Association between Adherence to a Mediterranean Diet Pattern and DNA Methylation of the Main Autophagy-Related Genes
Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its deregulation has been associated with common cv and brain diseases. In animal models, autophagy activity is regulated by epigenetic mechanisms in respons...
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Published in | Current developments in nutrition Vol. 6; no. Supplement_1; p. 6 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford
Elsevier Inc
01.06.2022
Oxford University Press |
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Abstract | Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its deregulation has been associated with common cv and brain diseases. In animal models, autophagy activity is regulated by epigenetic mechanisms in response to diet. However, very few studies have analyzed the diet-autophagy relationship in humans. Our aim is to study the association between the adherence to the Mediterranean diet (MedDiet) and the DNA-methylation of the main autophagy-related genes.
We have analyzed 410 subjects (aged 65.5 y) with metabolic syndrome from Valencia (Spain) and measured the adherence to the MedDiet by a 17-item score. DNA methylation from leukocytes was analyzed by the Illumina EPIC850K Human array. A comprehensive list (n = 141) of the main autophagy-related genes was selected from the literature. Multivariate adjusted models including potential confounders were fitted and gene-ontology (GO) enrichment was analyzed.
In a model adjusted for sex, age, batch effect, diabetes, body mass index, medications, leukocyte types, smoking and adherence to MedDiet, we found significant associations between MedDiet adherence and the differential methylation of several cpg sites of the selected autophagy-related genes: cg17676428 (top-ranked cpg site) in TOLLIP (Toll interactive protein) gene (p = 9.3 × 10–6). This is a ubiquitin binding protein that regulates innate immune response. Its deficiency alters atherosclerosis and steatosis. The other hits: cg12573747 in HTT (Huntingtin) gene (p = 4.5 × 10–5), a gene related to the DNA protection in neurons; the cg09197074 (p = 7.8 × 10–5) in HSPA8 (Heat shock protein family A (Hsp70) member 8), that functions as a chaperone and protects the proteome from stress. The GO analysis identified as top-ranked enriched functions: autophagosome membrane; organelle disassembly; selective autophagy; vacuole; phagophore assembly; etc.
A higher adherence to the MedDiet is associated with differential DNA-methylation on relevant autophagy related genes and may have a potential effect upregulating autophagy.
Generalitat Valenciana (grant PROMETEO/2021/021). Grant PID2019-108858RB-I00 is funded by AEI 10.13039/501100011033 and, by “ERDF A way of making Europe”. |
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AbstractList | Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its deregulation has been associated with common cv and brain diseases. In animal models, autophagy activity is regulated by epigenetic mechanisms in response to diet. However, very few studies have analyzed the diet-autophagy relationship in humans. Our aim is to study the association between the adherence to the Mediterranean diet (MedDiet) and the DNA-methylation of the main autophagy-related genes.
We have analyzed 410 subjects (aged 65.5 y) with metabolic syndrome from Valencia (Spain) and measured the adherence to the MedDiet by a 17-item score. DNA methylation from leukocytes was analyzed by the Illumina EPIC850K Human array. A comprehensive list (n = 141) of the main autophagy-related genes was selected from the literature. Multivariate adjusted models including potential confounders were fitted and gene-ontology (GO) enrichment was analyzed.
In a model adjusted for sex, age, batch effect, diabetes, body mass index, medications, leukocyte types, smoking and adherence to MedDiet, we found significant associations between MedDiet adherence and the differential methylation of several cpg sites of the selected autophagy-related genes: cg17676428 (top-ranked cpg site) in TOLLIP (Toll interactive protein) gene (p = 9.3 × 10–6). This is a ubiquitin binding protein that regulates innate immune response. Its deficiency alters atherosclerosis and steatosis. The other hits: cg12573747 in HTT (Huntingtin) gene (p = 4.5 × 10–5), a gene related to the DNA protection in neurons; the cg09197074 (p = 7.8 × 10–5) in HSPA8 (Heat shock protein family A (Hsp70) member 8), that functions as a chaperone and protects the proteome from stress. The GO analysis identified as top-ranked enriched functions: autophagosome membrane; organelle disassembly; selective autophagy; vacuole; phagophore assembly; etc.
A higher adherence to the MedDiet is associated with differential DNA-methylation on relevant autophagy related genes and may have a potential effect upregulating autophagy.
