Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans
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- 5 May 2009
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 106 (18) , 7507-7512
- https://doi.org/10.1073/pnas.0810916106
Abstract
Upstream ORFs (uORFs) are mRNA elements defined by a start codon in the 5′ UTR that is out-of-frame with the main coding sequence. Although uORFs are present in approximately half of human and mouse transcripts, no study has investigated their global impact on protein expression. Here, we report that uORFs correlate with significantly reduced protein expression of the downstream ORF, based on analysis of 11,649 matched mRNA and protein measurements from 4 published mammalian studies. Using reporter constructs to test 25 selected uORFs, we estimate that uORFs typically reduce protein expression by 30–80%, with a modest impact on mRNA levels. We additionally identify polymorphisms that alter uORF presence in 509 human genes. Finally, we report that 5 uORF-altering mutations, detected within genes previously linked to human diseases, dramatically silence expression of the downstream protein. Together, our results suggest that uORFs influence the protein expression of thousands of mammalian genes and that variation in these elements can influence human phenotype and disease.Keywords
This publication has 51 references indexed in Scilit:
- Genome-Wide Analysis in Vivo of Translation with Nucleotide Resolution Using Ribosome ProfilingScience, 2009
- A Mitochondrial Protein Compendium Elucidates Complex I Disease BiologyCell, 2008
- Comprehensive and quantitative proteome profiling of the mouse liver and plasmaHepatology, 2008
- 28-Way vertebrate alignment and conservation track in the UCSC Genome BrowserGenome Research, 2007
- Integrated proteomic and transcriptomic profiling of mouse lung development and Nmyc target genesMolecular Systems Biology, 2007
- The molecular basis of familial hypercholesterolaemia in Turkish patientsAtherosclerosis, 2005
- A gene atlas of the mouse and human protein-encoding transcriptomesProceedings of the National Academy of Sciences, 2004
- Human Gene Mutation Database (HGMD®): 2003 updateHuman Mutation, 2003
- The UCSC Genome Browser DatabaseNucleic Acids Research, 2003
- Mutation in the 5′ noncoding region of the SRY gene in an XY sex-reversed patientHuman Mutation, 1998