PreprintCited by 41Bacterial Genetics and BiotechnologyGenomics and Phylogenetic StudiesEvolution and Genetic Dynamics

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Intragenic DNA inversions expand bacterial coding capacity

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Preprint — published as 10.1038/s41586-024-07970-4

Abstract

Bacterial populations that originate from a single bacterium are not strictly clonal. Often, they contain subgroups with distinct phenotypes. Bacteria can generate heterogeneity through phase variation: a preprogrammed, reversible mechanism that alters gene expression levels across a population. One well studied type of phase variation involves enzyme-mediated inversion of specific intergenic regions of genomic DNA. Frequently, these DNA inversions flip the orientation of promoters, turning ON or OFF adjacent coding regions within otherwise isogenic populations. Through this mechanism, inversion can affect fitness, survival, or group dynamics. Here, we develop and apply bioinformatic approaches to discover thousands of previously undescribed phase-variable regions in prokaryotes using long-read datasets. We identify ‘intragenic invertons’, a surprising new class of invertible elements found entirely within genes, in bacteria and archaea. To date, inversions within single genes have not been described. Intragenic invertons allow a gene to encode two or more versions of a protein by flipping a DNA sequence within the coding region, thereby increasing coding capacity without increasing genome size. We experimentally characterize specific intragenic invertons in the gut commensal Bacteroides thetaiotaomicron , presenting a ‘roadmap’ for investigating this new gene-diversifying phenomenon. One-Sentence Summary: Intragenic DNA inversions, identified using long-read sequencing datasets, are found in many phyla across the prokaryotic tree of life.

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Metadata

Authors
Chanin, R. B., West, P. T., Park, R. M., Wirbel, J., Green, G. Z. M., Miklos, A. M., Gill, M. O., Hickey, A. S., Brooks, E. F., & Bhatt, A. S.
Affiliations
  • Stanford Medicine (US)
  • Stanford University (US)
Corresponding author
Bhatt, Ami S.
Venue
Nature
Publisher
openRxiv
Published
2023-03-11
Volume
634
Issue
8032
Pages
234-242
ISSN
0028-0836 (ISSN-L)
OpenAlex
W4402826747
Cited by
41
References
1
Citations by year
2026: 12 · 2025: 20 · 2024: 8 · 2023: 1
FWCI
10.57
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Nature (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • PubMed Central (submittedVersion, cc-by-nc-nd)
  • RePEc: Research Papers in Economics (submittedVersion)
Funders
  • National Institutes of Health (TL1TR003019)
  • National Heart, Lung, and Blood Institute (T32HL120824)
  • National Human Genome Research Institute (K22HG000044, T32HG000044)
  • National Institute of Allergy and Infectious Diseases (R01AI148623, R01AI143757)
  • National Center for Advancing Translational Sciences
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
Keywords
phase variation, long-read sequencing, Bacteroides thetaiotaomicron, ThiC, thiamine biosynthesis, archaea, protein isoforms, gut commensal bacteria

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