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Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans.

Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Research Abstract Details 

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  • Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Abstract Text:

    j william o ballardJ William O Ballard,richard g melvinRichard G Melvin,subhash d katewaSubhash D Katewa,koen maasKoen Maas,

    Recent studies have used a variety of theoretical arguments to show that mitochondrial (mt) DNA rarely evolves as a strictly neutral marker and that selection operates on the mtDNA of many species. However, the vast majority of researchers are not convinced by these arguments because data linking mtDNA variation with phenotypic differences are limited. We investigated sequence variation in the three mtDNA and nine nuclear genes (including all isoforms) that encode the 12 subunits of cytochrome c oxidase of the electron transport chain in Drosophila. We then studied cytochrome c oxidase activity as a key aspect of mitochondrial bioenergetics and four life-history traits. In Drosophila simulans, sequence data from the three mtDNA encoded cytochrome c oxidase genes show that there are 76 synonymous and two nonsynonymous fixed differences among flies harboring siII compared with siIII mtDNA. In contrast, 13 nuclear encoded genes show no evidence of genetic subdivision associated with the mtDNA. Flies with siIII mtDNA had higher cytochrome c oxidase activity and were more starvation resistant. Flies harboring siII mtDNA had greater egg size and fecundity, and recovered faster from cold coma. These data are consistent with a causative role for mtDNA variation in these phenotypic differences, but we cannot completely rule out the involvement of nuclear genes. The results of this study have significant implications for the use of mtDNA as an assumed neutral marker and show that evolutionary shifts can involve changes in mtDNA despite the small number of genes encoded in the organelle genome.

    Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Publishing Authors By Initials

    jw ballardJW Ballard,rg melvinRG Melvin,sd katewaSD Katewa,k maasK Maas,

    For similar urogenital system: genitalia: germ cells: ovum research abstracts see: urogenital system: genitalia: germ cells: ovum research

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    Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Evolution; international journal of organic evolut

    VOLUME: 61

    Page Numbers: 1735-47

    Journal Abbreviation: Evolution

    ISSN: 0014-3820

    DAY: 3

    MONTH: Jul

    YEAR: 2007

    Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 373224

    Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Keywords Mesh Terms:

    KEYWORDS: Ovum

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans. Information

    Substance Name: Electron Transport Complex IV

    Registry Number: EC 1.9.3.1

    Grant and Affiliation Information for Mitochondrial DNA variation is associated with measurable differences in life-history traits and mitochondrial metabolism in Drosophila simulans.

    AFFILIATION: Ramaciotti Centre for Gene Function Analysis, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney 2052, Australia. w.ballard@unsw.edu.au

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: R01 GM067862-01

    ACRONYM: GM

    MEDLINETA: Evolution Int J Org Evolution

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