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通过Dlx与GATA-4之间的相互作用对类固醇生成急性调节蛋白基因表达进行正向调控以促进睾丸类固醇生成。

Positive regulation of steroidogenic acute regulatory protein gene expression through the interaction between Dlx and GATA-4 for testicular steroidogenesis.

作者信息

Nishida Hisayo, Miyagawa Shinichi, Vieux-Rochas Maxence, Morini Monica, Ogino Yukiko, Suzuki Kentaro, Nakagata Naomi, Choi Hueng-Sik, Levi Giovanni, Yamada Gen

机构信息

Center for Animal Resources and Development, Graduate School of Medical and Pharmaceutical Sciences and the Global COE Research Program, Kumamoto University, Kumamoto 860-0811, Japan.

出版信息

Endocrinology. 2008 May;149(5):2090-7. doi: 10.1210/en.2007-1265. Epub 2008 Feb 14.

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.

摘要

手足裂畸形(SHFM)是一种常伴有智力发育迟缓及/或颅面缺陷的综合征性缺指(趾)畸形。此前有多项临床报告描述了SHFM患者存在泌尿生殖系统发育异常,如小阴茎、尿道下裂和小睾丸等。Dlx5和Dlx6(Dlx5/6)基因座的遗传损伤与人类1型SHFM遗传病相关。尽管Dlx5/6在睾丸中表达,但其在睾丸分化过程中的可能功能尚未见报道。在本研究中,我们发现Dlx5/6在睾丸发育过程中的胎儿睾丸间质细胞中表达。我们在一种睾丸间质细胞系中检测了Dlx5表达对类固醇生成急性调节蛋白(StAR)基因启动子激活的影响,StAR基因对性腺和肾上腺类固醇生成至关重要。当与另一种对睾丸类固醇生成必不可少的转录因子GATA-4共表达时,Dlx5能有效激活StAR启动子。转录激活需要StAR启动子区域中的GATA-4识别元件,且Dlx5能与GATA-4发生物理相互作用。此外,我们在此表明,小鼠中Dlx5和Dlx6的双基因失活会导致睾酮水平降低和雄性化表型异常。这些结果表明,Dlx5和Dlx6参与睾丸发育过程中类固醇生成的调控。本研究结果可能为分析人类先天性出生缺陷开辟道路。

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