首页> 美国卫生研究院文献>The Journal of Biological Chemistry >ARR19 (Androgen Receptor Corepressor of 19 kDa) an Antisteroidogenic Factor Is Regulated by GATA-1 in Testicular Leydig Cells
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ARR19 (Androgen Receptor Corepressor of 19 kDa) an Antisteroidogenic Factor Is Regulated by GATA-1 in Testicular Leydig Cells

机译:抗甾醇生成因子ARR19(19 kDa的雄激素受体共加压子)受睾丸间质细胞中GATA-1的调控。

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摘要

ARR19 (androgen receptor corepressor of 19 kDa), which encodes for a leucine-rich protein, is expressed abundantly in the testis. Further analyses revealed that ARR19 was expressed in Leydig cells, and its expression was differentially regulated during Leydig cell development. Adenovirus-mediated overexpression of ARR19 in Leydig cells inhibited testicular steroidogenesis, down-regulating the expression of steroidogenic enzymes, which suggests that ARR19 is an antisteroidogenic factor. Interestingly, cAMP/luteinizing hormone attenuated ARR19 expression in a fashion similar to that of GATA-1, which was previously reported to be down-regulated by cAMP. Sequence analysis of the Arr19 promoter revealed the presence of two putative GATA-1 binding motifs. Further analyses with 5′ deletion and point mutants of putative GATA-1 binding motifs showed that these GATA-1 binding sites were critical for high promoter activity. CREB-binding protein coactivated GATA-1 and markedly increased the activity of the Arr19 promoter. Both GATA-1 and CREB-binding proteins occupied the GATA-1 motifs within the Arr19 promoter, which was repressed by cAMP treatment. Altogether, these findings demonstrate that ARR19 is the target gene of GATA-1 and suggest that ARR19 gene expression in testicular Leydig cells is regulated by luteinizing hormone/cAMP signaling via the control of GATA-1 expression, resulting in the control of testicular steroidogenesis.
机译:编码富含亮氨酸的蛋白的ARR19(19 kDa的雄激素受体共加压子)在睾丸中大量表达。进一步的分析表明,ARR19在Leydig细胞中表达,并且在Leydig细胞发育过程中其表达受到差异调节。腺病毒介导的Leydig细胞中ARR19的过量表达抑制了睾丸类固醇生成,下调了类固醇生成酶的表达,这表明ARR19是一种抗类固醇生成因子。有趣的是,cAMP /促黄体生成素以类似于GATA-1的方式减弱了ARR19的表达,以前据报道它被cAMP下调。 Arr19启动子的序列分析揭示了两个推定的GATA-1结合基序的存在。对5'缺失和推定的GATA-1结合基序的点突变体的进一步分析表明,这些GATA-1结合位点对于高启动子活性至关重要。 CREB结合蛋白共激活GATA-1,并显着增加Arr19启动子的活性。 GATA-1和CREB结合蛋白都占据了Arr19启动子内的GATA-1基序,而后者被cAMP处理抑制。总而言之,这些发现表明ARR19是GATA-1的靶基因,并表明睾丸间质细胞中ARR19基因的表达受黄体激素/ cAMP信号转导的调控,从而控制了GATA-1的表达,从而控制了睾丸类固醇的生成。

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