| Literature DB >> 26300548 |
Valer Gotea1, Jared J Gartner2, Nouar Qutob3, Laura Elnitski1, Yardena Samuels3.
Abstract
Recent technological advances in sequencing have flooded the field of cancer research with knowledge about somatic mutations for many different cancer types. Most cancer genomics studies focus on mutations that alter the amino acid sequence, ignoring the potential impact of synonymous mutations. However, accumulating experimental evidence has demonstrated clear consequences for gene function, leading to a widespread recognition of the functional role of synonymous mutations and their causal connection to various diseases. Here, we review the evidence supporting the direct impact of synonymous mutations on gene function via gene splicing; mRNA stability, folding, and translation; protein folding; and miRNA-based regulation of expression. These results highlight the functional contribution of synonymous mutations to oncogenesis and the need to further investigate their detection and prioritization for experimental assessment.Entities:
Keywords: cancer; gene splicing; melanoma; miRNA regulation; protein folding; protein translation; secondary structure; synonymous mutations
Mesh:
Year: 2015 PMID: 26300548 PMCID: PMC4834044 DOI: 10.1111/pcmr.12413
Source DB: PubMed Journal: Pigment Cell Melanoma Res ISSN: 1755-1471 Impact factor: 4.693