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Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression

BACKGROUND: Rapid response to selection was previously observed in mice selected for high levels of inter-male aggression based on number of attacks displayed in a novel social interaction test after isolation housing. Attack levels in this high aggression line (NC900) increased significantly within...

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Autores principales: Nehrenberg, Derrick L, Wang, Shiliang, Buus, Ryan J, Perkins, James, de Villena, Fernando Pardo-Manuel, Pomp, Daniel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022667/
https://www.ncbi.nlm.nih.gov/pubmed/21194443
http://dx.doi.org/10.1186/1471-2156-11-113
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author Nehrenberg, Derrick L
Wang, Shiliang
Buus, Ryan J
Perkins, James
de Villena, Fernando Pardo-Manuel
Pomp, Daniel
author_facet Nehrenberg, Derrick L
Wang, Shiliang
Buus, Ryan J
Perkins, James
de Villena, Fernando Pardo-Manuel
Pomp, Daniel
author_sort Nehrenberg, Derrick L
collection PubMed
description BACKGROUND: Rapid response to selection was previously observed in mice selected for high levels of inter-male aggression based on number of attacks displayed in a novel social interaction test after isolation housing. Attack levels in this high aggression line (NC900) increased significantly within just four generations of selective breeding, suggesting the presence of a locus with large effect. We conducted an experiment using a small (n ≈ 100) F(2 )cross between the ICR-derived, non-inbred NC900 strain and the low aggression inbred strain C57BL/6J, genotyped for 154 fully informative SNPs, to determine if a locus with large effect controls the high-aggression selection trait. A second goal was to use high density SNP genotyping (n = 549,000) in the parental strains to characterize residual patterns of heterozygosity within NC900, and evaluate regions that are identical by descent (IBD) between NC900 and C57BL/6J, to determine what impacts these may have on accuracy and resolution of quantitative trait locus (QTL) mapping in the F(2 )cross. RESULTS: No evidence for a locus with major effect on aggressive behavior in mice was identified. However, several QTL with genomewide significance were mapped for aggression on chromosomes 7 and 19 and other social behavior traits on chromosomes 4, 7, 14, and 19. High density genotyping revealed that 28% of the genome is still segregating among the six NC900 females used to originate the F(2 )cross, and that segregating regions are present on every chromosome but are of widely different sizes. Regions of IBD between NC900 and C57BL/6J are found on every chromosome but are most prominent on chromosomes 10, 16 and X. No significant differences were found for amounts of heterozygosity or prevalence of IBD in QTL regions relative to global analysis. CONCLUSIONS: While no major gene was identified to explain the rapid selection response in the NC900 line, transgressive variation (i.e. where the allele from the C57BL/6J increased attack levels) and a significant role for dominant gene action were hallmarks of the genetic architecture for aggressive behavior uncovered in this study. The high levels of heterozygosity and the distribution of minor allele frequency observed in the NC900 population suggest that maintenance of heterozygosity may have been under selection in this line.
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spelling pubmed-30226672011-01-19 Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression Nehrenberg, Derrick L Wang, Shiliang Buus, Ryan J Perkins, James de Villena, Fernando Pardo-Manuel Pomp, Daniel BMC Genet Research Article BACKGROUND: Rapid response to selection was previously observed in mice selected for high levels of inter-male aggression based on number of attacks displayed in a novel social interaction test after isolation housing. Attack levels in this high aggression line (NC900) increased significantly within just four generations of selective breeding, suggesting the presence of a locus with large effect. We conducted an experiment using a small (n ≈ 100) F(2 )cross between the ICR-derived, non-inbred NC900 strain and the low aggression inbred strain C57BL/6J, genotyped for 154 fully informative SNPs, to determine if a locus with large effect controls the high-aggression selection trait. A second goal was to use high density SNP genotyping (n = 549,000) in the parental strains to characterize residual patterns of heterozygosity within NC900, and evaluate regions that are identical by descent (IBD) between NC900 and C57BL/6J, to determine what impacts these may have on accuracy and resolution of quantitative trait locus (QTL) mapping in the F(2 )cross. RESULTS: No evidence for a locus with major effect on aggressive behavior in mice was identified. However, several QTL with genomewide significance were mapped for aggression on chromosomes 7 and 19 and other social behavior traits on chromosomes 4, 7, 14, and 19. High density genotyping revealed that 28% of the genome is still segregating among the six NC900 females used to originate the F(2 )cross, and that segregating regions are present on every chromosome but are of widely different sizes. Regions of IBD between NC900 and C57BL/6J are found on every chromosome but are most prominent on chromosomes 10, 16 and X. No significant differences were found for amounts of heterozygosity or prevalence of IBD in QTL regions relative to global analysis. CONCLUSIONS: While no major gene was identified to explain the rapid selection response in the NC900 line, transgressive variation (i.e. where the allele from the C57BL/6J increased attack levels) and a significant role for dominant gene action were hallmarks of the genetic architecture for aggressive behavior uncovered in this study. The high levels of heterozygosity and the distribution of minor allele frequency observed in the NC900 population suggest that maintenance of heterozygosity may have been under selection in this line. BioMed Central 2010-12-31 /pmc/articles/PMC3022667/ /pubmed/21194443 http://dx.doi.org/10.1186/1471-2156-11-113 Text en Copyright ©2010 Nehrenberg et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nehrenberg, Derrick L
Wang, Shiliang
Buus, Ryan J
Perkins, James
de Villena, Fernando Pardo-Manuel
Pomp, Daniel
Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression
title Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression
title_full Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression
title_fullStr Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression
title_full_unstemmed Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression
title_short Genomic mapping of social behavior traits in a F2 cross derived from mice selectively bred for high aggression
title_sort genomic mapping of social behavior traits in a f2 cross derived from mice selectively bred for high aggression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022667/
https://www.ncbi.nlm.nih.gov/pubmed/21194443
http://dx.doi.org/10.1186/1471-2156-11-113
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