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Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice

PURPOSE: In a previous study, several quantitative trait loci (QTL) that influence age-related degeneration (ageRD) were identified in a cross between the albino strains B6(Cg)-Tyr(c-2J)/J (B6a) and BALB/cByJ (C). The Chromosome (Chr) 6 and Chr 10 QTL were the strongest and most highly significant l...

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Autores principales: Ogando, Diego G., Dahlquist, Kam D., Alizadeh, Mitra, Kunchithapautham, Kannan, Li, Jun, Yu, Nicole, LaVail, Matthew M., Rohrer, Bärbel, Vollrath, Douglas, Danciger, Michael
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890552/
https://www.ncbi.nlm.nih.gov/pubmed/20577653
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author Ogando, Diego G.
Dahlquist, Kam D.
Alizadeh, Mitra
Kunchithapautham, Kannan
Li, Jun
Yu, Nicole
LaVail, Matthew M.
Rohrer, Bärbel
Vollrath, Douglas
Danciger, Michael
author_facet Ogando, Diego G.
Dahlquist, Kam D.
Alizadeh, Mitra
Kunchithapautham, Kannan
Li, Jun
Yu, Nicole
LaVail, Matthew M.
Rohrer, Bärbel
Vollrath, Douglas
Danciger, Michael
author_sort Ogando, Diego G.
collection PubMed
description PURPOSE: In a previous study, several quantitative trait loci (QTL) that influence age-related degeneration (ageRD) were identified in a cross between the albino strains B6(Cg)-Tyr(c-2J)/J (B6a) and BALB/cByJ (C). The Chromosome (Chr) 6 and Chr 10 QTL were the strongest and most highly significant loci and both involved B6a protective alleles. The QTL were responsible for 21% and 9% of the variance in phenotypes, respectively. We focused on these two QTL to identify candidate genes. METHODS: DNA microarrays were used for the two mouse strains at four and eight months of age to identify genes that are differentially regulated and map to either QTL. Gene Ontology (GO) analysis of the differentially expressed genes was performed to identify possible processes and pathways associated with ageRD. To identify additional candidates, database analyses (Positional Medline or PosMed) were used. Based on differential expression, PosMed, and the presence of reported polymorphisms, five genes per QTL were selected for further study by sequencing analysis and qRT–PCR. Tumor necrosis factor, alpha- induced protein 3 (Tnfaip3; on a C57BL/6J (B6) background) was phenotypically tested. Single nucleotide polymorphisms (SNPs) flanking this gene were correlated with outer nuclear layer thickness (ONL), and eight-month-old Tnfaip3(+/−) mice were tested for ageRD. RESULTS: Polymorphisms were found in the coding regions of eight genes. Changes in gene expression were identified by qRT–PCR for Hexokinase 2 (Hk2) and Docking protein 1 (Dok1) at four months and for Dok1 and Tnfaip3 at eight months. Tnfaip3 was selected for phenotypic testing due to differential expression and the presence of two nonsynonymous mutations. However, when ONL thickness was compared in eight-month-old congenic Tnfaip3(+/−) and Tnfaip3(+/+) mice, no differences were found, suggesting that Tnfaip3 is not the quantitative trait gene (QTG) for the Chr 10 QTL. The GO analysis revealed that GO terms associated with stress and cell remodeling are overrepresented in the ageRD-sensitive C strain compared with the B6a strain with age (eight months). In the ageRD-resistant B6a strain, compared with the C strain, GO terms associated with antioxidant response and the regulation of blood vessel size are overrepresented with age. CONCLUSIONS: The analyses of differentially expressed genes and the PosMed database yielded candidate genes for the Chr 6 and Chr 10 QTL. HtrA serine peptidase 2 (Htra2), Dok1, and Tnfaip3 were deemed most promising because of their known roles in apoptosis and our finding of nonsynonymous substitutions between B6a and C strains. While Tnfaip3 was excluded as the QTG for the Chr 10 QTL, Dok1 and Htra2 remain good candidates for the Chr 6 QTL. Finally, the GO term analysis further supports the general hypothesis that oxidative stress is involved in ageRD.
