SETD7 promotes LC3B methylation and degradation in ovarian cancer

Microtubule-associated protein 1 light chain 3 (LC3) is a key autophagy-related protein involved in regulating autophagosome formation and autophagy activity. Post-translational modifications of LC3 are necessary to modulate its function. However, LC3 protein methylation and its physiological significance have not yet been elucidated. Here, we show that SET domain containing lysine methyltransferase 7 (SETD7) interacts with LC3B, a common isoform of LC3, and methylates LC3B at lysine 51 (K51). SETD7-mediated methylation of LC3B promotes ubiquitination and degradation of LC3B, resulting in reduced autophagosome formation. Furthermore, SETD7 exerts a tumor-promotive function in ovarian cancer (OC) cells in a K51 methylation-dependent manner. Collectively, our data define a novel modification of LC3B and highlight the oncogenic effect of SETD7 via mediating LC3B methylation and degradation.

Authors

Institutions

Publication Details

Journal
Journal of Biological Chemistry
Published
2024-12-25
DOI
https://doi.org/10.1016/j.jbc.2024.108134
Citations
3
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.70

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

SETD7 promotes LC3B methylation and degradation in ovarian cancer

Yanan Hou, Ting Huang, Bowen Zhang, Ziwei Zhang et al.
3 citations
Journal of Biological Chemistry
Ubiquitin and proteasome pathways
0.70
article

SETD7 promotes LC3B methylation and degradation in ovarian cancer

Yanan Hou, Ting Huang, Bowen Zhang, Ziwei Zhang, Genbao Shao, Mingyang Li, Qiong Lin
article en
3 citations

Abstract

Microtubule-associated protein 1 light chain 3 (LC3) is a key autophagy-related protein involved in regulating autophagosome formation and autophagy activity. Post-translational modifications of LC3 are necessary to modulate its function. However, LC3 protein methylation and its physiological significance have not yet been elucidated. Here, we show that SET domain containing lysine methyltransferase 7 (SETD7) interacts with LC3B, a common isoform of LC3, and methylates LC3B at lysine 51 (K51). SETD7-mediated methylation of LC3B promotes ubiquitination and degradation of LC3B, resulting in reduced autophagosome formation. Furthermore, SETD7 exerts a tumor-promotive function in ovarian cancer (OC) cells in a K51 methylation-dependent manner. Collectively, our data define a novel modification of LC3B and highlight the oncogenic effect of SETD7 via mediating LC3B methylation and degradation.

Journal of Biological ChemistryVol. 301(2)
Jiangsu University (CN)
National Natural Science Foundation of China, Government of Jiangsu Province, Jiangsu Provincial Key Research and Development Program
Zero hunger
Openalex Percentile: Top 28%
Ubiquitin and proteasome pathways
0.70
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.