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The contributions of normal variation and genetic background to mammalian gene expression

BACKGROUND: Qualitative and quantitative variability in gene expression represents the substrate for external conditions to exert selective pressures for natural selection. Current technologies allow for some forms of genetic variation, such as DNA mutations and polymorphisms, to be determined accur...

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Autores principales: Pritchard, Colin, Coil, David, Hawley, Sarah, Hsu, Li, Nelson, Peter S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557746/
https://www.ncbi.nlm.nih.gov/pubmed/16584536
http://dx.doi.org/10.1186/gb-2006-7-3-r26
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author Pritchard, Colin
Coil, David
Hawley, Sarah
Hsu, Li
Nelson, Peter S
author_facet Pritchard, Colin
Coil, David
Hawley, Sarah
Hsu, Li
Nelson, Peter S
author_sort Pritchard, Colin
collection PubMed
description BACKGROUND: Qualitative and quantitative variability in gene expression represents the substrate for external conditions to exert selective pressures for natural selection. Current technologies allow for some forms of genetic variation, such as DNA mutations and polymorphisms, to be determined accurately on a comprehensive scale. Other components of variability, such as stochastic events in cellular transcriptional and translational processes, are less well characterized. Although potentially important, the relative contributions of genomic versus epigenetic and stochastic factors to variation in gene expression have not been quantified in mammalian species. RESULTS: In this study we compared microarray-based measures of hepatic transcript abundance levels within and between five different strains of Mus musculus. Within each strain 23% to 44% of all genes exhibited statistically significant differences in expression between genetically identical individuals (positive false discovery rate of 10%). Genes functionally associated with cell growth, cytokine activity, amine metabolism, and ubiquitination were enriched in this group. Genetic divergence between individuals of different strains also contributed to transcript abundance level differences, but to a lesser extent than intra-strain variation, with approximately 3% of all genes exhibiting inter-strain expression differences. CONCLUSION: These results indicate that although DNA sequence fixes boundaries for gene expression variability, there remain considerable latitudes of expression within these genome-defined limits that have the potential to influence phenotypes. The extent of normal or expected natural variability in gene expression may provide an additional level of phenotypic opportunity for natural selection.
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spelling pubmed-15577462006-09-01 The contributions of normal variation and genetic background to mammalian gene expression Pritchard, Colin Coil, David Hawley, Sarah Hsu, Li Nelson, Peter S Genome Biol Research BACKGROUND: Qualitative and quantitative variability in gene expression represents the substrate for external conditions to exert selective pressures for natural selection. Current technologies allow for some forms of genetic variation, such as DNA mutations and polymorphisms, to be determined accurately on a comprehensive scale. Other components of variability, such as stochastic events in cellular transcriptional and translational processes, are less well characterized. Although potentially important, the relative contributions of genomic versus epigenetic and stochastic factors to variation in gene expression have not been quantified in mammalian species. RESULTS: In this study we compared microarray-based measures of hepatic transcript abundance levels within and between five different strains of Mus musculus. Within each strain 23% to 44% of all genes exhibited statistically significant differences in expression between genetically identical individuals (positive false discovery rate of 10%). Genes functionally associated with cell growth, cytokine activity, amine metabolism, and ubiquitination were enriched in this group. Genetic divergence between individuals of different strains also contributed to transcript abundance level differences, but to a lesser extent than intra-strain variation, with approximately 3% of all genes exhibiting inter-strain expression differences. CONCLUSION: These results indicate that although DNA sequence fixes boundaries for gene expression variability, there remain considerable latitudes of expression within these genome-defined limits that have the potential to influence phenotypes. The extent of normal or expected natural variability in gene expression may provide an additional level of phenotypic opportunity for natural selection. BioMed Central 2006 2006-03-31 /pmc/articles/PMC1557746/ /pubmed/16584536 http://dx.doi.org/10.1186/gb-2006-7-3-r26 Text en Copyright © 2006 Pritchard et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article ditributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribtion, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Pritchard, Colin
Coil, David
Hawley, Sarah
Hsu, Li
Nelson, Peter S
The contributions of normal variation and genetic background to mammalian gene expression
title The contributions of normal variation and genetic background to mammalian gene expression
title_full The contributions of normal variation and genetic background to mammalian gene expression
title_fullStr The contributions of normal variation and genetic background to mammalian gene expression
title_full_unstemmed The contributions of normal variation and genetic background to mammalian gene expression
title_short The contributions of normal variation and genetic background to mammalian gene expression
title_sort contributions of normal variation and genetic background to mammalian gene expression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557746/
https://www.ncbi.nlm.nih.gov/pubmed/16584536
http://dx.doi.org/10.1186/gb-2006-7-3-r26
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