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Schizophrenia interactome with 504 novel protein–protein interactions

Genome-wide association studies of schizophrenia (GWAS) have revealed the role of rare and common genetic variants, but the functional effects of the risk variants remain to be understood. Protein interactome-based studies can facilitate the study of molecular mechanisms by which the risk genes rela...

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Autores principales: Ganapathiraju, Madhavi K, Thahir, Mohamed, Handen, Adam, Sarkar, Saumendra N, Sweet, Robert A, Nimgaonkar, Vishwajit L, Loscher, Christine E, Bauer, Eileen M, Chaparala, Srilakshmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898894/
https://www.ncbi.nlm.nih.gov/pubmed/27336055
http://dx.doi.org/10.1038/npjschz.2016.12
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author Ganapathiraju, Madhavi K
Thahir, Mohamed
Handen, Adam
Sarkar, Saumendra N
Sweet, Robert A
Nimgaonkar, Vishwajit L
Loscher, Christine E
Bauer, Eileen M
Chaparala, Srilakshmi
author_facet Ganapathiraju, Madhavi K
Thahir, Mohamed
Handen, Adam
Sarkar, Saumendra N
Sweet, Robert A
Nimgaonkar, Vishwajit L
Loscher, Christine E
Bauer, Eileen M
Chaparala, Srilakshmi
author_sort Ganapathiraju, Madhavi K
collection PubMed
description Genome-wide association studies of schizophrenia (GWAS) have revealed the role of rare and common genetic variants, but the functional effects of the risk variants remain to be understood. Protein interactome-based studies can facilitate the study of molecular mechanisms by which the risk genes relate to schizophrenia (SZ) genesis, but protein–protein interactions (PPIs) are unknown for many of the liability genes. We developed a computational model to discover PPIs, which is found to be highly accurate according to computational evaluations and experimental validations of selected PPIs. We present here, 365 novel PPIs of liability genes identified by the SZ Working Group of the Psychiatric Genomics Consortium (PGC). Seventeen genes that had no previously known interactions have 57 novel interactions by our method. Among the new interactors are 19 drug targets that are targeted by 130 drugs. In addition, we computed 147 novel PPIs of 25 candidate genes investigated in the pre-GWAS era. While there is little overlap between the GWAS genes and the pre-GWAS genes, the interactomes reveal that they largely belong to the same pathways, thus reconciling the apparent disparities between the GWAS and prior gene association studies. The interactome including 504 novel PPIs overall, could motivate other systems biology studies and trials with repurposed drugs. The PPIs are made available on a webserver, called Schizo-Pi at http://severus.dbmi.pitt.edu/schizo-pi with advanced search capabilities.
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spelling pubmed-48988942016-06-22 Schizophrenia interactome with 504 novel protein–protein interactions Ganapathiraju, Madhavi K Thahir, Mohamed Handen, Adam Sarkar, Saumendra N Sweet, Robert A Nimgaonkar, Vishwajit L Loscher, Christine E Bauer, Eileen M Chaparala, Srilakshmi NPJ Schizophr Article Genome-wide association studies of schizophrenia (GWAS) have revealed the role of rare and common genetic variants, but the functional effects of the risk variants remain to be understood. Protein interactome-based studies can facilitate the study of molecular mechanisms by which the risk genes relate to schizophrenia (SZ) genesis, but protein–protein interactions (PPIs) are unknown for many of the liability genes. We developed a computational model to discover PPIs, which is found to be highly accurate according to computational evaluations and experimental validations of selected PPIs. We present here, 365 novel PPIs of liability genes identified by the SZ Working Group of the Psychiatric Genomics Consortium (PGC). Seventeen genes that had no previously known interactions have 57 novel interactions by our method. Among the new interactors are 19 drug targets that are targeted by 130 drugs. In addition, we computed 147 novel PPIs of 25 candidate genes investigated in the pre-GWAS era. While there is little overlap between the GWAS genes and the pre-GWAS genes, the interactomes reveal that they largely belong to the same pathways, thus reconciling the apparent disparities between the GWAS and prior gene association studies. The interactome including 504 novel PPIs overall, could motivate other systems biology studies and trials with repurposed drugs. The PPIs are made available on a webserver, called Schizo-Pi at http://severus.dbmi.pitt.edu/schizo-pi with advanced search capabilities. Nature Publishing Group 2016-04-27 /pmc/articles/PMC4898894/ /pubmed/27336055 http://dx.doi.org/10.1038/npjschz.2016.12 Text en Copyright © 2016 Schizophrenia International Research Society/Nature Publishing Group http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ganapathiraju, Madhavi K
Thahir, Mohamed
Handen, Adam
Sarkar, Saumendra N
Sweet, Robert A
Nimgaonkar, Vishwajit L
Loscher, Christine E
Bauer, Eileen M
Chaparala, Srilakshmi
Schizophrenia interactome with 504 novel protein–protein interactions
title Schizophrenia interactome with 504 novel protein–protein interactions
title_full Schizophrenia interactome with 504 novel protein–protein interactions
title_fullStr Schizophrenia interactome with 504 novel protein–protein interactions
title_full_unstemmed Schizophrenia interactome with 504 novel protein–protein interactions
title_short Schizophrenia interactome with 504 novel protein–protein interactions
title_sort schizophrenia interactome with 504 novel protein–protein interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898894/
https://www.ncbi.nlm.nih.gov/pubmed/27336055
http://dx.doi.org/10.1038/npjschz.2016.12
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