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QTL/microarray approach using pathway information

BACKGROUND: A combined quantitative trait loci (QTL) and microarray-based approach is commonly used to find differentially expressed genes which are then identified based on the known function of a gene in the biological process governing the trait of interest. However, a low cutoff value in individ...

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Autores principales: Matsuda, Hirokazu, Taniguchi, Yukio, Iwaisaki, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340326/
https://www.ncbi.nlm.nih.gov/pubmed/22244197
http://dx.doi.org/10.1186/1748-7188-7-1
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author Matsuda, Hirokazu
Taniguchi, Yukio
Iwaisaki, Hiroaki
author_facet Matsuda, Hirokazu
Taniguchi, Yukio
Iwaisaki, Hiroaki
author_sort Matsuda, Hirokazu
collection PubMed
description BACKGROUND: A combined quantitative trait loci (QTL) and microarray-based approach is commonly used to find differentially expressed genes which are then identified based on the known function of a gene in the biological process governing the trait of interest. However, a low cutoff value in individual gene analyses may result in many genes with moderate but meaningful changes in expression being missed. RESULTS: We modified a gene set analysis to identify intersection sets with significantly affected expression for which the changes in the individual gene sets are less significant. The gene expression profiles in liver tissues of four strains of mice from publicly available microarray sources were analyzed to detect trait-associated pathways using information on the QTL regions of blood concentrations of high density lipoproteins (HDL) cholesterol and insulin-like growth factor 1 (IGF-1). Several metabolic pathways related to HDL levels, including lipid metabolism, ABC transporters and cytochrome P450 pathways were detected for HDL QTL regions. Most of the pathways identified for the IGF-1 phenotype were signal transduction pathways associated with biological processes for IGF-1's regulation. CONCLUSION: We have developed a method of identifying pathways associated with a quantitative trait using information on QTL. Our approach provides insights into genotype-phenotype relations at the level of biological pathways which may help to elucidate the genetic architecture underlying variation in phenotypic traits.
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spelling pubmed-33403262012-05-01 QTL/microarray approach using pathway information Matsuda, Hirokazu Taniguchi, Yukio Iwaisaki, Hiroaki Algorithms Mol Biol Research BACKGROUND: A combined quantitative trait loci (QTL) and microarray-based approach is commonly used to find differentially expressed genes which are then identified based on the known function of a gene in the biological process governing the trait of interest. However, a low cutoff value in individual gene analyses may result in many genes with moderate but meaningful changes in expression being missed. RESULTS: We modified a gene set analysis to identify intersection sets with significantly affected expression for which the changes in the individual gene sets are less significant. The gene expression profiles in liver tissues of four strains of mice from publicly available microarray sources were analyzed to detect trait-associated pathways using information on the QTL regions of blood concentrations of high density lipoproteins (HDL) cholesterol and insulin-like growth factor 1 (IGF-1). Several metabolic pathways related to HDL levels, including lipid metabolism, ABC transporters and cytochrome P450 pathways were detected for HDL QTL regions. Most of the pathways identified for the IGF-1 phenotype were signal transduction pathways associated with biological processes for IGF-1's regulation. CONCLUSION: We have developed a method of identifying pathways associated with a quantitative trait using information on QTL. Our approach provides insights into genotype-phenotype relations at the level of biological pathways which may help to elucidate the genetic architecture underlying variation in phenotypic traits. BioMed Central 2012-01-15 /pmc/articles/PMC3340326/ /pubmed/22244197 http://dx.doi.org/10.1186/1748-7188-7-1 Text en Copyright ©2012 Matsuda et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Matsuda, Hirokazu
Taniguchi, Yukio
Iwaisaki, Hiroaki
QTL/microarray approach using pathway information
title QTL/microarray approach using pathway information
title_full QTL/microarray approach using pathway information
title_fullStr QTL/microarray approach using pathway information
title_full_unstemmed QTL/microarray approach using pathway information
title_short QTL/microarray approach using pathway information
title_sort qtl/microarray approach using pathway information
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340326/
https://www.ncbi.nlm.nih.gov/pubmed/22244197
http://dx.doi.org/10.1186/1748-7188-7-1
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