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 <i>Methanosarcina acetivorans</i> . All four <i>sri</i> genes are encoded in an operon and each Sri protein inhibits protein synthesis <i>in vitro</i> . Deletion of <i>sri</i> genes in <i>M. acetivorans</i> 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 <i>sri</i> 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.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-19
DOI
https://doi.org/10.64898/2026.01.19.700200
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
22.24
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Dipti D. Nayak, Amos J. Nissley, Yekaterina Shulgina, J.A. Dunkle et al.
1 citations
bioRxiv (Cold Spring Harbor Laboratory)
RNA and protein synthesis mechanisms
22.24
article

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

Dipti D. Nayak, Amos J. Nissley, Yekaterina Shulgina, J.A. Dunkle, Madison C Williams, Roan W. Kivimae
article en
1 citations

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 <i>Methanosarcina acetivorans</i> . All four <i>sri</i> genes are encoded in an operon and each Sri protein inhibits protein synthesis <i>in vitro</i> . Deletion of <i>sri</i> genes in <i>M. acetivorans</i> 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 <i>sri</i> 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.

bioRxiv (Cold Spring Harbor Laboratory)
QB3 (US), Lawrence Berkeley National Laboratory (US), Innovative Genomics Institute (US), University of California, Berkeley (US)
Openalex Percentile: Top 2%
RNA and protein synthesis mechanisms
22.24
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.