Literature DB >> 29931155

Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources.

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.
© The Author(s) 2018. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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


  129 in total

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