Proteomics

Dataset Information

0

Perserverence of protein homeostasis despite mistranslation of glycine codons with alanine


ABSTRACT: By physically linking amino acids to their codon assignments, transfer RNAs (tRNAs) are essential for protein synthesis and translation fidelity. Some natural human tRNA variants cause amino acid mis-incorporation at a codon or set of codons. Recent work showed a naturally occurring tRNASer variant decodes phenylalanine codons with serine and inhibits protein synthesis. We hypothesized that human tRNA variants that mis-read glycine (Gly) codons with alanine (Ala) will disrupt protein homeostasis. The A3G mutation occurs naturally in tRNAGly variants (tRNAGlyCCC, tRNAGlyGCC) and creates an alanyl-tRNA synthetase (AlaRS) identity element (G3:U70). Because AlaRS does not recognize the anticodon, the human tRNAAlaAGC G35C (tRNAAlaACC) variant may function similarly to mis-incorporate Ala at Gly codons. The tRNAGly and tRNAAla variants had no effect on protein synthesis in mammalian cells under normal growth conditions, however, tRNAGlyGCC A3G depressed protein synthesis in the context of proteasome inhibition. Mass spectrometry confirmed Ala mistranslation at several Gly codons caused by the tRNAGlyGCC A3G and tRNAAlaAGC G35C mutants, and in some cases, we observed multiple mistranslation events in the same peptide. The data reveal mistranslation of Ala at Gly codons and defects in protein homeostasis generated by natural human tRNA variants that are tolerated under normal conditions.

INSTRUMENT(S): LTQ Orbitrap Elite

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Brain

SUBMITTER: Farah Hasan  

LAB HEAD: Patrick O'Donoghue

PROVIDER: PXD034180 | Pride | 2024-05-21

REPOSITORIES: Pride

Dataset's files

Source:
altmetric image

Publications

Perseverance of protein homeostasis despite mistranslation of glycine codons with alanine.

Hasan Farah F   Lant Jeremy T JT   O'Donoghue Patrick P  

Philosophical transactions of the Royal Society of London. Series B, Biological sciences 20230111 1871


By linking amino acids to their codon assignments, transfer RNAs (tRNAs) are essential for protein synthesis and translation fidelity. Some human tRNA variants cause amino acid mis-incorporation at a codon or set of codons. We recently found that a naturally occurring tRNA<sup>Ser</sup> variant decodes phenylalanine codons with serine and inhibits protein synthesis. Here, we hypothesized that human tRNA variants that misread glycine (Gly) codons with alanine (Ala) will also disrupt protein homeo  ...[more]

Similar Datasets

2022-02-22 | PXD026636 | Pride
2021-05-11 | GSE174145 | GEO
2022-02-17 | PXD027837 | Pride
2021-05-17 | PXD025934 | Pride
2015-11-06 | GSE65718 | GEO
2024-05-11 | GSE256332 | GEO
2015-11-06 | E-GEOD-65718 | biostudies-arrayexpress
2017-08-03 | PXD005901 | Pride
2022-10-14 | PXD033711 | Pride
2022-08-12 | PXD032063 | Pride