The ubiquitin ligase <scp>RNF115</scp> is required for the clearance of damaged lysosomes

Lysosomes play a critical role in the quality control of cellular organelles. However, lysosomal membranes can be damaged under a variety of conditions, leading to the onset of various diseases. Damaged lysosomes are selectively cleared via a ubiquitin-dependent mechanism, but the molecular mechanisms underlying this process have not been adequately elucidated. In this study, we found that RNF115 is a lysosomal damage-responsive ubiquitin ligase that undergoes massive translocation from the cytosol to the p62/SQSTM1-positive puncta around ruptured lysosomes. In accordance with the changes in its distribution, the depletion of RNF115 delayed the removal of Gal3 from damaged lysosomes during the restoration process following lysosomal damage. These observations suggest that RNF115 is responsible for the clearance of damaged lysosomes.

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Publication Details

Journal
FEBS Letters
Published
2026-04-24
DOI
https://doi.org/10.1002/1873-3468.70346
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
0.00

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article

The ubiquitin ligase RNF115 is required for the clearance of damaged lysosomes

Akiko Kuma, Sae Nakanaga, Hiroyuki Kawahara, Toshiki Takahashi
FEBS Letters
Autophagy in Disease and Therapy
article

The ubiquitin ligase RNF115 is required for the clearance of damaged lysosomes

Akiko Kuma, Sae Nakanaga, Hiroyuki Kawahara, Toshiki Takahashi
article en

Abstract

Lysosomes play a critical role in the quality control of cellular organelles. However, lysosomal membranes can be damaged under a variety of conditions, leading to the onset of various diseases. Damaged lysosomes are selectively cleared via a ubiquitin-dependent mechanism, but the molecular mechanisms underlying this process have not been adequately elucidated. In this study, we found that RNF115 is a lysosomal damage-responsive ubiquitin ligase that undergoes massive translocation from the cytosol to the p62/SQSTM1-positive puncta around ruptured lysosomes. In accordance with the changes in its distribution, the depletion of RNF115 delayed the removal of Gal3 from damaged lysosomes during the restoration process following lysosomal damage. These observations suggest that RNF115 is responsible for the clearance of damaged lysosomes.

FEBS Letters
Osaka Health Science University (JP), Tokyo Metropolitan University (JP)
Takeda Science Foundation, Japan Society for the Promotion of Science
Life in Land
Openalex Percentile: Top 6%
Autophagy in Disease and Therapy
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