Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models.
Characterizing the relationships between genomic and phenotypic variation is essential to understanding disease etiology. Information-dense data sets derived from pathophysiological, proteomic and transcriptomic profiling have been applied to map quantitative trait loci (QTLs). Metabolic traits, alr...
| Main Authors: | , , , , , , , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2007
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| _version_ | 1797054571181244416 |
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| author | Dumas, M Wilder, S Bihoreau, M Barton, R Fearnside, J Argoud, K D'Amato, L Wallis, R Blancher, C Keun, H Baunsgaard, D Scott, J Sidelmann, U Nicholson, J Gauguier, D |
| author_facet | Dumas, M Wilder, S Bihoreau, M Barton, R Fearnside, J Argoud, K D'Amato, L Wallis, R Blancher, C Keun, H Baunsgaard, D Scott, J Sidelmann, U Nicholson, J Gauguier, D |
| author_sort | Dumas, M |
| collection | OXFORD |
| description | Characterizing the relationships between genomic and phenotypic variation is essential to understanding disease etiology. Information-dense data sets derived from pathophysiological, proteomic and transcriptomic profiling have been applied to map quantitative trait loci (QTLs). Metabolic traits, already used in QTL studies in plants, are essential phenotypes in mammalian genetics to define disease biomarkers. Using a complex mammalian system, here we show chromosomal mapping of untargeted plasma metabolic fingerprints derived from NMR spectroscopic analysis in a cross between diabetic and control rats. We propose candidate metabolites for the most significant QTLs. Metabolite profiling in congenic strains provided evidence of QTL replication. Linkage to a gut microbial metabolite (benzoate) can be explained by deletion of a uridine diphosphate glucuronosyltransferase. Mapping metabotypic QTLs provides a practical approach to understanding genome-phenotype relationships in mammals and may uncover deeper biological complexity, as extended genome (microbiome) perturbations that affect disease processes through transgenomic effects may influence QTL detection. |
| first_indexed | 2024-03-06T18:59:05Z |
| format | Journal article |
| id | oxford-uuid:12e6bbfd-68bf-4841-a975-e0533f4e38ed |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T18:59:05Z |
| publishDate | 2007 |
| record_format | dspace |
| spelling | oxford-uuid:12e6bbfd-68bf-4841-a975-e0533f4e38ed2022-03-26T10:10:38ZDirect quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:12e6bbfd-68bf-4841-a975-e0533f4e38edEnglishSymplectic Elements at Oxford2007Dumas, MWilder, SBihoreau, MBarton, RFearnside, JArgoud, KD'Amato, LWallis, RBlancher, CKeun, HBaunsgaard, DScott, JSidelmann, UNicholson, JGauguier, DCharacterizing the relationships between genomic and phenotypic variation is essential to understanding disease etiology. Information-dense data sets derived from pathophysiological, proteomic and transcriptomic profiling have been applied to map quantitative trait loci (QTLs). Metabolic traits, already used in QTL studies in plants, are essential phenotypes in mammalian genetics to define disease biomarkers. Using a complex mammalian system, here we show chromosomal mapping of untargeted plasma metabolic fingerprints derived from NMR spectroscopic analysis in a cross between diabetic and control rats. We propose candidate metabolites for the most significant QTLs. Metabolite profiling in congenic strains provided evidence of QTL replication. Linkage to a gut microbial metabolite (benzoate) can be explained by deletion of a uridine diphosphate glucuronosyltransferase. Mapping metabotypic QTLs provides a practical approach to understanding genome-phenotype relationships in mammals and may uncover deeper biological complexity, as extended genome (microbiome) perturbations that affect disease processes through transgenomic effects may influence QTL detection. |
| spellingShingle | Dumas, M Wilder, S Bihoreau, M Barton, R Fearnside, J Argoud, K D'Amato, L Wallis, R Blancher, C Keun, H Baunsgaard, D Scott, J Sidelmann, U Nicholson, J Gauguier, D Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. |
| title | Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. |
| title_full | Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. |
| title_fullStr | Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. |
| title_full_unstemmed | Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. |
| title_short | Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models. |
| title_sort | direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models |
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