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FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation
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 l...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653720/ https://www.ncbi.nlm.nih.gov/pubmed/36359729 http://dx.doi.org/10.3390/cells11213333 |
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author | Dai, Yuan Luo, Weijia Li, Wenjiao Chen, Zhishi Wang, Xinjie Chang, Jiang |
author_facet | Dai, Yuan Luo, Weijia Li, Wenjiao Chen, Zhishi Wang, Xinjie Chang, Jiang |
author_sort | Dai, Yuan |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9653720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96537202022-11-15 FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation Dai, Yuan Luo, Weijia Li, Wenjiao Chen, Zhishi Wang, Xinjie Chang, Jiang Cells Article 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. MDPI 2022-10-22 /pmc/articles/PMC9653720/ /pubmed/36359729 http://dx.doi.org/10.3390/cells11213333 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dai, Yuan Luo, Weijia Li, Wenjiao Chen, Zhishi Wang, Xinjie Chang, Jiang FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation |
title | FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation |
title_full | FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation |
title_fullStr | FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation |
title_full_unstemmed | FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation |
title_short | FIP200 Methylation by SETD2 Prevents Trim21-Induced Degradation and Preserves Autophagy Initiation |
title_sort | fip200 methylation by setd2 prevents trim21-induced degradation and preserves autophagy initiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653720/ https://www.ncbi.nlm.nih.gov/pubmed/36359729 http://dx.doi.org/10.3390/cells11213333 |
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