ORIGINAL RESEARCH article
Front. Mol. Biosci.
Sec. Genome Organization and Dynamics
This article is part of the Research TopicMicrobial growth and post-exponential processes: implications for pathogenesis, survival and evolutionView all 3 articles
Genetic Constraints on Protein Loop Evolution: Out-of-Frame Stop Codons limit Bacillus subtilis Stationary-phase mutagenesis
Provisionally accepted- 1NYU Langone Health, New York, United States
- 2Universidad de Guanajuato, Guanajuato, Mexico
- 3University of Nevada, Las Vegas, Las Vegas, United States
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Insertion and deletion (indels) events in protein-coding DNA are associated with loss-of-function frameshift mutations. In silico studies have found that protein coding regions are littered with out-of-frame stop codons (OSCs), and that OSCs may restrict frameshifts from becoming nonfunctional polypeptides by prematurely terminating translation. However, the effect of OSCs on protein variation has not been tested in vivo, specifically when OSCs are found in coding regions characterized by relaxed selection like protein loops. Here, we examined formation of indel mutations in DNA encoding the B. subtilis loop region of the ornithine carbamoyltransferase (Otc) protein by constructing a gain-of-function genetic system in strains with or without OSCs (+OSC and -OSC).The use of a gain-of-function selection system and a DNA region coding for a protein loop in which a wide spectrum of amino acids can restore function allowed us to maximize the spectrum of indels we could detect. We found that the +OSC strain had a lower indel frequency than the -OSC strain. Further, indel events in the -OSC strain were not possible in the +OSC strain because they would shift the OSC into frame and terminate translation. By analyzing all indel events in both background strains, we found the -OSC strain had a broader indel spectrum and led to more amino acid variation in the protein loop of Otc than did the +OSC strain. This variation was not due to GC content or presence of homopolymers. Indel formation was dependent on the transcription-coupled repair factor Mfd and increased with elevated transcription. In addition to promoting premature translation termination of non-functional peptides, this work provides the first in vivo evidence that OSCs are DNA features that restrict genetic changes and constrict evolution of new protein domains like those that evolve from protein loops.
Keywords: frameshift mutation, Microbiology, Mutagenesis, protein evolution, Transcription-coupling repair factor
Received: 26 Sep 2025; Accepted: 22 Jan 2026.
Copyright: © 2026 Vallin, Pedraza-Reyes and Robleto. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Carmen Vallin
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