Structure of Two in Tandem Human 17β-Hydroxysteroid Dehydrogenase Genes
Author(s) -
Van LuuThe,
Claude Labrie,
Jacques Simard,
Yves Lachance,
Huifen Zhao,
Jacques Couët,
Gilles Leblanc,
Fernand Labrie
Publication year - 1990
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/mend-4-2-268
Subject(s) - biology , exon , intron , complementary dna , gene , microbiology and biotechnology , genomic dna , genetics , tandem exon duplication , genomic library , cdna library , nucleic acid sequence , hydroxysteroid dehydrogenase , homology (biology) , hydroxysteroid , peptide sequence , dehydrogenase , biochemistry , enzyme
Two human 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD) genes (h17 beta-HSDI and h17 beta-HSDII) included in tandem within an approximately 13 kilobase pair fragment were isolated from a genomic lambda EMBL3 DNA library using cDNA encoding human 17 beta-HSD (hpE2DH216) as probe. We have determined the complete exon and intron sequences of the two genes as well as their 5' and 3'-flanking regions. Human 17 beta-HSDII contains six exons and five short introns for a total length of 3250 base pairs. The exon sequence of h17 beta-HSDII is identical to the previously reported hpE2DH216 cDNA while the overlapping nucleotide sequences of the corresponding exons and introns of h17 beta-HSDI and h17 beta-HSDII show 89% homology. In addition, we have used the hpE2DH216 cDNA to demonstrate the widespread expression of 17 beta-HSD mRNAs in steroidogenic and peripheral target tissues. These new findings provide the basis for a better understanding of the molecular mechanisms involved in 17 beta-HSD deficiency and peripheral sex steroid metabolism.
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