A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>

<p>Abstract</p> <p>Background</p> <p>Mitochondrial DNA (mtDNA) mutations are of increasing interest due to their involvement in aging, disease, fertility, and their role in the evolution of the mitochondrial genome. The presence of reactive oxygen species and the near l...

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Main Authors: Chin Kara, Deshommes Cleonique, Gonzalez-Serricchio Aidyl S, Liau Wei-Siang, LaMunyon Craig W
Format: Article
Language:English
Published: BMC 2007-03-01
Series:BMC Genetics
Online Access:http://www.biomedcentral.com/1471-2156/8/8
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spelling doaj-9eeacf08ac694e538e2d8909b6655b5a2020-11-25T03:07:18ZengBMCBMC Genetics1471-21562007-03-0181810.1186/1471-2156-8-8A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>Chin KaraDeshommes CleoniqueGonzalez-Serricchio Aidyl SLiau Wei-SiangLaMunyon Craig W<p>Abstract</p> <p>Background</p> <p>Mitochondrial DNA (mtDNA) mutations are of increasing interest due to their involvement in aging, disease, fertility, and their role in the evolution of the mitochondrial genome. The presence of reactive oxygen species and the near lack of repair mechanisms cause mtDNA to mutate at a faster rate than nuclear DNA, and mtDNA deletions are not uncommon in the tissues of individuals, although germ-line mtDNA is largely lesion-free. Large-scale deletions in mtDNA may disrupt multiple genes, and curiously, some large-scale deletions persist over many generations in a heteroplasmic state. Here we examine the phenotypic effects of one such deletion, <it>uaDf5</it>, in <it>Caenorhabditis elegans </it>(<it>C. elegans</it>). Our study investigates the phenotypic effects of this 3 kbp deletion.</p> <p>Results</p> <p>The proportion of <it>uaDf5 </it>chromosomes in worms was highly heritable, although <it>uaDf5 </it>content varied from worm to worm and within tissues of individual worms. We also found an impact of the <it>uaDf5 </it>deletion on metabolism. The deletion significantly reduced egg laying rate, defecation rate, and lifespan. Examination of sperm bearing the <it>uaDf5 </it>deletion revealed that sperm crawled more slowly, both in <it>vitro </it>and <it>in vivo</it>.</p> <p>Conclusion</p> <p>Worms harboring <it>uaDf5 </it>are at a selective disadvantage compared to worms with wild-type mtDNA. These effects should lead to the rapid extinction of the deleted chromosome, but it persists indefinitely. We discuss both the implications of this phenomenon and the possible causes of a shortened lifespan for <it>uaDf5 </it>mutant worms.</p> http://www.biomedcentral.com/1471-2156/8/8
collection DOAJ
language English
format Article
sources DOAJ
author Chin Kara
Deshommes Cleonique
Gonzalez-Serricchio Aidyl S
Liau Wei-Siang
LaMunyon Craig W
spellingShingle Chin Kara
Deshommes Cleonique
Gonzalez-Serricchio Aidyl S
Liau Wei-Siang
LaMunyon Craig W
A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>
BMC Genetics
author_facet Chin Kara
Deshommes Cleonique
Gonzalez-Serricchio Aidyl S
Liau Wei-Siang
LaMunyon Craig W
author_sort Chin Kara
title A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>
title_short A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>
title_full A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>
title_fullStr A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>
title_full_unstemmed A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>C. elegans</it>
title_sort persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of <it>c. elegans</it>
publisher BMC
series BMC Genetics
issn 1471-2156
publishDate 2007-03-01
description <p>Abstract</p> <p>Background</p> <p>Mitochondrial DNA (mtDNA) mutations are of increasing interest due to their involvement in aging, disease, fertility, and their role in the evolution of the mitochondrial genome. The presence of reactive oxygen species and the near lack of repair mechanisms cause mtDNA to mutate at a faster rate than nuclear DNA, and mtDNA deletions are not uncommon in the tissues of individuals, although germ-line mtDNA is largely lesion-free. Large-scale deletions in mtDNA may disrupt multiple genes, and curiously, some large-scale deletions persist over many generations in a heteroplasmic state. Here we examine the phenotypic effects of one such deletion, <it>uaDf5</it>, in <it>Caenorhabditis elegans </it>(<it>C. elegans</it>). Our study investigates the phenotypic effects of this 3 kbp deletion.</p> <p>Results</p> <p>The proportion of <it>uaDf5 </it>chromosomes in worms was highly heritable, although <it>uaDf5 </it>content varied from worm to worm and within tissues of individual worms. We also found an impact of the <it>uaDf5 </it>deletion on metabolism. The deletion significantly reduced egg laying rate, defecation rate, and lifespan. Examination of sperm bearing the <it>uaDf5 </it>deletion revealed that sperm crawled more slowly, both in <it>vitro </it>and <it>in vivo</it>.</p> <p>Conclusion</p> <p>Worms harboring <it>uaDf5 </it>are at a selective disadvantage compared to worms with wild-type mtDNA. These effects should lead to the rapid extinction of the deleted chromosome, but it persists indefinitely. We discuss both the implications of this phenomenon and the possible causes of a shortened lifespan for <it>uaDf5 </it>mutant worms.</p>
url http://www.biomedcentral.com/1471-2156/8/8
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