Dual Regulation Mechanism of Obesity: DNA Methylation and Intestinal Flora
- PMID: 39200098
- PMCID: PMC11351752
- DOI: 10.3390/biomedicines12081633
Dual Regulation Mechanism of Obesity: DNA Methylation and Intestinal Flora
Abstract
Obesity is a multifactorial chronic inflammatory metabolic disorder, with pathogenesis influenced by genetic and non-genetic factors such as environment and diet. Intestinal microbes and their metabolites play significant roles in the occurrence and development of obesity by regulating energy metabolism, inducing chronic inflammation, and impacting intestinal hormone secretion. Epigenetics, which involves the regulation of host gene expression without changing the nucleotide sequence, provides an exact direction for us to understand how the environment, lifestyle factors, and other risk factors contribute to obesity. DNA methylation, as the most common epigenetic modification, is involved in the pathogenesis of various metabolic diseases. The epigenetic modification of the host is induced or regulated by the intestinal microbiota and their metabolites, linking the dynamic interaction between the microbiota and the host genome. In this review, we examined recent advancements in research, focusing on the involvement of intestinal microbiota and DNA methylation in the etiology and progression of obesity, as well as potential interactions between the two factors, providing novel perspectives and avenues for further elucidating the pathogenesis, prevention, and treatment of obesity.
Keywords: DNA methylation; epigenetics; intestinal flora; obesity.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures



Similar articles
-
Epigenetic factors in atherosclerosis: DNA methylation, folic acid metabolism, and intestinal microbiota.Clin Chim Acta. 2021 Jan;512:7-11. doi: 10.1016/j.cca.2020.11.013. Epub 2020 Nov 21. Clin Chim Acta. 2021. PMID: 33232735 Review.
-
Epigenetic Markers and Microbiota/Metabolite-Induced Epigenetic Modifications in the Pathogenesis of Obesity, Metabolic Syndrome, Type 2 Diabetes, and Non-alcoholic Fatty Liver Disease.Curr Diab Rep. 2019 May 1;19(6):31. doi: 10.1007/s11892-019-1151-4. Curr Diab Rep. 2019. PMID: 31044315 Free PMC article. Review.
-
The Gut Microbial Regulation of Epigenetic Modification from a Metabolic Perspective.Int J Mol Sci. 2024 Jun 29;25(13):7175. doi: 10.3390/ijms25137175. Int J Mol Sci. 2024. PMID: 39000282 Free PMC article. Review.
-
Bidirectional Mediation Effects between Intratumoral Microbiome and Host DNA Methylation Changes Contribute to Stomach Adenocarcinoma.Microbiol Spectr. 2023 Aug 17;11(4):e0090423. doi: 10.1128/spectrum.00904-23. Epub 2023 Jun 1. Microbiol Spectr. 2023. PMID: 37260411 Free PMC article.
-
Diet, Gut Microbiota, and Obesity: Links with Host Genetics and Epigenetics and Potential Applications.Adv Nutr. 2019 Jan 1;10(suppl_1):S17-S30. doi: 10.1093/advances/nmy078. Adv Nutr. 2019. PMID: 30721960 Free PMC article. Review.
Cited by
-
Molecular Mechanisms Against Successful Weight Loss and Promising Treatment Options in Obesity.Biomedicines. 2025 Aug 15;13(8):1989. doi: 10.3390/biomedicines13081989. Biomedicines. 2025. PMID: 40868241 Free PMC article. Review.
-
Hylocereus polyrhizus Pulp Residues Polysaccharide Alleviates High-Fat Diet-Induced Obesity by Modulating Intestinal Mucus Secretion and Glycosylation.Foods. 2025 Aug 1;14(15):2708. doi: 10.3390/foods14152708. Foods. 2025. PMID: 40807645 Free PMC article.
-
DNA methylation in adaptation to high-altitude environments and pathogenesis of related diseases.Hum Genomics. 2025 Aug 30;19(1):100. doi: 10.1186/s40246-025-00794-x. Hum Genomics. 2025. PMID: 40886024 Free PMC article. Review.
References
-
- World Health Organization Obesity and Overweight–Key Facts. WHO. 2018. [(accessed on 20 May 2024)]. Available online: http://www.who.int/mediacentre/factsheets/fs311/en/
Publication types
Grants and funding
- 2023SK4018/the Science and Technology Program of Hunan Province
- 2024JJ8249/the Science and Technology Program of Hunan Province
- 2024ZZTS0161/the Fundamental Research Funds for the Center Universities of Central South University
- 820MS168/the Hainan Provincial Natural Science Foundation of China
- 822RC871/the Hainan Provincial Natural Science Foundation of China
LinkOut - more resources
Full Text Sources
Molecular Biology Databases