Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

被引:354
作者
Flück, CE
Tajima, T
Pandey, AV
Arlt, W
Okuhara, K
Verge, CF
Jabs, EW
Mendonça, BB
Fujieda, K
Miller, WL [1 ]
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] Hokkaido Univ, Dept Pediat, Sapporo, Hokkaido, Japan
[3] Sydney Childrens Hosp, Dept Endocrinol, Randwick, NSW, Australia
[4] Johns Hopkins Univ, Dept Pediat, Baltimore, MD 21218 USA
[5] Univ Sao Paulo, Hosp Clin, Dept Med, Sao Paulo, Brazil
[6] Asahikawa Med Coll, Dept Pediat, Asahikawa, Hokkaido 078, Japan
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ng1300
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Deficient activities of multiple steroidogenic enzymes have been reported without and with Antley-Bixler syndrome (ABS), but mutations of corresponding cytochrome P450 enzymes have not been found. We identified mutations in POR, encoding P450 oxidoreductase, the obligate electron donor for these enzymes, in a woman with amenorrhea and three children with ABS, even though knock-out of POR is embryonically lethal in mice. Mutations of POR also affect drug-metabolizing P450 enzymes, explaining the association of ABS with maternal fluconazole ingestion.
引用
收藏
页码:228 / 230
页数:3
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