Review: can diet influence the selective advantage of mitochondrial DNA haplotypes?

Biosci Rep. 2015 Nov 5;35(6):e00277. doi: 10.1042/BSR20150232.

Abstract

This review explores the potential for changes in dietary macronutrients to differentially influence mitochondrial bioenergetics and thereby the frequency of mtDNA haplotypes in natural populations. Such dietary modification may be seasonal or result from biogeographic or demographic shifts. Mechanistically, mtDNA haplotypes may influence the activity of the electron transport system (ETS), retrograde signalling to the nuclear genome and affect epigenetic modifications. Thus, differential provisioning by macronutrients may lead to selection through changes in the levels of ATP production, modulation of metabolites (including AMP, reactive oxygen species (ROS) and the NAD(+)/NADH ratio) and potentially complex epigenetic effects. The exquisite complexity of dietary influence on haplotype frequency is further illustrated by the fact that macronutrients may differentially influence the selective advantage of specific mutations in different life-history stages. In Drosophila, complex I mutations may affect larval growth because dietary nutrients are fed through this complex in immaturity. In contrast, the majority of electrons are provided to complex III in adult flies. We conclude the review with a case study that considers specific interactions between diet and complex I of the ETS. Complex I is the first enzyme of the mitochondrial ETS and co-ordinates in the oxidation of NADH and transfer of electrons to ubiquinone. Although the supposition that mtDNA variants may be selected upon by dietary macronutrients could be intuitively consistent to some and counter intuitive to others, it must face a multitude of scientific hurdles before it can be recognized.

Keywords: diet; epigenetics; flavin-adenine dinucleotide (FAD); mitochondria; retrograde response; selection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • DNA, Mitochondrial / genetics*
  • Diet*
  • Drosophila / genetics*
  • Drosophila / metabolism
  • Electron Transport Complex I / genetics
  • Energy Metabolism / genetics
  • Haplotypes / genetics*
  • Oxidative Phosphorylation
  • Reactive Oxygen Species / metabolism
  • Ubiquinone / genetics

Substances

  • DNA, Mitochondrial
  • Reactive Oxygen Species
  • Ubiquinone
  • Electron Transport Complex I