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DAX-1的DNA结合与转录抑制作用会阻断类固醇生成。

DNA binding and transcriptional repression by DAX-1 blocks steroidogenesis.

作者信息

Zazopoulos E, Lalli E, Stocco D M, Sassone-Corsi P

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS-INSERM-ULP BP 163, Strasbourg, France.

出版信息

Nature. 1997 Nov 20;390(6657):311-5. doi: 10.1038/36899.

Abstract

Mutations in the DAX-1 gene are responsible for congenital X-linked adrenal hypoplasia, a disease that is associated with hypogonadotropic hypogonadism. DAX-1 expression is tissue-specific and is finely regulated throughout development, suggesting that it has a role in both adrenal and gonadal function. DAX-1 is an unusual member of the nuclear-receptor superfamily of transcription factors which contains no canonical zinc-finger or any other known DNA-binding motif. Binding sites for DAX-1 are found in the promoters of the dax-1 and StAR (for steroidogenic acute regulatory protein) genes. Here we show that DAX-1 binds DNA and acts as a powerful transcriptional repressor of StAR gene expression, leading to a drastic decrease in steroid production. We provide in vitro and in vivo evidence that DAX-1 binds to DNA hairpin structures. Our results establish DAX-1 as the first member of the nuclear receptor superfamily with novel DNA-binding features and reveal that it has regulatory properties critical to the understanding of its physiological functions.

摘要

DAX-1基因的突变会导致先天性X连锁肾上腺发育不全,这种疾病与促性腺激素缺乏性性腺功能减退有关。DAX-1的表达具有组织特异性,并且在整个发育过程中受到精细调控,这表明它在肾上腺和性腺功能中都发挥作用。DAX-1是转录因子核受体超家族中一个不同寻常的成员,它不包含典型的锌指结构或任何其他已知的DNA结合基序。在dax-1和StAR(类固醇生成急性调节蛋白)基因的启动子中发现了DAX-1的结合位点。在这里,我们表明DAX-1结合DNA并作为StAR基因表达的强大转录抑制因子,导致类固醇生成急剧减少。我们提供了体外和体内证据,证明DAX-1与DNA发夹结构结合。我们的结果确立了DAX-1作为核受体超家族中第一个具有新型DNA结合特征的成员,并揭示了它具有对理解其生理功能至关重要的调节特性。

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