AI Article Synopsis

  • - The study focuses on ribosomal RNA (rRNA) modifications in prokaryotes, particularly gram-positive bacteria, using a model organism that has a well-documented genome but lacks a complete characterization of its rRNA modifications.
  • - Researchers utilized advanced mass spectrometry methods to identify 25 specific rRNA modification sites in the 16S and 23S rRNA, including details on the chemical nature and exact locations of these modifications.
  • - The findings shed light on rRNA modification patterns and establish a framework for future studies on the role of these modifications in ribosome assembly and function, following similar comprehensive annotations in other bacterial species.

Article Abstract

Ribosomal RNA modifications in prokaryotes have been sporadically studied, but there is a lack of a comprehensive picture of modification sites across bacterial phylogeny. is a preeminent model organism for gram-positive bacteria, with a well-annotated and editable genome, convenient for fundamental studies and industrial use. Yet remarkably, there has been no complete characterization of its rRNA modification inventory. By expanding modern MS tools for the discovery of RNA modifications, we found a total of 25 modification sites in 16S and 23S rRNA of including the chemical identity of the modified nucleosides and their precise sequence location. Furthermore, by perturbing large subunit biogenesis using depletion of an essential factor RbgA and measuring the completion of 23S modifications in the accumulated intermediate, we provide a first look at the order of modification steps during the late stages of assembly in . While our work expands the knowledge of bacterial rRNA modification patterns, adding to the list of fully annotated species after and in a broader context, it provides the experimental framework for discovery and functional profiling of rRNA modifications to ultimately elucidate their role in ribosome biogenesis and translation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11100780PMC
http://dx.doi.org/10.1101/2024.05.10.593627DOI Listing

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