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Translational regulation shapes the molecular landscape of complex disease phenotypes
S. Schafer, E. Adami, M. Heinig, KE. Rodrigues, F. Kreuchwig, J. Silhavy, S. van Heesch, D. Simaite, N. Rajewsky, E. Cuppen, M. Pravenec, M. Vingron, SA. Cook, N. Hubner,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
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PubMed
26007203
DOI
10.1038/ncomms8200
Knihovny.cz E-resources
- MeSH
- Phenotype MeSH
- Hypertension metabolism MeSH
- Liver metabolism MeSH
- Myocardium metabolism MeSH
- Rats, Inbred BN MeSH
- Rats, Inbred SHR MeSH
- Proteome MeSH
- Gene Expression Regulation * MeSH
- Ribosomes metabolism MeSH
- Sequence Analysis, RNA MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The extent of translational control of gene expression in mammalian tissues remains largely unknown. Here we perform genome-wide RNA sequencing and ribosome profiling in heart and liver tissues to investigate strain-specific translational regulation in the spontaneously hypertensive rat (SHR/Ola). For the most part, transcriptional variation is equally apparent at the translational level and there is limited evidence of translational buffering. Remarkably, we observe hundreds of strain-specific differences in translation, almost doubling the number of differentially expressed genes. The integration of genetic, transcriptional and translational data sets reveals distinct signatures in 3'UTR variation, RNA-binding protein motifs and miRNA expression associated with translational regulation of gene expression. We show that a large number of genes associated with heart and liver traits in human genome-wide association studies are primarily translationally regulated. Capturing interindividual differences in the translated genome will lead to new insights into the genes and regulatory pathways underlying disease phenotypes.
References provided by Crossref.org
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