Genome rearrangements can make and break small RNA genes.
- Citation data:
Genome biology and evolution, ISSN: 1759-6653, Vol: 7, Issue: 2, Page: 557-66
- Publication Year:
- Repository URL:
- https://works.bepress.com/rahul-raghavan/40; https://pdxscholar.library.pdx.edu/bio_fac/103
- Agricultural and Biological Sciences; Biochemistry, Genetics and Molecular Biology; Escherichia coli.; Salmonella; RNA; Genomics; Non-coding RNA; Bacterial genomes; Escherichia coli -- Genetics; Salmonella typhimurium -- Genetics; Biology; Genetics and Genomics
Small RNAs (sRNAs) are short, transcribed regulatory elements that are typically encoded in the intergenic regions (IGRs) of bacterial genomes. Several sRNAs, first recognized in Escherichia coli, are conserved among enteric bacteria, but because of the regulatory roles of sRNAs, differences in sRNA repertoires might be responsible for features that differentiate closely related species. We scanned the E. coli MG1655 and Salmonella enterica Typhimurium genomes for nonsyntenic IGRs as a potential source of uncharacterized, species-specific sRNAs and found that genome rearrangements have reconfigured several IGRs causing the disruption and formation of sRNAs. Within an IGR that is present in E. coli but was disrupted in Salmonella by a translocation event is an sRNA that is associated with the FNR/CRP global regulators and influences E. coli biofilm formation. A Salmonella-specific sRNA evolved de novo through point mutations that generated a σ(70) promoter sequence in an IGR that arose through genome rearrangement events. The differences in the sRNA pools among bacterial species have previously been ascribed to duplication, deletion, or horizontal acquisition. Here, we show that genomic rearrangements also contribute to this process by either disrupting sRNA-containing IGRs or creating IGRs in which novel sRNAs may evolve.