Guan Lab

Department of Computational Medicine & Bioinformatics
Thu, 07/30/2015 - 12:26 -- gyuanfan
TitleFunctional Networks of Highest-Connected Splice Isoforms, from the Chromosome 17 Human Proteome Project.
Publication TypeJournal Article
Year of Publication2015
AuthorsLi H, Menon R, Govindarajoo B, Panwar B, Zhang Y, Omenn GS, Guan Y
JournalJ Proteome Res
Date Published2015 Jul 28
ISSN1535-3907
Abstract

Alternative splicing allows a single gene to produce multiple transcript-level splice isoforms from which the translated proteins may show differences in their expression and function. Identifying the major functional or canonical isoform is important for understanding gene and protein functions. Identification and characterization of splice isoforms is a stated goal of the HUPO Human Proteome Project and of neXtProt. Multiple efforts have catalogued splice isoforms as "dominant", "principal", or "major" isoforms based on expression or evolutionary traits. In contrast, we recently proposed Highest Connected Isoforms (HCIs) as a new class of canonical isoforms that have the strongest interactions in a functional network and revealed their significantly higher (differential) transcript-level expression compared to Non-highest Connected isoforms (NCIs) regardless of tissues/cell lines in the mouse. HCIs and their expression behavior in the human remain unexplored. Here we identified HCIs for 6157 multi-isoform genes using a human isoform network that we constructed by integrating a large compendium of heterogeneous genomic data. We present examples for pairs of transcript isoforms of ABCC3, RBM34, ERBB2 and ANXA7. We found that functional networks of isoforms of the same gene can show large differences. Interestingly, differential expression between HCIs and NCIs was also observed in the human on an independent set of 940 RNA-seq samples across multiple tissues, including heart, kidney and liver. Using proteomic data from normal human retina and placenta, we showed that HCIs are a promising indicator of expressed protein isoforms exemplified by NUDFB6 and M6PR. Furthermore, we found that a significant percentage (20%, p=0.0003) of human and mouse HCIs are homologs, suggesting their conservation between species. Our identified HCIs expand the repertoire of canonical isoforms and are expected to facilitate studying main protein products, understanding gene regulation, and possibly evolution. The network is available through our web server as a rich resource for investigating isoform functional relationships (http://guanlab.ccmb.med.umich.edu/hisonet). All MS/MS data were available at ProteomeXchange website (http://www.proteomexchange.org) through their identifiers (retina: PXD001242, placenta: PXD000754).

DOI10.1021/acs.jproteome.5b00494
Alternate JournalJ. Proteome Res.
PubMed ID26216192