Gene-diet interactions associated with complex trait variation in an advanced intercross outbred mouse line
Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of gene-environment interactions on phenotypic traits mostly remains elusive. To address this, we feed 1154 mice of an autoimmunity-prone intercros...
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Published in | Nature communications Vol. 10; no. 1; pp. 4097 - 15 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
10.09.2019
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
ISSN | 2041-1723 2041-1723 |
DOI | 10.1038/s41467-019-11952-w |
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Abstract | Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of gene-environment interactions on phenotypic traits mostly remains elusive. To address this, we feed 1154 mice of an autoimmunity-prone intercross line (AIL) three different diets. We find that diet substantially contributes to the variability of complex traits and unmasks additional genetic susceptibility quantitative trait loci (QTL). By performing whole-genome sequencing of the AIL founder strains, we resolve these QTLs to few or single candidate genes. To address whether diet can also modulate genetic predisposition towards a given trait, we set NZM2410/J mice on similar dietary regimens as AIL mice. Our data suggest that diet modifies genetic susceptibility to lupus and shifts intestinal bacterial and fungal community composition, which precedes clinical disease manifestation. Collectively, our study underlines the importance of including environmental factors in genetic association studies.
Complex traits associate with genetic variation and environment and their interaction. Here, the authors study the influence of different diets on trait variability in 1154 outbred mice from an advanced intercross line and find gene-diet interactions associated with spontaneous autoimmunity development in these animals. |
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AbstractList | Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of gene-environment interactions on phenotypic traits mostly remains elusive. To address this, we feed 1154 mice of an autoimmunity-prone intercross line (AIL) three different diets. We find that diet substantially contributes to the variability of complex traits and unmasks additional genetic susceptibility quantitative trait loci (QTL). By performing whole-genome sequencing of the AIL founder strains, we resolve these QTLs to few or single candidate genes. To address whether diet can also modulate genetic predisposition towards a given trait, we set NZM2410/J mice on similar dietary regimens as AIL mice. Our data suggest that diet modifies genetic susceptibility to lupus and shifts intestinal bacterial and fungal community composition, which precedes clinical disease manifestation. Collectively, our study underlines the importance of including environmental factors in genetic association studies.
Complex traits associate with genetic variation and environment and their interaction. Here, the authors study the influence of different diets on trait variability in 1154 outbred mice from an advanced intercross line and find gene-diet interactions associated with spontaneous autoimmunity development in these animals. Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of gene-environment interactions on phenotypic traits mostly remains elusive. To address this, we feed 1154 mice of an autoimmunity-prone intercross line (AIL) three different diets. We find that diet substantially contributes to the variability of complex traits and unmasks additional genetic susceptibility quantitative trait loci (QTL). By performing whole-genome sequencing of the AIL founder strains, we resolve these QTLs to few or single candidate genes. To address whether diet can also modulate genetic predisposition towards a given trait, we set NZM2410/J mice on similar dietary regimens as AIL mice. Our data suggest that diet modifies genetic susceptibility to lupus and shifts intestinal bacterial and fungal community composition, which precedes clinical disease manifestation. Collectively, our study underlines the importance of including environmental factors in genetic association studies. Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of gene-environment interactions on phenotypic traits mostly remains elusive. To address this, we feed 1154 mice of an autoimmunity-prone intercross line (AIL) three different diets. We find that diet substantially contributes to the variability of complex traits and unmasks additional genetic susceptibility quantitative trait loci (QTL). By performing whole-genome sequencing of the AIL founder strains, we resolve these QTLs to few or single candidate genes. To address whether diet can also modulate genetic predisposition towards a given trait, we set NZM2410/J mice on similar dietary regimens as AIL mice. Our data suggest that diet modifies genetic susceptibility to lupus and shifts intestinal bacterial and fungal community composition, which precedes clinical disease manifestation. Collectively, our study underlines the importance of including environmental factors in genetic association studies.Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of gene-environment interactions on phenotypic traits mostly remains elusive. To address this, we feed 1154 mice of an autoimmunity-prone intercross line (AIL) three different diets. We find that diet substantially contributes to the variability of complex traits and unmasks additional genetic susceptibility quantitative trait loci (QTL). By performing whole-genome sequencing of the AIL founder strains, we resolve these QTLs to few or single candidate genes. To address whether diet can also modulate genetic predisposition towards a given trait, we set NZM2410/J mice on similar dietary regimens as AIL mice. Our data suggest that diet modifies genetic susceptibility to lupus and shifts intestinal bacterial and fungal community composition, which precedes clinical disease manifestation. Collectively, our study underlines the importance of including environmental factors in genetic association studies. Complex traits associate with genetic variation and environment and their interaction. Here, the authors study the influence of different diets on trait variability in 1154 outbred mice from an advanced intercross line and find gene-diet interactions associated with spontaneous autoimmunity development in these animals. |
ArticleNumber | 4097 |
