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Updated: Nov 11, 2025

Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling
Published on: October 7, 2021
Non-essential ribosomal proteins in bacteria and archaea identified using COGs
Michael Y Galperin1, Yuri I Wolf2, Sofya K Garushyants2
1National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20894, USA galperin@ncbi.nlm.nih.gov koonin@ncbi.nlm.nih.gov.
Many ribosomal protein (RP) genes are missing in prokaryotes, especially in smaller genomes. RP loss is linked to their position on the ribosome and late assembly, impacting microbial evolution.
Area of Science:
- Molecular Biology
- Evolutionary Biology
- Genomics
Background:
- Ribosomal proteins (RPs) are crucial for bacterial and archaeal survival, yet many genomes lack certain RP genes.
- Previous studies indicated that some RP gene deletions have minimal impact on bacterial growth.
- Prokaryotic genomes exhibit significant variation in RP gene content, with some RPs being non-essential.
Purpose of the Study:
- To systematically analyze the evolutionary conservation and genuine loss of ribosomal protein genes in prokaryotes.
- To identify trends in RP gene loss related to ribosome architecture and assembly.
- To understand the evolutionary constraints and patterns of ribosome evolution in bacteria and archaea.
Main Methods:
- Compiled a list of missing ribosomal genes from the Clusters of Orthologous Genes (COG) database (1,309 prokaryotic genomes).
- Distinguished genuine gene losses from annotation errors and frameshifts.
- Correlated RP gene loss with experimental data on non-essential RPs in model organisms (E. coli, B. subtilis).
Main Results:
- Approximately half of all RPs are universally conserved; up to 16 RPs are missing in some prokaryotic genomes.
- Genuine RP gene losses are prevalent, particularly in small genomes (<1 Mb) of host-associated bacteria and archaea.
- Frequently lost RPs are located on the ribosome periphery and are often non-essential, showing overlap between computational and experimental findings.
Conclusions:
- Ribosome architecture and assembly order influence RP essentiality and susceptibility to gene loss.
- RPs on the ribosome surface or incorporated late in assembly are more prone to loss during genome compaction.
- Identified common trends and constraints in prokaryotic ribosome evolution, particularly in symbiotic and parasitic lineages.
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