[PDF][PDF] Tissue-specific alternative splicing remodels protein-protein interaction networks

JD Ellis, M Barrios-Rodiles, R Colak, M Irimia, TH Kim… - Molecular cell, 2012 - cell.com
JD Ellis, M Barrios-Rodiles, R Colak, M Irimia, TH Kim, JA Calarco, X Wang, Q Pan…
Molecular cell, 2012cell.com
Alternative splicing plays a key role in the expansion of proteomic and regulatory complexity,
yet the functions of the vast majority of differentially spliced exons are not known. In this
study, we observe that brain and other tissue-regulated exons are significantly enriched in
flexible regions of proteins that likely form conserved interaction surfaces. These proteins
participate in significantly more interactions in protein-protein interaction (PPI) networks than
other proteins. Using LUMIER, an automated PPI assay, we observe that approximately one …
Summary
Alternative splicing plays a key role in the expansion of proteomic and regulatory complexity, yet the functions of the vast majority of differentially spliced exons are not known. In this study, we observe that brain and other tissue-regulated exons are significantly enriched in flexible regions of proteins that likely form conserved interaction surfaces. These proteins participate in significantly more interactions in protein-protein interaction (PPI) networks than other proteins. Using LUMIER, an automated PPI assay, we observe that approximately one-third of analyzed neural-regulated exons affect PPIs. Inclusion of these exons stimulated and repressed different partner interactions at comparable frequencies. This assay further revealed functions of individual exons, including a role for a neural-specific exon in promoting an interaction between Bridging Integrator 1 (Bin1)/Amphiphysin II and Dynamin 2 (Dnm2) that facilitates endocytosis. Collectively, our results provide evidence that regulated alternative exons frequently remodel interactions to establish tissue-dependent PPI networks.
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