4.8 Article

Rare ribosomal RNA sequences from archaea stabilize the bacterial ribosome

Journal

NUCLEIC ACIDS RESEARCH
Volume 51, Issue 4, Pages 1880-1894

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkac1273

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Research discovers that Thermoproteota, a phylum of thermophilic Archaea, uses cytidine to replace uridine in the A loop, stabilizing the ribosome at high temperatures and protecting its catalytic function of peptide bond formation.
The ribosome serves as the universally conserved translator of the genetic code into proteins and supports life across diverse temperatures ranging from below freezing to above 120 degrees C. Ribosomes are capable of functioning across this wide range of temperatures even though the catalytic site for peptide bond formation, the peptidyl transferase center, is nearly universally conserved. Here we find that Thermoproteota, a phylum of thermophilic Archaea, substitute cytidine for uridine at large subunit rRNA positions 2554 and 2555 (Escherichia coli numbering) in the A loop, immediately adjacent to the binding site for the 3 '-end of A-site tRNA. We show by cryo-EM that E. coli ribosomes with uridine to cytidine mutations at these positions retain the proper fold and post-transcriptional modification of the A loop. Additionally, these mutations do not affect cellular growth, protect the large ribosomal subunit from thermal denaturation, and increase the mutational robustness of nucleotides in the peptidyl transferase center. This work identifies sequence variation across archaeal ribosomes in the peptidyl transferase center that likely confers stabilization of the ribosome at high temperatures and develops a stable mutant bacterial ribosome that can act as a scaffold for future ribosome engineering efforts.

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