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  • MITOCH_2019_53_Revision 1_PURE

    Rights statement: This is the author’s version of a work that was accepted for publication in Mitochondrion. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Mitochondrion, 49, 2019 DOI: 10.1016/j.mito.2019.06.009

    Accepted author manuscript, 461 KB, PDF document

    Embargo ends: 26/06/20

    Available under license: CC BY-NC-ND

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Mitonuclear gene X environment effects on lifespan and health: How common, how big?

Research output: Contribution to journalJournal article

E-pub ahead of print
<mark>Journal publication date</mark>1/11/2019
<mark>Journal</mark>Mitochondrion
Volume49
Number of pages7
Pages (from-to)12-18
Publication statusE-pub ahead of print
Early online date26/06/19
Original languageEnglish

Abstract

Mitochondrial genetic variation can have profound effects on fitness, and the mitotype must interact with both the nuclear genes and the environment. We used Drosophila to investigate the extent to which mitotype effects on lifespan and activity are modulated by nucleotype and environmental variation. When nucleotype is varied, mitochondrial effects on lifespan persisted but were relatively small, and still male biased. Varying food as well, mitotype had substantial effects on male climbing speed, modifiable by nucleotype but less so by diet. Finally, mitotype affected fly lifespan much more in a cage environment compared with a vial, also modifiable by nucleotype and diet. The cage may represent a stressful environment. Mitochondrial genotype may affect fitness much more in conditions of stress, which may have implications for human health.

Bibliographic note

This is the author’s version of a work that was accepted for publication in Mitochondrion. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Mitochondrion, 49, 2019 DOI: 10.1016/j.mito.2019.06.009