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编码的微小蛋白质线粒体调节蛋白在线粒体外膜上调节脂肪酸代谢。

-encoded microprotein mitoregulin regulates fatty acid metabolism at the mitochondrial outer membrane.

作者信息

Zhang Shan, Guo Yabo, Fidelito Gio, Robinson David R L, Liang Chao, Lim Radiance, Bichler Zoë, Guo Ruiyang, Wu Gaoqi, Xu He, Zhou Quan D, Singh Brijesh K, Yen Paul, Kappei Dennis, Stroud David A, Ho Lena

机构信息

Department of Biochemistry, Department of Cardiology of The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310058, China.

Cardiovascular and Metabolic Diseases, Duke-NUS Medical School, Singapore 169857, Singapore.

出版信息

iScience. 2023 Aug 7;26(9):107558. doi: 10.1016/j.isci.2023.107558. eCollection 2023 Sep 15.

Abstract

encodes a microprotein first identified as Mitoregulin (MTLN), where it was reported to localize to the inner membrane of mitochondria to regulate fatty acid oxidation and oxidative phosphorylation. These initial discoveries were followed by reports with differing findings about its molecular functions and submitochondrial localization. To clarify the apparent discrepancies, we constructed multiple orthogonal methods of determining the localization of MTLN, including split GFP-based reporters that enable efficient and reliable topology analyses for microproteins. These methods unequivocally demonstrate MTLN primarily localizes to the outer membrane of mitochondria, where it interacts with enzymes of fatty acid metabolism including CPT1B and CYB5B. Loss of MTLN causes the accumulation of very long-chain fatty acids (VLCFAs), especially docosahexaenoic acid (DHA). Intriguingly, loss of MTLN protects mice against western diet/fructose-induced insulin-resistance, suggests a protective effect of VLCFAs in this context. MTLN thus serves as an attractive target to control the catabolism of VLCFAs.

摘要

它编码一种最初被鉴定为线粒体调节蛋白(MTLN)的微小蛋白,据报道该蛋白定位于线粒体内膜,以调节脂肪酸氧化和氧化磷酸化。这些最初的发现之后,又有关于其分子功能和线粒体亚定位的不同研究结果的报道。为了澄清这些明显的差异,我们构建了多种确定MTLN定位的正交方法,包括基于分裂GFP的报告基因,该报告基因能够对微小蛋白进行高效且可靠的拓扑分析。这些方法明确表明MTLN主要定位于线粒体外膜,在那里它与脂肪酸代谢的酶相互作用,包括肉碱棕榈酰转移酶1B(CPT1B)和细胞色素b5B(CYB5B)。MTLN的缺失会导致极长链脂肪酸(VLCFAs)的积累,尤其是二十二碳六烯酸(DHA)。有趣的是,MTLN的缺失可保护小鼠免受西式饮食/果糖诱导的胰岛素抵抗,这表明在这种情况下VLCFAs具有保护作用。因此,MTLN是控制VLCFAs分解代谢的一个有吸引力的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f6/10469944/e4e15f383761/fx1.jpg

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