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PMID: 1840601 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cloning and sequencing of the cDNA for rat liver 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase.

The Journal of biological chemistry ·Vol. 266 ·No. 14 ·1991-05-15 ·Pages 8820-5

Pawlowski JE, Huizinga M, Penning TM

Abstract

Rat liver 3 alpha-hydroxysteroid dehydrogenase (3 alpha-HSD, EC 1.1.1.50) is an NAD(P)(+)-dependent oxidoreductase which will terminate androgen action by converting 5 alpha-dihydrotestosterone to 3 alpha-androstanediol. It is identical to dihydrodiol dehydrogenase and it can function as a 9-, 11-, and 15-hydroxyprostaglandin dehydrogenase. Its reactions are potently inhibited by the nonsteroidal anti-inflammatory drugs (NSAIDs). A cDNA (2.1 kilobases) for 3 alpha-HSD was cloned from a rat liver cDNA expression library in lambda gt11. Portions of the cDNA insert which contained an internal EcoRI site were subcloned into pGEM3, and dideoxysequencing revealed that the cDNA contains an open reading frame of 966 nucleotides which encode a protein of 322 amino acids with a monomer Mr of 37,029. The identity of this clone was confirmed by locating two tryptic peptides and two endoproteinase Lys-C peptides from purified 3 alpha-HSD within the nucleotide sequence. The amino acid sequence of rat liver 3 alpha-HSD bears no significant homology with 3 beta-, 17 beta- or 11 beta-hydroxysteroid dehydrogenases but has striking homology with bovine lung prostaglandin F synthase (69% homology at the amino acid level and 74% homology at the nucleotide level) which is a member of the aldehyde/aldose reductase family. This sequence homology supports previous correlates which suggest that in rat 3 alpha-HSD may represent an important target for NSAIDs. The nucleotide sequence also contains three peptides that have been identified by affinity labeling with either 3 alpha-bromoacetoxyandrosterone (substrate analog) or 11 alpha-bromoacetoxyprogesterone (glucocorticoid analog) to comprise the active site (see accompanying article (Penning, T. M., Abrams, W. R., and Pawlowski, J. E. (1991) J. Biol. Chem. 266, 8826-8834]. The sequence data presented suggests that 3 alpha-HSD, prostaglandin F synthase, and aldehyde/aldose reductases are members of a common gene family.

MeSH Terms
3-Hydroxysteroid Dehydrogenases/genetics Aldehyde Reductase/genetics Amino Acid Sequence Animals Base Sequence Blotting, Northern Cloning, Molecular Crystallins/genetics DNA/genetics Gene Expression Hydroxyprostaglandin Dehydrogenases/genetics Liver/enzymology Molecular Sequence Data Peptide Mapping Peptides/chemistry RNA, Messenger/genetics Rats Rats, Inbred Strains Restriction Mapping
Chemicals
Crystallins Peptides RNA, Messenger DNA 3-Hydroxysteroid Dehydrogenases Hydroxyprostaglandin Dehydrogenases prostaglandin-F synthase Aldehyde Reductase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pawlowski J E
Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia 19104-6084.
Huizinga M
Penning T M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1991-05-15
Pages
8820-5
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA01335 · United States
NCI NIH HHS · CA39504 · United States
NIGMS NIH HHS · GM33464 · United States
Databases
GENBANK
M57622, M57623, M57624, M60203, M60204, M60205, M60206, M61937, M62780, M63262
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