Relaxation of selective constraints on avian mitochondrial DNA following the degeneration of flight ability
- Yong-Yi Shen1,2,3,
- Peng Shi1,4,
- Yan-Bo Sun1,2,3 and
- Ya-Ping Zhang1,2,4
- 1 State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, The Chinese Academy of Sciences, Kunming 650223, China;
- 2 Laboratory for Conservation and Utilization of Bio-Resources, Yunnan University, Kunming 650091, China;
- 3 Graduate School of the Chinese Academy of Sciences, Beijing 100039, China
Abstract
The evolution of flight is the most important feature of birds, and this ability has helped them become one of the most successful groups of vertebrates. However, some species have independently lost their ability to fly. The degeneration of flight ability is a long process, and some species remain transitional locomotive models. Most of the energy required for locomotion is supplied by mitochondria via oxidative phosphorylation. Thus, rapidly flying birds should require a more energy efficient metabolism than weakly flying or flightless species. Therefore, we speculated that evolutionary constraints acted on the mtDNA of birds with different locomotive abilities. To test this hypothesis, we compared 76 complete avian mitochondrial genomes. Weakly flying and flightless birds, compared to rapidly flying birds, accumulated more nonsynonymous nucleotide substitutions relative to synonymous substitutions. Even after controlling for mutation rate, this trend remained significant. This finding was further tested for its generality by examining 214 complete mammalian mitochondrial genomes. The same as birds, a negative correlation was also found for the Ka/Ks ratio and locomotive speed. Our results demonstrated that, in addition to the previously described role for effective population size, functional constraints due to locomotion play an important role in the evolution of mtDNA.
Footnotes
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↵4 Corresponding authors.
E-mail zhangyp{at}mail.kiz.ac.cn; fax 86-871-5195430.
E-mail ship{at}mail.kiz.ac.cn; fax 86-871-5199318.
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[Supplemental material is available online at http://www.genome.org. The sequence data from this study have been submitted to GenBank (http://www.ncbi.nlm.nih.gov/Genbank/) under accession nos. EU165706, EU165707, and EU417810–EU417812.]
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Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.093138.109.
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- Received February 15, 2009.
- Accepted June 16, 2009.
- Copyright © 2009 by Cold Spring Harbor Laboratory Press











