Proteomic composition of eukaryotic and bacterial RNA decay condensates suggests convergent evolution.

Curr Opin Microbiol

Wayne State University, Department of Biological Sciences, Detroit, MI, USA. Electronic address:

Published: June 2024

AI Article Synopsis

  • Bacterial cells organize their cytoplasm using biomolecular condensates (BMCs), which are nonmembrane-bound organelles formed through phase separation.
  • Bacterial ribonucleoprotein bodies (BR-bodies) are a key example of BMCs that house RNA decay machinery, showing functional similarities to eukaryotic structures like P-bodies and stress granules.
  • Despite differences in mRNA decay processes, recent studies indicate evolutionary convergence in the types of enzymes found in these condensates across bacteria and eukaryotes.

Article Abstract

Bacterial cells have a unique challenge to organize their cytoplasm without the use of membrane-bound organelles. Biomolecular condensates (henceforth BMCs) are a class of nonmembrane-bound organelles, which, through the physical process of phase separation, can form liquid-like droplets with proteins/nucleic acids. BMCs have been broadly characterized in eukaryotic cells, and BMCs have been recently identified in bacteria, with the first and best studied example being bacterial ribonucleoprotein bodies (BR-bodies). BR-bodies contain the RNA decay machinery and show functional parallels to eukaryotic P-bodies (PBs) and stress granules (SGs). Due to the finding that mRNA decay machinery is compartmentalized in BR-bodies and in eukaryotic PBs/SGs, we will explore the functional similarities in the proteins, which are known to enrich in these structures based on recent proteomic studies. Interestingly, despite the use of different mRNA decay and post-transcriptional regulatory machinery, this analysis has revealed evolutionary convergence in the classes of enriched enzymes in these structures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11162941PMC
http://dx.doi.org/10.1016/j.mib.2024.102467DOI Listing

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