Positive Regulation of Steroidogenic Acute Regulatory Protein Gene Expression through the Interaction between Dlx and GATA-4 for Testicular Steroidogenesis

Author:

Nishida Hisayo1,Miyagawa Shinichi1,Vieux-Rochas Maxence2,Morini Monica3,Ogino Yukiko1,Suzuki Kentaro1,Nakagata Naomi1,Choi Hueng-Sik4,Levi Giovanni2,Yamada Gen1

Affiliation:

1. Center for Animal Resources and Development (H.N., S.M., Y.O., K.S., N.N., G.Y.), Graduate School of Medical and Pharmaceutical Sciences and the Global COE Research Program, Kumamoto University, Kumamoto 860-0811, Japan

2. Centre National de la Recherche Scientifique Unité Mixte de Recherche 5166-MNHN (M.V.-R., G.L.), Evolution des Régulations Endocriniennes, 75231 Paris, Cedex 05, France

3. Istituto Nazionale per la Ricerca sul Cancro (M.M.), 16132 Genova, Italy

4. Hormone Research Center (H.-S.C.), School of Biological Science and Technology, Chonnam National University, Gwangju 500-757, Republic of Korea

Abstract

Split hand/foot malformation (SHFM) is syndromic ectrodactyly often associated with mental retardation and/or craniofacial defects. Several clinical reports previously described urogenital dysplasia such as micropenis, hypospadias, and small testis in SHFM patients. Genetic lesions in the Dlx5 and Dlx6 (Dlx5/6) locus are associated with the human genetic disorder SHFM type 1. Although Dlx5/6 are expressed in the testis, their possible function of Dlx5/6 during testis differentiation has not been described. In this study, we show that Dlx5/6 are expressed in the fetal Leydig cells during testis development. We examined the effect of Dlx5 expression on the promoter activation of the steroidogenic acute regulatory protein (StAR) gene, which is essential for gonadal and adrenal steroidogenesis, in a Leydig cell line. Dlx5 efficiently activates the StAR promoter when GATA-4, another transcription factor essential for testicular steroidogenesis, was coexpressed. The transcriptional activation required the GATA-4-recognition element in the StAR promoter region and Dlx5 can physically interact with GATA-4. Furthermore, we herein show that the double inactivation of Dlx5 and Dlx6 in the mouse leads to decreased testosterone level and abnormal masculinization phenotype. These results suggest that Dlx5 and Dlx6 participate in the control of steroidogenesis during testis development. The findings of this study may open the way to analyze human congenital birth defects.

Publisher

The Endocrine Society

Subject

Endocrinology

Reference58 articles.

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