Author | Möller, Steffen Mayadas, Tanya N. Sina, Christian Ibrahim, Saleh M. Bieber, Katja Koga, Hiroshi Jascholt, Joanna Manz, Rudolf A. Sadik, Christian D. Vorobyev, Artem Körber-Ahrens, Heiko Khil’chenko, Stanislav Boehncke, Wolf-Henning Ehlers, Marc Baines, John F. Ludwig, Ralf J. Steinhaus, Moritz Sezin, Tanya Künzel, Sven Diehl, Sandra Kouki, Phillip Schilf, Paul Gupta, Yask Lara Ernst, Anna Zillikens, Detlef Beltsiou, Foteini Bartsch, Yannic C. Al-Aasam, Hassanin Belheouane, Meriem Nishi, Hiroshi |
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Medicine – sequence: 5 givenname: Yannic C. surname: Bartsch fullname: Bartsch, Yannic C. organization: Laboratories of Immunology and Antibody Glycan Analysis, Institute for Nutritional Medicine, University of Lübeck and University Medical Center Schleswig-Holstein – sequence: 6 givenname: Meriem surname: Belheouane fullname: Belheouane, Meriem organization: Max Planck Institute for Evolutionary Biology, Institute for Experimental Medicine, Kiel University – sequence: 7 givenname: Sven surname: Künzel fullname: Künzel, Sven organization: Max Planck Institute for Evolutionary Biology – sequence: 8 givenname: Christian surname: Sina fullname: Sina, Christian organization: Institute of Nutritional Medicine, Molecular Gastroenterology, University of Lübeck, Ratzeburger Allee 160 – sequence: 9 givenname: Paul surname: Schilf fullname: Schilf, Paul organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 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Lübeck – sequence: 14 givenname: Hassanin orcidid: 0000-0002-9331-648X surname: Al-Aasam fullname: Al-Aasam, Hassanin organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 15 givenname: Rudolf A. orcidid: 0000-0003-1263-7693 surname: Manz fullname: Manz, Rudolf A. organization: Institute for Systemic Inflammation Research, University of Lübeck – sequence: 16 givenname: Sandra surname: Diehl fullname: Diehl, Sandra organization: Department of Dermatology, Venereology and Allergology, Goethe University – sequence: 17 givenname: Moritz surname: Steinhaus fullname: Steinhaus, Moritz organization: Laboratories of Immunology and Antibody Glycan Analysis, Institute for Nutritional Medicine, University of Lübeck and University Medical Center Schleswig-Holstein – sequence: 18 givenname: Joanna surname: Jascholt fullname: Jascholt, Joanna organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 19 givenname: Phillip surname: Kouki fullname: Kouki, Phillip organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 20 givenname: Wolf-Henning surname: Boehncke fullname: Boehncke, Wolf-Henning organization: Divison of Dermatology and Venereology, Geneva University Hospitals, and Department of Pathology and Immunology, University of Geneva – sequence: 21 givenname: Tanya N. surname: Mayadas fullname: Mayadas, Tanya N. organization: Center for Excellence in Vascular Biology, Department of Pathology, Brigham and Women’s Hospital and Harvard Medical School – sequence: 22 givenname: Detlef orcidid: 0000-0002-5668-307X surname: Zillikens fullname: Zillikens, Detlef organization: Department of Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 23 givenname: Christian D. orcidid: 0000-0001-6701-048X surname: Sadik fullname: Sadik, Christian D. organization: Department of Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 24 givenname: Hiroshi surname: Nishi fullname: Nishi, Hiroshi organization: Center for Excellence in Vascular Biology, Department of Pathology, Brigham and Women’s Hospital and Harvard Medical School, Department of Nephrology and Endocrinology, University of Tokyo – sequence: 25 givenname: Marc orcidid: 0000-0002-5383-8603 surname: Ehlers fullname: Ehlers, Marc organization: Laboratories of Immunology and Antibody Glycan Analysis, Institute for Nutritional Medicine, University of Lübeck and University Medical Center Schleswig-Holstein – sequence: 26 givenname: Steffen orcidid: 0000-0002-7187-4683 surname: Möller fullname: Möller, Steffen organization: Institute for Biostatistics and Informatics in Medicine and Ageing Research – sequence: 27 givenname: Katja orcidid: 0000-0002-3855-6683 surname: Bieber fullname: Bieber, Katja organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 28 givenname: John F. surname: Baines fullname: Baines, John F. organization: Max Planck Institute for Evolutionary Biology, Institute for Experimental Medicine, Kiel University – sequence: 29 givenname: Saleh M. surname: Ibrahim fullname: Ibrahim, Saleh M. organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck – sequence: 30 givenname: Ralf J. orcidid: 0000-0002-1394-1737 surname: Ludwig fullname: Ludwig, Ralf J. email: ralf.ludwig@uksh.de organization: Lübeck Institute of Experimental Dermatology and Center for Research on Inflammation of the Skin, University of Lübeck |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31506438$$D View this record in MEDLINE/PubMed |
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Publisher | Nature Publishing Group UK Nature Publishing Group Nature Portfolio |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group – name: Nature Portfolio |
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Snippet | Phenotypic variation of quantitative traits is orchestrated by a complex interplay between the environment (e.g. diet) and genetics. However, the impact of... Complex traits associate with genetic variation and environment and their interaction. Here, the authors study the influence of different diets on trait... |
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SubjectTerms | 38/23 38/91 45 631/208/205 631/208/729/743 631/250/38 64/60 692/308/2056 Animals Animals, Outbred Strains Antibodies, Antinuclear - genetics Autoimmunity Bacteria - growth & development Biodiversity Community composition Crosses, Genetic Diet Environmental factors Environmental impact Female Fungi - growth & development Gene mapping Gene sequencing Genes Genetic Association Studies Genetic Predisposition to Disease Genetics Genomes Genotype-environment interactions Humanities and Social Sciences Intestine Lupus Nephritis - genetics Lupus Nephritis - immunology Male Mice Microbiota multidisciplinary Phenotypic variations Physical Chromosome Mapping Quantitative trait loci Quantitative Trait Loci - genetics Quantitative Trait, Heritable Science Science (multidisciplinary) Spleen - metabolism Transcriptome - genetics Whole Genome Sequencing |
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Title | Gene-diet interactions associated with complex trait variation in an advanced intercross outbred mouse line |
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