| Literature DB >> 32343944 |
Nadra Al-Husini1, Dylan T Tomares2, Zechariah J Pfaffenberger3, Nisansala S Muthunayake1, Mohammad A Samad1, Tiancheng Zuo3, Obaidah Bitar1, James R Aretakis1, Mohammed-Husain M Bharmal1, Alisa Gega1, Julie S Biteen3, W Seth Childers4, Jared M Schrader5.
Abstract
Biomolecular condensates play a key role in organizing RNAs and proteins into membraneless organelles. Bacterial RNP-bodies (BR-bodies) are a biomolecular condensate containing the RNA degradosome mRNA decay machinery, but the biochemical function of such organization remains poorly defined. Here, we define the RNA substrates of BR-bodies through enrichment of the bodies followed by RNA sequencing (RNA-seq). We find that long, poorly translated mRNAs, small RNAs, and antisense RNAs are the main substrates, while rRNA, tRNA, and other conserved non-coding RNAs (ncRNAs) are excluded from these bodies. BR-bodies stimulate the mRNA decay rate of enriched mRNAs, helping to reshape the cellular mRNA pool. We also observe that BR-body formation promotes complete mRNA decay, avoiding the buildup of toxic endo-cleaved mRNA decay intermediates. The combined selective permeability of BR-bodies for both enzymes and substrates together with the stimulation of the sub-steps of mRNA decay provide an effective organization strategy for bacterial mRNA decay.Entities:
Keywords: BR-bodies; RNP granules; Ribonuclease E; biomolecular condensates; mRNA decay; phase separation; ribonucleoprotein
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Year: 2020 PMID: 32343944 PMCID: PMC7245546 DOI: 10.1016/j.molcel.2020.04.001
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970