBANK/D13201 SI - GENBANK/D13202 SI - GENBANK/D13203 SI - GENBANK/M94783 SI - GENBANK/M94784 SI - GENBANK/M94785 SI - GENBANK/S46205 SI - GENBANK/X64299 SI - GENBANK/X64300 SI - GENBANK/X69561 PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Endocrinology JT - Endocrinology JID - 0375040 RN - 0 (RNA, Messenger) RN - 9007-49-2 (DNA) RN - EC 1.1.- (Hydroxysteroid Dehydrogenases) RN - EC 1.1.1.146 (11-beta-Hydroxysteroid Dehydrogenases) SB - IM GS - 11&bgr;-HSD MH - 11-beta-Hydroxysteroid Dehydrogenases MH - Adrenal Glands/chemistry/embryology/enzymology MH - Animals MH - Animals, Newborn/*genetics MH - Base Sequence MH - Blotting, Northern MH - Cloning, Molecular MH - DNA/analysis/*genetics MH - Embryonic and Fetal Development/*genetics MH - Female MH - Fetus/chemistry MH - Gene Expression MH - Hydroxysteroid Dehydrogenases/*genetics MH - Hypothalamus/chemistry/embryology/enzymology MH - Liver/*chemistry/embryology/enzymology MH - Lung/chemistry/embryology/enzymology MH - Molecular Sequence Data MH - Pituitary Gland, Anterior/chemistry/embryology/enzymology MH - Placenta/chemistry/embryology/enzymology MH - Pregnancy MH - RNA, Messenger/*analysis/genetics MH - Sheep MH - Tissue Distribution EDAT- 1992/11/01 00:00 MHDA- 1992/11/01 00:01 CRDT- 1992/11/01 00:00 PHST- 1992/11/01 00:00 [pubmed] PHST- 1992/11/01 00:01 [medline] PHST- 1992/11/01 00:00 [entrez] AID - 10.1210/endo.131.5.1425412 [doi] PST - ppublish SO - Endocrinology. 1992 Nov;131(5):2120-6. doi: 10.1210/endo.131.5.1425412.