AI Article Synopsis

  • * In a study analyzing RNAseq data from different strains, deletion of RofA in M1 strains affected expression levels of several genes, with distinct impacts on each lineage regarding non-pilus genes.
  • * Changes in gene expression due to specific SNPs in the M1 lineage didn't significantly affect an M1 strain, but reversing those SNPs resulted in notable transcriptomic changes similar to those caused by RofA deletion, indicating a complex regulatory role that requires further exploration.

Article Abstract

The standalone regulator RofA is a positive regulator of the pilus locus in . Found in only certain genotypes, RofA has been reported to regulate other virulence factors, although its role in the globally dominant 1 is unclear. Given the recent emergence of a new 1 (M1) toxigenic lineage that is distinguished by three non-synonymous SNPs in , we characterized the regulon in six 1 strains that are representative of the two contemporary major 1 lineages (M1 and M1) using RNAseq analysis, and then determined the specific role of the M1-specific SNPs. Deletion of in three M1 strains led to altered expression of 14 genes, including six non-pilus locus genes. In M1 strains, deletion of led to altered expression of 16 genes, including nine genes that were unique to M1. Only the pilus locus genes were common to the RofA regulons of both lineages, while transcriptomic changes varied between strains even within the same lineage. Although introduction of the three SNPs into did not impact gene expression in an M1 strain, reversal of three SNPs in an M1 strain led to an unexpected number of transcriptomic changes that in part recapitulated transcriptomic changes seen when deleting RofA in the same strain. Computational analysis predicted that interactions with a key histidine residue in the PRD domain of RofA would differ between M1 and M1. RofA is a positive regulator of the pilus locus in all 1 strains but effects on other genes are strain- and lineage-specific, with no clear, common DNA binding motif. The SNPs in that characterize M1 may impact regulation of RofA; whether they alter phosphorylation of the RofA PRD domain requires further investigation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10763501PMC
http://dx.doi.org/10.1099/mgen.0.001159DOI Listing

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