A family of archaeal hibernation factors that bind in tandem and protect ribosomes in dormant cells

Under nutrient limitation or stress, ribosome hibernation factors inactivate and protect ribosomes. Although ribosome hibernation plays an important role in microbes, we lack a complete understanding of this process in archaea. Here, we identify a family of hibernation factors, which we designate as single ribosomal subunit inhibitors (SriA-SriD), from the methanogenic archaeon Methanosarcina acetivorans. All four sri genes are encoded in an operon and each Sri protein inhibits protein synthesis in vitro. Deletion of sri genes in M. acetivorans impaired growth recovery after prolonged stationary phase and also led to depletion of the small ribosomal subunit. Cryo-EM structures show that Sri proteins bind to the ribosome in tandem and form conserved protein-protein interfaces. Sri is broadly distributed across archaeal phyla and sri genes frequently co-occur. Together, these findings establish Sri proteins as a distinct group of hibernation factors that protect ribosomes during dormancy and expand our understanding of ribosome hibernation in archaea.

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Publication Details

Journal
Nature Communications
Published
2026-06-25
DOI
https://doi.org/10.1038/s41467-026-74727-0
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

A family of archaeal hibernation factors that bind in tandem and protect ribosomes in dormant cells

Dipti D. Nayak, Amos J. Nissley, J.H.D. Cate, Yekaterina Shulgina et al.
Nature Communications
RNA and protein synthesis mechanisms
article

A family of archaeal hibernation factors that bind in tandem and protect ribosomes in dormant cells

Dipti D. Nayak, Amos J. Nissley, J.H.D. Cate, Yekaterina Shulgina, Madison C Williams, Roan W. Kivimae
article en

Abstract

Under nutrient limitation or stress, ribosome hibernation factors inactivate and protect ribosomes. Although ribosome hibernation plays an important role in microbes, we lack a complete understanding of this process in archaea. Here, we identify a family of hibernation factors, which we designate as single ribosomal subunit inhibitors (SriA-SriD), from the methanogenic archaeon Methanosarcina acetivorans. All four sri genes are encoded in an operon and each Sri protein inhibits protein synthesis in vitro. Deletion of sri genes in M. acetivorans impaired growth recovery after prolonged stationary phase and also led to depletion of the small ribosomal subunit. Cryo-EM structures show that Sri proteins bind to the ribosome in tandem and form conserved protein-protein interfaces. Sri is broadly distributed across archaeal phyla and sri genes frequently co-occur. Together, these findings establish Sri proteins as a distinct group of hibernation factors that protect ribosomes during dormancy and expand our understanding of ribosome hibernation in archaea.

Nature Communications
QB3 (US), Lawrence Berkeley National Laboratory (US), Innovative Genomics Institute (US), University of California, Berkeley (US)
National Science Foundation, David and Lucile Packard Foundation, Alfred P. Sloan Foundation, Simons Foundation, Arnold and Mabel Beckman Foundation, Life Sciences Research Foundation, National Institutes of Health, Division of Chemistry
Openalex Percentile: Top 11%
RNA and protein synthesis mechanisms
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