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SETD2 通过甲基化 FIP200 来防止 Trim21 诱导的降解并维持自噬起始。

FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation.

机构信息

Center for Genomic and Precision Medicine, Institute of Biosciences and Technology, Texas A&M University, Houston, TX 77030, USA.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

出版信息

Cells. 2022 Oct 22;11(21):3333. doi: 10.3390/cells11213333.

Abstract

FIP200, also known as RB1CC1, is a protein that assembles the autophagy initiation complex. Its post-translational modifications and degradation mechanisms are unclear. Upon autophagy activation, we find that FIP200 is methylated at lysine1133 (K1133) by methyltransferase SETD2. We identify the E3 ligase Trim21 to be responsible for FIP200 ubiquitination by targeting K1133, resulting in FIP200 degradation through the ubiquitin-proteasome system. SETD2-induced methylation blocks Trim21-mediated ubiquitination and degradation, preserving autophagy activity. SETD2 and Trim21 orchestrate FIP200 protein stability to achieve dynamic and precise control of autophagy flux.

摘要

FIP200,也称为 RB1CC1,是一种组装自噬起始复合物的蛋白质。其翻译后修饰和降解机制尚不清楚。在自噬激活时,我们发现 FIP200 被甲基转移酶 SETD2 甲基化在赖氨酸 1133(K1133)。我们确定 E3 连接酶 Trim21 通过靶向 K1133 负责 FIP200 的泛素化,导致 FIP200 通过泛素-蛋白酶体系统降解。SETD2 诱导的甲基化阻止了 Trim21 介导的泛素化和降解,从而保持自噬活性。SETD2 和 Trim21 协调 FIP200 蛋白稳定性,以实现自噬流的动态和精确控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d904/9653720/1e5d49b3c440/cells-11-03333-g001.jpg

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