Crosstalk between the ribosome quality control‐associated <scp>E3</scp> ubiquitin ligases <scp>LTN1</scp> and <scp>RNF10</scp>

During gene expression, ribosome stalling frequently occurs and can lead to detrimental effects on cellular homeostasis. Several quality control mechanisms, including ribosome-associated quality control (RQC) and nonfunctional ribosomal RNA decay (NRD), have been identified to resolve these aberrant translation events. While the molecular mechanisms of each pathway have been extensively characterized, the mechanisms underlying the mutual regulation of the expression of pathway factors remain to be elucidated. Here, we employed a series of knockout mouse and human cell lines to investigate the crosstalk between translational quality control factors. Our findings revealed that the E3 ubiquitin ligase LTN1 suppresses expression of the E3 ubiquitin ligase RNF10 in a manner dependent on the RING domain of LTN1. This discovery offers new insights into the coordination of translational surveillance pathways.

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Publication Details

Journal
FEBS Letters
Published
2025-12-26
DOI
https://doi.org/10.1002/1873-3468.70230
Citations
1
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.81

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article

Crosstalk between the ribosome quality control‐associated E3 ubiquitin ligases LTN1 and RNF10

Satoru Hashimoto, Kiyoshi Yamaguchi, Yoichi Furukawa, Chisato Kikuguchi et al.
1 citations
FEBS Letters
RNA modifications and cancer
0.81
article

Crosstalk between the ribosome quality control‐associated E3 ubiquitin ligases LTN1 and RNF10

Satoru Hashimoto, Kiyoshi Yamaguchi, Yoichi Furukawa, Chisato Kikuguchi, Toshifumi Inada, Sota Ito, Miho Hoshi, Yuxi Huang, Toru Suzuki
article en
1 citations

Abstract

During gene expression, ribosome stalling frequently occurs and can lead to detrimental effects on cellular homeostasis. Several quality control mechanisms, including ribosome-associated quality control (RQC) and nonfunctional ribosomal RNA decay (NRD), have been identified to resolve these aberrant translation events. While the molecular mechanisms of each pathway have been extensively characterized, the mechanisms underlying the mutual regulation of the expression of pathway factors remain to be elucidated. Here, we employed a series of knockout mouse and human cell lines to investigate the crosstalk between translational quality control factors. Our findings revealed that the E3 ubiquitin ligase LTN1 suppresses expression of the E3 ubiquitin ligase RNF10 in a manner dependent on the RING domain of LTN1. This discovery offers new insights into the coordination of translational surveillance pathways.

FEBS Letters
Systems Biology Institute (JP), The University of Tokyo (JP)
Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, Bundesamt für Gesundheit, University of Tokyo, Japan Society for the Promotion of Science
Openalex Percentile: Top 20%
RNA modifications and cancer
0.81
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