Generalitat Valenciana (grant PROMETEO/2021/021). Grant PID2019-108858RB-I00 is funded by AEI 10.13039/501100011033 and, by “ERDF A way of making Europe”. Abstract Objectives Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its deregulation has been associated with common cv and brain diseases. In animal models, autophagy activity is regulated by epigenetic mechanisms in response to diet. However, very few studies have analyzed the diet-autophagy relationship in humans. Our aim is to study the association between the adherence to the Mediterranean diet (MedDiet) and the DNA-methylation of the main autophagy-related genes. Methods We have analyzed 410 subjects (aged 65.5 y) with metabolic syndrome from Valencia (Spain) and measured the adherence to the MedDiet by a 17-item score. DNA methylation from leukocytes was analyzed by the Illumina EPIC850K Human array. A comprehensive list (n = 141) of the main autophagy-related genes was selected from the literature. Multivariate adjusted models including potential confounders were fitted and gene-ontology (GO) enrichment was analyzed. Results In a model adjusted for sex, age, batch effect, diabetes, body mass index, medications, leukocyte types, smoking and adherence to MedDiet, we found significant associations between MedDiet adherence and the differential methylation of several cpg sites of the selected autophagy-related genes: cg17676428 (top-ranked cpg site) in TOLLIP (Toll interactive protein) gene (p = 9.3 × 10–6). This is a ubiquitin binding protein that regulates innate immune response. Its deficiency alters atherosclerosis and steatosis. The other hits: cg12573747 in HTT (Huntingtin) gene (p = 4.5 × 10–5), a gene related to the DNA protection in neurons; the cg09197074 (p = 7.8 × 10–5) in HSPA8 (Heat shock protein family A (Hsp70) member 8), that functions as a chaperone and protects the proteome from stress. The GO analysis identified as top-ranked enriched functions: autophagosome membrane; organelle disassembly; selective autophagy; vacuole; phagophore assembly; etc. Conclusions A higher adherence to the MedDiet is associated with differential DNA-methylation on relevant autophagy related genes and may have a potential effect upregulating autophagy. Funding Sources Generalitat Valenciana (grant PROMETEO/2021/021). Grant PID2019-108858RB-I00 is funded by AEI 10.13039/501100011033 and, by “ERDF A way of making Europe”. Objectives Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its deregulation has been associated with common cv and brain diseases. In animal models, autophagy activity is regulated by epigenetic mechanisms in response to diet. However, very few studies have analyzed the diet-autophagy relationship in humans. Our aim is to study the association between the adherence to the Mediterranean diet (MedDiet) and the DNA-methylation of the main autophagy-related genes. Methods We have analyzed 410 subjects (aged 65.5 y) with metabolic syndrome from Valencia (Spain) and measured the adherence to the MedDiet by a 17-item score. DNA methylation from leukocytes was analyzed by the Illumina EPIC850K Human array. A comprehensive list (n = 141) of the main autophagy-related genes was selected from the literature. Multivariate adjusted models including potential confounders were fitted and gene-ontology (GO) enrichment was analyzed. Results In a model adjusted for sex, age, batch effect, diabetes, body mass index, medications, leukocyte types, smoking and adherence to MedDiet, we found significant associations between MedDiet adherence and the differential methylation of several cpg sites of the selected autophagy-related genes: cg17676428 (top-ranked cpg site) in TOLLIP (Toll interactive protein) gene (p = 9.3 × 10–6). This is a ubiquitin binding protein that regulates innate immune response. Its deficiency alters atherosclerosis and steatosis. The other hits: cg12573747 in HTT (Huntingtin) gene (p = 4.5 × 10–5), a gene related to the DNA protection in neurons; the cg09197074 (p = 7.8 × 10–5) in HSPA8 (Heat shock protein family A (Hsp70) member 8), that functions as a chaperone and protects the proteome from stress. The GO analysis identified as top-ranked enriched functions: autophagosome membrane; organelle disassembly; selective autophagy; vacuole; phagophore assembly; etc. Conclusions A higher adherence to the MedDiet is associated with differential DNA-methylation on relevant autophagy related genes and may have a potential effect upregulating autophagy. Funding Sources Generalitat Valenciana (grant PROMETEO/2021/021). Grant PID2019-108858RB-I00 is funded by AEI 10.13039/501100011033 and, by “ERDF A way of making Europe”. |
Author | Francés, Francesc Sorlí, Jose Coltell, Oscar Guillem-Saiz, Patricia Corella, Dolores Fernández-Carrión, Rebeca Portolés, Olga Saiz, Carmen Barragán, Rocío Castelló-Ponce, Ana |
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Copyright | 2022 American Society for Nutrition. The Author(s) 2022. Published by Oxford University Press on behalf of the American Society for Nutrition. 2022 The Author(s) 2022. Published by Oxford University Press on behalf of the American Society for Nutrition. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Snippet | Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its deregulation... Abstract Objectives Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and... Objectives Autophagy is a dynamic process responsible for protein degradation/recycling as a protective mechanism in response to stress and inflammation. Its... |
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SubjectTerms | Aging and Chronic Disease Autophagy DNA methylation Genes Proteins |
Title | Association between Adherence to a Mediterranean Diet Pattern and DNA Methylation of the Main Autophagy-Related Genes |
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