AI Article Synopsis

  • Bacteria manage their transition between living in clusters (biofilms) and as free-moving cells by regulating genes linked to biofilm formation through various mechanisms.
  • * RsmA, a post-transcriptional regulator, plays a key role in this process by influencing the stability and translation of certain mRNAs, but its connection to biofilm genes is mostly understood through indirect studies.
  • * The study highlights that RsmA inhibits the transcription factor Vfr, which in turn negatively regulates FleQ, a crucial player in biofilm-associated gene expression, and reveals that RsmA needs the RNA chaperone Hfq to bind to mRNA.

Article Abstract

To appropriately switch between sessile and motile lifestyles, bacteria control expression of biofilm-associated genes through multiple regulatory elements. In , the post-transcriptional regulator RsmA has been implicated in the control of various genes including those related to biofilms, but much of the evidence for these links is limited to transcriptomic and phenotypic studies. RsmA binds to target mRNAs to modulate translation by affecting ribosomal access and/or mRNA stability. Here, we trace a global regulatory role of RsmA to inhibition of the expression of Vfr-a transcription factor that inhibits transcriptional regulator FleQ. FleQ directly controls biofilm-associated genes that encode the PEL polysaccharide biosynthesis machinery. Furthermore, we show that RsmA alone cannot bind mRNA but requires the assistance of RNA chaperone protein Hfq. This is the first example where a RsmA protein family member requires another protein for binding to its target RNA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705225PMC
http://dx.doi.org/10.3389/fmicb.2020.482585DOI Listing

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