# Genetic constraints on protein loop evolution: out-of-frame stop codons limit Bacillus subtilis stationary-phase mutagenesis

## TL;DR

Out-of-frame stop codons in DNA reduce the likelihood of indel mutations in protein loops, limiting genetic variation and evolution in Bacillus subtilis.

## Contribution

This study provides the first in vivo evidence that out-of-frame stop codons restrict indel mutations and protein evolution in protein loops.

## Key findings

- Strains with out-of-frame stop codons had lower indel frequencies compared to those without.
- Indels in strains without out-of-frame stop codons produced more amino acid variation in protein loops.
- Indel formation depends on the transcription-coupled repair factor Mfd and increases with transcription levels.

## Abstract

Insertion and deletion (indel) 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) which may restrict OSC frameshifts from becoming non-functional 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 the formation of indel mutations in DNA encoding the Bacillus 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, respectively). 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. Furthermore, 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 that 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 the presence of homopolymers. Indel formation was dependent on the transcription-coupled repair factor Mfd and increased with elevated transcription. In addition to promoting the premature translation termination of non-functional peptides, this study provides the first in vivo evidence that OSCs are DNA features that restrict genetic changes and constrict the evolution of new protein domains like those that evolve from protein loops.