Molecular cloning of cDNA for rat ovarian 20α-hydroxysteroid dehydrogenase (HSD1)

R. Miura, K. Shiota*, K. Noda, S. Yagi, T. Ogawa, M. Takahashi


研究成果: Article査読

56 被引用数 (Scopus)


20α-Hydroxysteroid dehydrogenase (20α-HSD, EC catalyses the conversion of progesterone into 20α-dihydroprogesterone (20α-OHP). Previously, we purified the enzyme (37 kDa) from rat ovary and determined its N-terminal amino acid sequence. In the present study we succeeded in cloning a full-length 20α-HSD cDNA. mRNA was extracted from immature rat ovaries after successive treatment with equine chorionic gonadotropin (eCG) and human chorionic gonadotropin (hCG). A cDNA library was constructed in λZAP. For screening, a 576 bp probe was amplified by the PCR using mixed primers based on the N-terminal sequence of 20α-HSD, and labelled with [32P]dCTP. Eight positive clones were isolated from 1.2 x 104 recombinants. Analysis of the nucleotide sequence revealed that one clone of 1.2 kbp cDNA (pHSD12-07) contained a poly-adenylation site and an open reading frame encoding 323 amino acids with the N-terminal sequence of 20α-HSD. The fusion protein of pHSD12-07 produced by Escherichia coli reacted with a specific polyclonal antibody generated against rat ovarian 20α-HSD. In addition, the in vitro transcription-translation product produced by Xenopus oocytes showed 20α-HSD activity and Northern-blotting analysis revealed that the ovaries from normal adult rats contained a 1.2 kb mRNA. Thus we succeeded in isolating a clone encoding the full length of rat ovarian 20α-HSD. The sequence showed high similarity with those of rat liver 3α-hydroxysteroid dehydrogenase (3α-HSD), bovine lung prostaglandin F synthase (PGFS), human liver chlordecone reductase (CDR), frog lens p-crystallin and aldose reductases, indicating that 20α-HSD belongs to the aldo-keto reductase family.

ジャーナルBiochemical Journal
出版ステータスPublished - 1994

ASJC Scopus subject areas

  • 生化学


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