G protein-coupled oestrogen receptor regulates branched-chain amino acid metabolism through c-Jun N-terminal kinase

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Anshu Gupta, Prasad Govind Shinde, Sachin Jorvekar, Akash Suresh Humane, Mythri Chandrasekaran, Roshan M. Borkar, Sudhagar Selvaraju
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引用次数: 0

Abstract

Branched-chain amino acids (BCAA) are essential requirements for overall protein turnover, signalling and energy balance, and dysregulation of their metabolic pathway has been associated with many pathophysiological events. Despite the importance of BCAA in human health, our understanding of their metabolic regulation is limited. Here, we present evidence that G protein-coupled oestrogen receptor (GPER) activation inhibits the key BCAA metabolic regulatory enzyme branched-chain α-keto acid dehydrogenase complex (BCKDH) by phosphorylating S293. Inhibition of BCKDH results in leucine, isoleucine and valine accumulation in cells. Interestingly, GPER did not alter the levels of the kinase BCKDK and the phosphatase PPM1K, which regulate BCKDH activity, but activated MAPK signalling. Using gene silencing, we identified that JNK intercedes GPER-mediated BCKDH inhibition. Together, our results demonstrate that GPER inhibits BCAA metabolism through JNK signalling.

Abstract Image

G蛋白偶联雌激素受体通过c-Jun n-末端激酶调控支链氨基酸代谢。
支链氨基酸(BCAA)是整体蛋白质周转、信号传导和能量平衡的必需物质,其代谢途径的失调与许多病理生理事件有关。尽管支链氨基酸在人体健康中的重要性,我们对其代谢调节的理解是有限的。在这里,我们提出证据,G蛋白偶联雌激素受体(GPER)激活通过磷酸化S293抑制关键的BCAA代谢调节酶支链α-酮酸脱氢酶复合物(BCKDH)。抑制BCKDH导致亮氨酸、异亮氨酸和缬氨酸在细胞中积累。有趣的是,GPER没有改变调节BCKDH活性的激酶BCKDK和磷酸酶PPM1K的水平,但激活了MAPK信号传导。通过基因沉默,我们发现JNK介导gper介导的BCKDH抑制。总之,我们的研究结果表明GPER通过JNK信号传导抑制BCAA代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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