2′-O-Methylation maintains ribosome structural and translation integrity

In eukaryotic ribosomes, ∼2% of RNA nucleotides undergo 2'-O-methylation, a conserved cellular mechanism thought to be critical for maintaining and regulating translation. Here, we use ribosome profiling, translation assays, proteomics, and high-resolution structural analyses to show that loss of native 2'-O-methylation in yeast ribosomes disproportionally affects the translation of ribosomal protein transcripts, driven by changes in codon usage and recognition of structured RNA. Translation reprogramming by the hypomethylated ribosomes is supported by reduced thermostability and high-resolution evidence of altered ribosomal structures and conformations. Consistent with the roles of the affected proteins in sustaining cellular fitness, hypomethylated ribosomes under stress exhibit a selective loss of downregulated proteins and misassembly associated with methylation loss. Our data provide structural and mechanistic insights into how 2'-O-methylation supports ribosome integrity and mediates cellular stress responses.

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Publication Details

Journal
Molecular Cell
Published
2026-04-01
DOI
https://doi.org/10.1016/j.molcel.2026.03.008
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

2′-O-Methylation maintains ribosome structural and translation integrity

Hemant N. Goswami, Jay Rai, Homa Ghalei, Lauren N. Cohen et al.
Molecular Cell
RNA modifications and cancer
article

2′-O-Methylation maintains ribosome structural and translation integrity

Hemant N. Goswami, Jay Rai, Homa Ghalei, Lauren N. Cohen, Yuerong Shu, Hong Li, Hong Jin, Yu Zhao, Xin Chen, Yuri Motorin, Chong Xu, Virginie Marchand
article en

Abstract

In eukaryotic ribosomes, ∼2% of RNA nucleotides undergo 2'-O-methylation, a conserved cellular mechanism thought to be critical for maintaining and regulating translation. Here, we use ribosome profiling, translation assays, proteomics, and high-resolution structural analyses to show that loss of native 2'-O-methylation in yeast ribosomes disproportionally affects the translation of ribosomal protein transcripts, driven by changes in codon usage and recognition of structured RNA. Translation reprogramming by the hypomethylated ribosomes is supported by reduced thermostability and high-resolution evidence of altered ribosomal structures and conformations. Consistent with the roles of the affected proteins in sustaining cellular fitness, hypomethylated ribosomes under stress exhibit a selective loss of downregulated proteins and misassembly associated with methylation loss. Our data provide structural and mechanistic insights into how 2'-O-methylation supports ribosome integrity and mediates cellular stress responses.

Molecular CellVol. 86(8)
Florida State University (US), Centre National de la Recherche Scientifique (FR), Van Andel Institute (US), Emory University (US), Inserm (FR), University of Illinois Urbana-Champaign (US), Université de Lorraine (FR)
U.S. Department of Energy, Simons Foundation, Florida State University, National Institutes of Health, National Institute of General Medical Sciences, Biological and Environmental Research
Openalex Percentile: Top 36%
RNA modifications and cancer
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