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

被引:88
作者
YANG, K
SMITH, CL
DALES, D
HAMMOND, GL
CHALLIS, JRG
机构
[1] UNIV WESTERN ONTARIO,LONDON REG CANC CTR,LONDON N6A 4V2,ONTARIO,CANADA
[2] UNIV WESTERN ONTARIO,DEPT BIOCHEM,LONDON N6A 4V2,ONTARIO,CANADA
[3] UNIV WESTERN ONTARIO,DEPT ONCOL,LONDON N6A 4V2,ONTARIO,CANADA
[4] UNIV WESTERN ONTARIO,DEPT OBSTET & GYNECOL,MRC,FETAL & NEONATAL HLTH & DEV GRP,LONDON N6A 4V2,ONTARIO,CANADA
[5] UNIV WESTERN ONTARIO,DEPT PHYSIOL,LONDON N6A 4V2,ONTARIO,CANADA
关键词
D O I
10.1210/en.131.5.2120
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 11beta-hydroxysteroid dehydrogenase (11beta-HSD), which is responsible for the interconversion of cortisol and cortisone. To examine 11beta-HSD gene expression during fetal development, two over-lapping clones which yield a 1.4 kilobase (kb) complementary DNA encoding sheep 11beta-HSD from a liver library were isolated by using a rat 11beta-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 11beta-HSDs. To define the tissue distribution of 11beta-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 11beta-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 11beta-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 11beta-HSD mRNA did not change from day 60 to term but increased in the lungs of newborn lambs. In contrast, 11beta-HSD mRNA levels in the liver increased between day 125 and term and rose further in the newborn. Collectively, these results demonstrate that 110-HSD gene expression in sheep is regulated in a tissue-specific and developmentally programmed manner.
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页码:2120 / 2126
页数:7
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