| Literature DB >> 29931155 |
Dinanath Sulakhe1,2, Mark D'Souza1, Sheng Wang1,3, Sandhya Balasubramanian1,4, Prashanth Athri5, Bingqing Xie1,6, Stefan Canzar3,7, Gady Agam6, T Conrad Gilliam1,2, Natalia Maltsev1,2.
Abstract
In recent years, the emphasis of scientific inquiry has shifted from whole-genome analyses to an understanding of cellular responses specific to tissue, developmental stage or environmental conditions. One of the central mechanisms underlying the diversity and adaptability of the contextual responses is alternative splicing (AS). It enables a single gene to encode multiple isoforms with distinct biological functions. However, to date, the functions of the vast majority of differentially spliced protein isoforms are not known. Integration of genomic, proteomic, functional, phenotypic and contextual information is essential for supporting isoform-based modeling and analysis. Such integrative proteogenomics approaches promise to provide insights into the functions of the alternatively spliced protein isoforms and provide high-confidence hypotheses to be validated experimentally. This manuscript provides a survey of the public databases supporting isoform-based biology. It also presents an overview of the potential global impact of AS on the human canonical gene functions, molecular interactions and cellular pathways.Entities:
Keywords: alternative splicing; context-specific; interaction; isoform; pathway; protein function
Year: 2019 PMID: 29931155 PMCID: PMC6917224 DOI: 10.1093/bib/bby047
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 11.622