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Y染色体上的SRY基因对单胺氧化酶A的调控。

Regulation of monoamine oxidase A by the SRY gene on the Y chromosome.

作者信息

Wu Jason B, Chen Kevin, Li Yunmin, Lau Yun-Fai Chris, Shih Jean C

机构信息

Department of Pharmacology, School of Pharmacy, University of Southern California, 1985 Zonal Ave., PSC 518, Los Angeles, CA 90089-9121, USA.

出版信息

FASEB J. 2009 Nov;23(11):4029-38. doi: 10.1096/fj.09-139097. Epub 2009 Aug 6.

Abstract

Monoamine oxidase A (MAO A), encoded by the X chromosome, catalyzes the oxidative deamination of monoamine neurotransmitters, such as serotonin, and plays a critically important role in brain development and functions. Abnormal MAO A activity has been implicated in several neuropsychiatric disorders, such as depression, autism, and attention deficit hyperactivity disorder, which show sexual dimorphism. However, the molecular basis for these disease processes is unclear. Recently, we found that MAO A was a putative target gene directly regulated by a transcription factor encoded by the sex-determining region Y (SRY) gene located on the Y chromosome. We demonstrated that SRY activates both MAO A-promoter and catalytic activities in a human male neuroblastoma BE(2)C cell line. A functional SRY-binding site in the MAO A core promoter was identified and validated by electrophoretic mobility shift and chromatin immunoprecipitation (ChIP) analyses. Coimmunoprecipitation and ChIP assays showed that SRY and Sp1 form a transcriptional complex and synergistically activate MAO A transcription. This is the first study demonstrating that the Y-encoded transcription factor SRY is capable of regulating an X-located gene, suggesting a novel molecular mechanism for sexual dimorphism in neural development, brain functions, and initiation/progression of neural disorders associated with MAO A dysfunction.

摘要

单胺氧化酶A(MAO A)由X染色体编码,催化单胺神经递质(如血清素)的氧化脱氨反应,并在大脑发育和功能中发挥至关重要的作用。MAO A活性异常与多种神经精神疾病有关,如抑郁症、自闭症和注意力缺陷多动障碍,这些疾病存在性别差异。然而,这些疾病过程的分子基础尚不清楚。最近,我们发现MAO A是位于Y染色体上的性别决定区域Y(SRY)基因编码的转录因子直接调控的一个假定靶基因。我们证明,SRY在人男性神经母细胞瘤BE(2)C细胞系中激活MAO A启动子和催化活性。通过电泳迁移率变动分析和染色质免疫沉淀(ChIP)分析鉴定并验证了MAO A核心启动子中的一个功能性SRY结合位点。免疫共沉淀和ChIP分析表明,SRY和Sp1形成转录复合物并协同激活MAO A转录。这是第一项证明Y编码的转录因子SRY能够调控位于X染色体上的基因的研究,提示了神经发育、脑功能以及与MAO A功能障碍相关的神经疾病的发生/进展中性别差异的一种新分子机制。

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