Desuccinylation of Inosine-5´-monophosphate Dehydrogenase 1 by SIRT5 Promotes Tumor Cell Proliferation.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biological Chemistry Pub Date : 2024-11-08 DOI:10.1016/j.jbc.2024.107976
Chang Xu, Pengbo Yao, Jie Cheng, Peng Jiang
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Abstract

Inosine-5´-monophosphate dehydrogenase (IMPDH) catalyzes the rate limiting step of de novo purine synthesis. Currently, it remains still largely unknown how this metabolic event is regulated in tumor cells. Here, we report that a deacetylase sirtuin 5 (SIRT5) may possess a regulatory effect on GMP anabolism by desuccinylating IMPDH1. We found that SIRT5 can directly interacts with IMPDH1 and promotes desuccinylation on the N terminal of IMPDH1, thereby leading to increased IMPDH enzymatic activity, enhanced purine biosynthesis and promoted cell proliferation. Consistently, down-regulation of SIRT5 expression results in decreased IMPDH1 activity and impaired tumor cell proliferation. Therefore, our results reveal that SIRT5-mediated IMPDH1 desuccinylation adapts purine metabolism for rapid cell growth, and could be a potential therapeutic target for tumor cell proliferation inhibition.

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SIRT5对肌苷-5´-单磷酸脱氢酶1的脱琥珀酰化促进肿瘤细胞增殖
肌苷-5´-单磷酸脱氢酶(IMPDH)催化嘌呤从头合成的限速步骤。目前,这一代谢过程在肿瘤细胞中是如何调控的仍是个未知数。在这里,我们报告了一种去乙酰化酶 SIRT5(sirtuin 5)可能通过去琥珀酰化 IMPDH1 对 GMP 合成代谢具有调控作用。我们发现,SIRT5 可直接与 IMPDH1 相互作用,并促进 IMPDH1 N 端脱琥珀酰化,从而导致 IMPDH 酶活性增加、嘌呤生物合成增强并促进细胞增殖。同样,下调 SIRT5 的表达会导致 IMPDH1 活性降低,肿瘤细胞增殖受阻。因此,我们的研究结果表明,SIRT5 介导的 IMPDH1 去琥珀酰化可使嘌呤代谢适应细胞的快速生长,可能成为抑制肿瘤细胞增殖的潜在治疗靶点。
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Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
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期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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