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spelling pubmed-28905522010-06-24 Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice Ogando, Diego G. Dahlquist, Kam D. Alizadeh, Mitra Kunchithapautham, Kannan Li, Jun Yu, Nicole LaVail, Matthew M. Rohrer, Bärbel Vollrath, Douglas Danciger, Michael Mol Vis Research Article PURPOSE: In a previous study, several quantitative trait loci (QTL) that influence age-related degeneration (ageRD) were identified in a cross between the albino strains B6(Cg)-Tyr(c-2J)/J (B6a) and BALB/cByJ (C). The Chromosome (Chr) 6 and Chr 10 QTL were the strongest and most highly significant loci and both involved B6a protective alleles. The QTL were responsible for 21% and 9% of the variance in phenotypes, respectively. We focused on these two QTL to identify candidate genes. METHODS: DNA microarrays were used for the two mouse strains at four and eight months of age to identify genes that are differentially regulated and map to either QTL. Gene Ontology (GO) analysis of the differentially expressed genes was performed to identify possible processes and pathways associated with ageRD. To identify additional candidates, database analyses (Positional Medline or PosMed) were used. Based on differential expression, PosMed, and the presence of reported polymorphisms, five genes per QTL were selected for further study by sequencing analysis and qRT–PCR. Tumor necrosis factor, alpha- induced protein 3 (Tnfaip3; on a C57BL/6J (B6) background) was phenotypically tested. Single nucleotide polymorphisms (SNPs) flanking this gene were correlated with outer nuclear layer thickness (ONL), and eight-month-old Tnfaip3(+/−) mice were tested for ageRD. RESULTS: Polymorphisms were found in the coding regions of eight genes. Changes in gene expression were identified by qRT–PCR for Hexokinase 2 (Hk2) and Docking protein 1 (Dok1) at four months and for Dok1 and Tnfaip3 at eight months. Tnfaip3 was selected for phenotypic testing due to differential expression and the presence of two nonsynonymous mutations. However, when ONL thickness was compared in eight-month-old congenic Tnfaip3(+/−) and Tnfaip3(+/+) mice, no differences were found, suggesting that Tnfaip3 is not the quantitative trait gene (QTG) for the Chr 10 QTL. The GO analysis revealed that GO terms associated with stress and cell remodeling are overrepresented in the ageRD-sensitive C strain compared with the B6a strain with age (eight months). In the ageRD-resistant B6a strain, compared with the C strain, GO terms associated with antioxidant response and the regulation of blood vessel size are overrepresented with age. CONCLUSIONS: The analyses of differentially expressed genes and the PosMed database yielded candidate genes for the Chr 6 and Chr 10 QTL. HtrA serine peptidase 2 (Htra2), Dok1, and Tnfaip3 were deemed most promising because of their known roles in apoptosis and our finding of nonsynonymous substitutions between B6a and C strains. While Tnfaip3 was excluded as the QTG for the Chr 10 QTL, Dok1 and Htra2 remain good candidates for the Chr 6 QTL. Finally, the GO term analysis further supports the general hypothesis that oxidative stress is involved in ageRD. Molecular Vision 2010-06-05 /pmc/articles/PMC2890552/ /pubmed/20577653 Text en Copyright © 2010 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ogando, Diego G.
Dahlquist, Kam D.
Alizadeh, Mitra
Kunchithapautham, Kannan
Li, Jun
Yu, Nicole
LaVail, Matthew M.
Rohrer, Bärbel
Vollrath, Douglas
Danciger, Michael
Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
title Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
title_full Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
title_fullStr Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
title_full_unstemmed Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
title_short Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
title_sort candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890552/
https://www.ncbi.nlm.nih.gov/pubmed/20577653
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