Key result
The human 3 beta-hydroxysteroid dehydrogenase gene spans ~8 kilobases and maps to chromosome 1.
Why the study?
Characterization of the structural gene encoding human 3 beta-hydroxysteroid dehydrogenase/delta 5----4-isomerase is necessary to understand clinical deficiencies caused by mutations in this gene.
Key points are not available for this paper at this time.
Design
Genomic DNA isolation and sequence analysis study
Supports mutation screening in 3β-HSD deficiency; leaves open clinical translation pending functional validation.
The structural gene encoding human 3 beta-hydroxysteroid dehydrogenase/delta 5----4-isomerase (3 beta HSD) was isolated from a human EMBL3 genomic library. The gene encompasses approximately 8 kilobases of DNA and is comprised of two large introns and three exons encoding amino acid residues 1-48, 49-103, and 104-373, respectively. The exonic sequence is identical to that of the cDNA that we previously isolated and expressed in COS 1 cells. DNA sequence analysis reveals a putative TATA (TATATAA) motif 26 basepairs up-stream of the beginning of exon I, as determined by S1 nuclease protection analysis. However, primer extension analysis using poly(A)+ RNA isolated from both placenta and corpora lutea indicates that the RNA initiates up-stream of the putative TATA motif, and that an additional 53-basepair exon, which is untranslated, is present 5' to the first coding exon. Southern hybridization analysis of genomic DNA using a single exon probe suggests that there may be more than one copy of the gene in the human genome. In addition, we confirm from Southern analysis of genomic DNA isolated from human x hamster somatic cell hybrids that the gene is located on human chromosome 1. These findings will provide a foundation for the characterization of apparent 3 beta HSD clinical deficiencies when these are due to a mutation in the structural gene.
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Lorence et al. (1990) studied this question. The human 3 beta-hydroxysteroid dehydrogenase gene encompasses approximately 8 kilobases, contains multiple exons, and is located on human chromosome 1.
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