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Cis-regulatory elements explain most of the mRNA stability variation across genes in yeast.

Julien GagneurKerstin C MaierŽiga AvsecPetra RusJulien Gagneur
Published in: RNA (New York, N.Y.) (2017)
The stability of mRNA is one of the major determinants of gene expression. Although a wealth of sequence elements regulating mRNA stability has been described, their quantitative contributions to half-life are unknown. Here, we built a quantitative model for Saccharomyces cerevisiae based on functional mRNA sequence features that explains 59% of the half-life variation between genes and predicts half-life at a median relative error of 30%. The model revealed a new destabilizing 3' UTR motif, ATATTC, which we functionally validated. Codon usage proves to be the major determinant of mRNA stability. Nonetheless, single-nucleotide variations have the largest effect when occurring on 3' UTR motifs or upstream AUGs. Analyzing mRNA half-life data of 34 knockout strains showed that the effect of codon usage not only requires functional decapping and deadenylation, but also the 5'-to-3' exonuclease Xrn1, the nonsense-mediated decay genes, but not no-go decay. Altogether, this study quantitatively delineates the contributions of mRNA sequence features on stability in yeast, reveals their functional dependencies on degradation pathways, and allows accurate prediction of half-life from mRNA sequence.
Keyphrases
  • saccharomyces cerevisiae
  • gene expression
  • binding protein
  • genome wide
  • high resolution
  • escherichia coli
  • dna methylation
  • transcription factor
  • mass spectrometry
  • big data
  • bioinformatics analysis
  • wild type