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Developmental Endocrinology Unit (R.V.C., S.D., A.E.C.B., B.B.M.), Hospital das Clínicas, Faculdade Medicina Universidade de São Paulo, São Paulo 05403-900, Brazil; and Departments of Internal Medicine and Pharmacology (N.C.B., W.E.R., K.L.P.), University of Texas Southwestern Medical Center, Dallas, Texas 75390-8857
Address all correspondence and requests for reprints to: Dr. Berenice B. Mendonca, Rua Dr Eneas de Carvalho Aguiar 155 PAMB 2 andar Bl. 06, Sao Paulo SP, 05403-900, Brazil. E-mail: beremen{at}usp.br; rafaelac{at}usp.br.
Steroidogenic factor 1 (SF-1) is an orphan nuclear receptor that plays key roles in endocrine development and function. Knockout mice lacking SF-1 have adrenal and gonadal agenesis, impaired gonadotropin expression, and structural abnormalities of the ventromedial hypothalamic nucleus. Previous studies have identified three human subjects with mutations in SF-1 causing adrenocortical insufficiency with varying degrees of gonadal dysfunction. We now describe a novel 8-bp microdeletion of SF-1, isolated from a 46, XY patient who presented with gonadal agenesis but normal adrenal function, which causes premature termination upstream of sequences encoding the activation function 2 domain. In cell transfection experiments, the mutated protein possessed no intrinsic transcriptional activity but rather inhibited the function of the wild-type protein in most cell types. To our knowledge, this is the first example of an apparent dominant-negative effect of a SF-1 mutation in humans. These findings, which define a SF-1 mutation that apparently differentially affects its transcriptional activity in vivo in the adrenal cortex and the gonads, may be relevant to the cohort of patients who present with 46, XY sex reversal but normal adrenal function.
This work was partially supported by grants from Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP 00/06678-9, to R.V.C., 00/01737-7, to S.D.), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq 301246/95-5, to B.B.M.), and the National Institutes of Health Grant DK54480 (to K.L.P.). N.B. was supported by the Pharmacology Training Grant at University of Texas Southwestern.
Abbreviations: AF-2, Activation function 2; HA, hemagglutinin; hCG, human chorionic gonadotropin; SF-1, steroidogenic factor 1; WT, wild-type.
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