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Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):E2792-801. doi: 10.1073/pnas.1222534110. Epub 2013 Jul 5.

Deciphering the rules by which 5'-UTR sequences affect protein expression in yeast.

Author information

1
Departments of Computer Science and Applied Mathematics, Weizmann Institute of Science, Rehovot 76100, Israel.

Abstract

The 5'-untranslated region (5'-UTR) of mRNAs contains elements that affect expression, yet the rules by which these regions exert their effect are poorly understood. Here, we studied the impact of 5'-UTR sequences on protein levels in yeast, by constructing a large-scale library of mutants that differ only in the 10 bp preceding the translational start site of a fluorescent reporter. Using a high-throughput sequencing strategy, we obtained highly accurate measurements of protein abundance for over 2,000 unique sequence variants. The resulting pool spanned an approximately sevenfold range of protein levels, demonstrating the powerful consequences of sequence manipulations of even 1-10 nucleotides immediately upstream of the start codon. We devised computational models that predicted over 70% of the measured expression variability in held-out sequence variants. Notably, a combined model of the most prominent features successfully explained protein abundance in an additional, independently constructed library, whose nucleotide composition differed greatly from the library used to parameterize the model. Our analysis reveals the dominant contribution of the start codon context at positions -3 to -1, mRNA secondary structure, and out-of-frame upstream AUGs (uAUGs) to phenotypic diversity, thereby advancing our understanding of how protein levels are modulated by 5'-UTR sequences, and paving the way toward predictably tuning protein expression through manipulations of 5'-UTRs.

KEYWORDS:

AUG sequence context; computational prediction; mRNA folding; post-transcriptional regulation; upstream start codons

PMID:
23832786
PMCID:
PMC3725075
DOI:
10.1073/pnas.1222534110
[Indexed for MEDLINE]
Free PMC Article

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