Cellular energy regulates mRNA degradation in a codon-specific manner

Mol Syst Biol. 2024 May;20(5):506-520. doi: 10.1038/s44320-024-00026-9. Epub 2024 Mar 15.

Abstract

Codon optimality is a major determinant of mRNA translation and degradation rates. However, whether and through which mechanisms its effects are regulated remains poorly understood. Here we show that codon optimality associates with up to 2-fold change in mRNA stability variations between human tissues, and that its effect is attenuated in tissues with high energy metabolism and amplifies with age. Mathematical modeling and perturbation data through oxygen deprivation and ATP synthesis inhibition reveal that cellular energy variations non-uniformly alter the effect of codon usage. This new mode of codon effect regulation, independent of tRNA regulation, provides a fundamental mechanistic link between cellular energy metabolism and eukaryotic gene expression.

Keywords: mRNA Stability; Cellular Energy Metabolism; Tissue-specific Regulation; Codon Usage Bias; Codon Optimality-mediated mRNA Degradation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Codon Usage
  • Codon* / genetics
  • Energy Metabolism* / genetics
  • Gene Expression Regulation
  • Humans
  • Protein Biosynthesis
  • RNA Stability*
  • RNA, Messenger* / genetics
  • RNA, Messenger* / metabolism
  • RNA, Transfer / genetics
  • RNA, Transfer / metabolism

Substances

  • RNA, Messenger
  • Codon
  • RNA, Transfer
  • Adenosine Triphosphate