Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution

<p>Abstract</p> <p>Background</p> <p>The theory of Muller' Ratchet predicts that small asexual populations are doomed to accumulate ever-increasing deleterious mutation loads as a consequence of the magnified power of genetic drift and mutation that accompanies sma...

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Main Authors: Denver Dee R, Howe Dana K
Format: Article
Language:English
Published: BMC 2008-02-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/8/62
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spelling doaj-7a110a2c7c6642c0ae69d8a32424e89f2021-09-02T12:55:47ZengBMCBMC Evolutionary Biology1471-21482008-02-01816210.1186/1471-2148-8-62Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolutionDenver Dee RHowe Dana K<p>Abstract</p> <p>Background</p> <p>The theory of Muller' Ratchet predicts that small asexual populations are doomed to accumulate ever-increasing deleterious mutation loads as a consequence of the magnified power of genetic drift and mutation that accompanies small population size. Evidence for Muller's Ratchet and knowledge on its underlying molecular mechanisms, however, are lacking for natural populations.</p> <p>Results</p> <p>We characterized mitochondrial genome evolutionary processes in <it>Caenorhabditis briggsae </it>natural isolates to show that numerous lineages experience a high incidence of nonsynonymous substitutions in protein-coding genes and accumulate unusual deleterious noncoding DNA stretches with associated heteroplasmic function-disrupting genome deletions. Isolate-specific deletion proportions correlated negatively with nematode fecundity, suggesting that these deletions might negatively affect <it>C. briggsae </it>fitness. However, putative compensatory mutations were also observed that are predicted to reduce heteroplasmy levels of deleterious deletions. Paradoxically, compensatory mutations were observed in one major intraspecific <it>C. briggsae </it>clade where population sizes are estimated to be very small (and selection is predicted to be relatively weak), but not in a second major clade where population size estimates are much larger and selection is expected to be more efficient.</p> <p>Conclusion</p> <p>This study provides evidence that the mitochondrial genomes of animals evolving in nature are susceptible to Muller's Ratchet, suggests that context-dependent compensatory mutations can accumulate in small populations, and predicts that Muller's Ratchet can affect fundamental evolutionary forces such as the rate of mutation.</p> http://www.biomedcentral.com/1471-2148/8/62
collection DOAJ
language English
format Article
sources DOAJ
author Denver Dee R
Howe Dana K
spellingShingle Denver Dee R
Howe Dana K
Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution
BMC Evolutionary Biology
author_facet Denver Dee R
Howe Dana K
author_sort Denver Dee R
title Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution
title_short Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution
title_full Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution
title_fullStr Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution
title_full_unstemmed Muller's Ratchet and compensatory mutation in <it>Caenorhabditis briggsae </it>mitochondrial genome evolution
title_sort muller's ratchet and compensatory mutation in <it>caenorhabditis briggsae </it>mitochondrial genome evolution
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2008-02-01
description <p>Abstract</p> <p>Background</p> <p>The theory of Muller' Ratchet predicts that small asexual populations are doomed to accumulate ever-increasing deleterious mutation loads as a consequence of the magnified power of genetic drift and mutation that accompanies small population size. Evidence for Muller's Ratchet and knowledge on its underlying molecular mechanisms, however, are lacking for natural populations.</p> <p>Results</p> <p>We characterized mitochondrial genome evolutionary processes in <it>Caenorhabditis briggsae </it>natural isolates to show that numerous lineages experience a high incidence of nonsynonymous substitutions in protein-coding genes and accumulate unusual deleterious noncoding DNA stretches with associated heteroplasmic function-disrupting genome deletions. Isolate-specific deletion proportions correlated negatively with nematode fecundity, suggesting that these deletions might negatively affect <it>C. briggsae </it>fitness. However, putative compensatory mutations were also observed that are predicted to reduce heteroplasmy levels of deleterious deletions. Paradoxically, compensatory mutations were observed in one major intraspecific <it>C. briggsae </it>clade where population sizes are estimated to be very small (and selection is predicted to be relatively weak), but not in a second major clade where population size estimates are much larger and selection is expected to be more efficient.</p> <p>Conclusion</p> <p>This study provides evidence that the mitochondrial genomes of animals evolving in nature are susceptible to Muller's Ratchet, suggests that context-dependent compensatory mutations can accumulate in small populations, and predicts that Muller's Ratchet can affect fundamental evolutionary forces such as the rate of mutation.</p>
url http://www.biomedcentral.com/1471-2148/8/62
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