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Smad 泛素化调节因子 1 促进 LIM 同源盒基因 9 的降解并抑制间质细胞中睾酮的产生。

Smad ubiquitylation regulatory factor 1 promotes LIM-homeobox gene 9 degradation and represses testosterone production in Leydig cells.

机构信息

Department of Geriatric Endocrinology, Chinese People's Liberation Army General Hospital, National Clinical Research Center for Geriatric Diseases, Beijing, China.

State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center of Protein Sciences, Beijing Institute of Lifeomics, Beijing, China.

出版信息

FASEB J. 2018 Sep;32(9):4627-4640. doi: 10.1096/fj.201701480R. Epub 2018 Mar 22.

Abstract

Testosterone is essential for spermatogenesis and the maintenance of secondary sexual characteristics in males. An important transcription factor, LIM-homeobox gene 9 (Lhx9) is indispensable for testis development and testosterone production; however, post-translational modifications of Lhx9 are largely unknown. Here, for the first time to our knowledge, we demonstrate that the level of Lhx9 protein increases in human chorionic gonadotropin-exposed Leydig cells and can be polyubiquitylated. We found that Smad ubiquitylation regulatory factor 1 (Smurf1), an E3 ubiquitin ligase, targets Lhx9 for ubiquitin-mediated proteasome degradation, thereby negatively modulating its function. Increasing Smurf1 decreases the level of Lhx9 and inhibits the Lhx9 transactivation capacity of steroidogenic factor 1 [nuclear receptor subfamily 5, group A, member 1 (NR5A1)]. In contrast, the depletion of Smurf1 leads to increased expression of Lhx9 protein and enhances testosterone biosynthesis-related gene transcripts [NR5A1, steroidogenic acute regulatory protein, CYP17A1, hydroxy-δ-5-steroid dehydrogenase, hydroxy-δ-5-steroid dehydrogenase isomerase 6, and hydroxysteroid (17-β) dehydrogenase 3] and testosterone production in Leydig cells. Furthermore, we found that Smurf1 knockout mice exhibit higher levels of Lhx9 protein and steroidogenesis, which leads to increased serum testosterone concentration. These findings reveal that Smurf1 promotes Lhx9 ubiquitylation and is involved in testosterone production in Leydig cells directly. Our results provide new insights into the molecular events that play a role in the homeostasis of testosterone levels and may provide a new target for testosterone regulation.-Hu, F., Zhu, Q., Sun, B., Cui, C., Li, C., Zhang, L. Smad ubiquitylation regulatory factor 1 promotes LIM-homeobox gene 9 degradation and represses testosterone production in Leydig cells.

摘要

睾酮对于精子发生和男性的第二性征维持至关重要。LIM 同源盒基因 9(Lhx9)是一种重要的转录因子,对于睾丸发育和睾酮产生不可或缺;然而,Lhx9 的翻译后修饰在很大程度上尚不清楚。在这里,我们首次证明,在人绒毛膜促性腺激素(hCG)暴露的 Leydig 细胞中,Lhx9 蛋白水平增加,并可以被多泛素化。我们发现,Smad 泛素化调节因子 1(Smurf1),一种 E3 泛素连接酶,将 Lhx9 作为泛素介导的蛋白酶体降解的靶标,从而负调控其功能。Smurf1 的增加降低了 Lhx9 的水平,并抑制了类固醇生成因子 1(nuclear receptor subfamily 5, group A, member 1,NR5A1)的 Lhx9 转录激活能力。相反,Smurf1 的耗竭导致 Lhx9 蛋白表达增加,并增强与睾酮生物合成相关的基因转录物[NR5A1、类固醇急性调节蛋白、CYP17A1、羟基-δ-5-类固醇脱氢酶、羟基-δ-5-类固醇脱氢酶异构酶 6 和羟甾醇(17-β)脱氢酶 3]和 Leydig 细胞中的睾酮产生。此外,我们发现 Smurf1 敲除小鼠表现出更高水平的 Lhx9 蛋白和类固醇生成,这导致血清睾酮浓度增加。这些发现表明,Smurf1 促进 Lhx9 的泛素化,并直接参与 Leydig 细胞中的睾酮产生。我们的研究结果提供了关于在维持睾酮水平的动态平衡中发挥作用的分子事件的新见解,并可能为睾酮调节提供新的靶点。-Hu, F., Zhu, Q., Sun, B., Cui, C., Li, C., Zhang, L. Smad ubiquitylation regulatory factor 1 promotes LIM-homeobox gene 9 degradation and represses testosterone production in Leydig cells.

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