Screening for Mutations in the Steroidogenic Acute Regulatory Protein and Steroidogenic Factor-1 Genes, and in CYP11A and Dosage-Sensitive Sex Reversal-Adrenal Hypoplasia Gene on the X Chromosome, Gene-1 (DAX-1), in Hyperandrogenic Hirsute Women1
Abstract Abnormalities in adrenal and/or ovarian steroidogenesis are found in most patients with hirsutism. The rate-limiting step in the synthesis of steroids in the ovary and the adrenal is the conversion of cholesterol into pregnenolone by cholesterol side-chain cleavage enzyme (P450scc), encoded...
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Veröffentlicht in: | The journal of clinical endocrinology and metabolism 2001-04, Vol.86 (4), p.1746-1749 |
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Sprache: | eng |
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Zusammenfassung: | Abstract
Abnormalities in adrenal and/or ovarian steroidogenesis are found in
most patients with hirsutism. The rate-limiting step in the synthesis
of steroids in the ovary and the adrenal is the conversion of
cholesterol into pregnenolone by cholesterol side-chain cleavage enzyme
(P450scc), encoded by the gene CYP11A, after cholesterol
is introduced into the mitochondria by the steroidogenic acute
regulatory protein (StAR). DAX-1 is a repressor of StAR gene
expression, and steroidogenic factor-1 (SF-1) is a regulator of
CYP11A, DAX-1, and StAR gene. Mutations in any of these
factors resulting in gain of function, or loss of repression, of StAR
or P450scc might contribute to the steroidogenic abnormalities present
in hirsute patients.
In the present study we have screened, using heteroduplex analysis, the
genes encoding StAR and SF-1 as well as DAX-1 and CYP11A
for mutations in genomic DNA from 19 women presenting with hirsutism
and increased serum androgen levels. When variants were found, analysis
was extended to a larger group of hyperandrogenic patients and
nonaffected women. Two variants were identified in the SF-1 gene. A
G→C change in exon 6, resulting in an Arg365Pro mutation,
was found in 1 of 45 patients, but not in controls. Also, a
Gly146Ala missense mutation, resulting from a G→C change
in exon 4, was found in 2 of 48 patients and in 2 of 50 nonaffected
individuals. We identified a C→T base pair change at position −33 of
the StAR gene. Three of 48 patients and 3 of 43 controls presented this
variant. No mutations were found in coding regions of the StAR gene.
Analysis of CYP11A-coding regions identified a G→A
change in exon 3, resulting in a Val179Ile missense
mutation. This mutation was found in 1 of 29 patients studied and was
not present in 50 controls. Finally, analysis of DAX-1 showed no
variant in any of the women studied.
In conclusion, mutations in StAR, SF-1, CYP11A, and
DAX-1 are seldom found in hirsute patients and do not explain the
steroidogenic abnormalities found in these women. |
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ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.86.4.7424 |