Abstract

Epigenetic profile is the link between the regulation of nuclear gene expression and the environment. The most important factors capable of significantly affecting the cellular environment are the amount and quality of nutrients available. Mitochondria are both involved in the production of some of the molecules capable of directly affecting the epigenome and have a critical role in the conversion of nutrients into usable energy. Carbohydrate and fats are converted into ATP, acetyl-CoA, SAM, and NADH. These high-energy substrates are, in turn, capable of driving the epigenetic profile. We describe substances capable of affecting this mechanism. On the other hand, nutritional interventions capable of reducing calories or significantly impairing the normal Acetyl-CoA production or the SAM-SAH ratio also impact chromatin methylation and histone modification, suggesting a critical role of mitochondria on nutrient-dependent epigenetic profile.

Highlights

  • Mitochondrion at the Crossroad Between Nutrients and EpigenomeOncological and Stomatological Disciplines Department, Medical School, University of Palermo, Palermo, Italy

  • The analysis of the non-genetic factors network, capable of affecting the lifespan of living organisms, revealed nutrition as a major determinant of longevity

  • Recent advances suggest that nutrition can affect the epigenome through 2 general mechanisms: either directly, thanks to substances, which interact with the enzymes responsible for “writing” or “erasing” the epigenetic profiles; or indirectly through metabolic rewiring

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Summary

Mitochondrion at the Crossroad Between Nutrients and Epigenome

Oncological and Stomatological Disciplines Department, Medical School, University of Palermo, Palermo, Italy. Specialty section: This article was submitted to Endocrinology of Aging, a section of the journal

Frontiers in Endocrinology
INTRODUCTION
NUTRIENT CAPABLE TO DIRECTLY AFFECT THE EPIGENOME
Nutrient and Epigenome
Effects on mitochondria
NUTRIENTS INDIRECTLY AFFECTING THE EPIGENOME
CONCLUSION
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