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Tissue-specific mouse mRNA isoform networks
Alternative Splicing produces multiple mRNA isoforms of genes which have important diverse roles such as regulation of gene expression, human heritable diseases, and response to environmental stresses. However, little has been done to assign functions at the mRNA isoform level. Functional networks,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765046/ https://www.ncbi.nlm.nih.gov/pubmed/31562339 http://dx.doi.org/10.1038/s41598-019-50119-x |
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author | Kandoi, Gaurav Dickerson, Julie A. |
author_facet | Kandoi, Gaurav Dickerson, Julie A. |
author_sort | Kandoi, Gaurav |
collection | PubMed |
description | Alternative Splicing produces multiple mRNA isoforms of genes which have important diverse roles such as regulation of gene expression, human heritable diseases, and response to environmental stresses. However, little has been done to assign functions at the mRNA isoform level. Functional networks, where the interactions are quantified by their probability of being involved in the same biological process are typically generated at the gene level. We use a diverse array of tissue-specific RNA-seq datasets and sequence information to train random forest models that predict the functional networks. Since there is no mRNA isoform-level gold standard, we use single isoform genes co-annotated to Gene Ontology biological process annotations, Kyoto Encyclopedia of Genes and Genomes pathways, BioCyc pathways and protein-protein interactions as functionally related (positive pair). To generate the non-functional pairs (negative pair), we use the Gene Ontology annotations tagged with “NOT” qualifier. We describe 17 Tissue-spEcific mrNa iSoform functIOnal Networks (TENSION) following a leave-one-tissue-out strategy in addition to an organism level reference functional network for mouse. We validate our predictions by comparing its performance with previous methods, randomized positive and negative class labels, updated Gene Ontology annotations, and by literature evidence. We demonstrate the ability of our networks to reveal tissue-specific functional differences of the isoforms of the same genes. All scripts and data from TENSION are available at: 10.25380/iastate.c.4275191. |
format | Online Article Text |
id | pubmed-6765046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67650462019-10-02 Tissue-specific mouse mRNA isoform networks Kandoi, Gaurav Dickerson, Julie A. Sci Rep Article Alternative Splicing produces multiple mRNA isoforms of genes which have important diverse roles such as regulation of gene expression, human heritable diseases, and response to environmental stresses. However, little has been done to assign functions at the mRNA isoform level. Functional networks, where the interactions are quantified by their probability of being involved in the same biological process are typically generated at the gene level. We use a diverse array of tissue-specific RNA-seq datasets and sequence information to train random forest models that predict the functional networks. Since there is no mRNA isoform-level gold standard, we use single isoform genes co-annotated to Gene Ontology biological process annotations, Kyoto Encyclopedia of Genes and Genomes pathways, BioCyc pathways and protein-protein interactions as functionally related (positive pair). To generate the non-functional pairs (negative pair), we use the Gene Ontology annotations tagged with “NOT” qualifier. We describe 17 Tissue-spEcific mrNa iSoform functIOnal Networks (TENSION) following a leave-one-tissue-out strategy in addition to an organism level reference functional network for mouse. We validate our predictions by comparing its performance with previous methods, randomized positive and negative class labels, updated Gene Ontology annotations, and by literature evidence. We demonstrate the ability of our networks to reveal tissue-specific functional differences of the isoforms of the same genes. All scripts and data from TENSION are available at: 10.25380/iastate.c.4275191. Nature Publishing Group UK 2019-09-27 /pmc/articles/PMC6765046/ /pubmed/31562339 http://dx.doi.org/10.1038/s41598-019-50119-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kandoi, Gaurav Dickerson, Julie A. Tissue-specific mouse mRNA isoform networks |
title | Tissue-specific mouse mRNA isoform networks |
title_full | Tissue-specific mouse mRNA isoform networks |
title_fullStr | Tissue-specific mouse mRNA isoform networks |
title_full_unstemmed | Tissue-specific mouse mRNA isoform networks |
title_short | Tissue-specific mouse mRNA isoform networks |
title_sort | tissue-specific mouse mrna isoform networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765046/ https://www.ncbi.nlm.nih.gov/pubmed/31562339 http://dx.doi.org/10.1038/s41598-019-50119-x |
work_keys_str_mv | AT kandoigaurav tissuespecificmousemrnaisoformnetworks AT dickersonjuliea tissuespecificmousemrnaisoformnetworks |