The Barcode Blog

A mostly scientific blog about short DNA sequences for species identification and discovery. I encourage your commentary. -- Mark Stoeckle

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Mitochondrial DNA’s unique power

The DNA barcode for animals is a 648 base pair (bp) fragment from the 5′ end of mitochondrial gene cytochrome c oxidase subunit I (COI).  Does this relatively short mitochondrial sequence contain enough information to make evolutionary inferences about species limits, or is it a more of a rough survey method that needs to be confirmed by more data including from nuclear genes? 

In April 2008 Mol Ecol researchers from University of Minnesota and American Museum of Natural History, New York, analyze utility of mitochondrial as compared to nuclear DNA for inferring recent evolutionary history. Zink and Barrowclough first apply population genetic theory and then look at real data from bird species. 

Based on mathematical population genetics, they find “mitochondrial loci are generally a more sensitive indicator of population structure than are nuclear loci,” primarily due to much smaller effective population size (Ne) for mitochondrial as compared to nuclear markers, which leads to more rapid sorting of differences among genetically isolated populations. Analysis of real-world data in 45 studies of differences among and within avian species confirms this expectation, ie either the patterning is consistent between mitochondrial and nuclear genes, or there are shallow mtDNA trees which are not yet reflected in nuclear genes. Reanalysis of one study, which appears to show a split in nuclear but not mitochondrial markers, suggests possible misinterpretation. Regarding other factors that could potentially lead to mistaken inferences about species limits based on mitochondrial DNA (NUMTs, sex-biased gene flow, introgression), experimental data suggests these are rarely important, at least in birds. The authors conclude “mtDNA patterns will prove to be robust indicators of population history and species limits.” Nuclear markers ARE important for deep gene trees, for detecting hybrids, and for “quantitative estimates…of rates of population growth and values of gene flow.”  

Regarding length of mitochondrial sequence, this only has to be long enough to capture differences among closely-related species. Most populations that we recognize as species differ from their closest relatives by >1% in mitochondrial coding regions (corresponding to about 0.5 million years or more of reproductive isolation). At this level, even 100 bp is generally sufficient to distinguish most closely-related species, and a 648 bp COI barcode sequence should generally allow resolution of populations/species which have been reproductively isolated for much shorter periods of time. 

This entry was posted on Sunday, July 20th, 2008 at 5:03 pm and is filed under General. You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed.

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Contact: mark.stoeckle@rockefeller.edu

About this site

This web site is an outgrowth of the Taxonomy, DNA, and Barcode of Life meeting held at Banbury Center, Cold Spring Harbor Laboratory, September 9-12, 2003. It is designed and managed by Mark Stoeckle, Perrin Meyer, and Jason Yung at the Program for the Human Environment (PHE) at The Rockefeller University.

About the Program for the Human Environment

The involvement of the Program for the Human Environment in DNA barcoding dates to Jesse Ausubel's attendance in February 2002 at a conference in Nova Scotia organized by the Canadian Center for Marine Biodiversity. At the conference, Paul Hebert presented for the first time his concept of large-scale DNA barcoding for species identification. Impressed by the potential for this technology to address difficult challenges in the Census of Marine Life, Jesse agreed with Paul on encouraging a conference to explore the contribution taxonomy and DNA could make to the Census as well as other large-scale terrestrial efforts. In his capacity as a Program Director of the Sloan Foundation, Jesse turned to the Banbury Conference Center of Cold Spring Harbor Laboratory, whose leader Jan Witkowski prepared a strong proposal to explore both the scientific reliability of barcoding and the processes that might bring it to broad application. Concurrently, PHE researcher Mark Stoeckle began to work with the Hebert lab on analytic studies of barcoding in birds. Our involvement in barcoding now takes 3 forms: assisting the organizational development of the Consortium for the Barcode of Life and the Barcode of Life Initiative; contributing to the scientific development of the field, especially by studies in birds, and contributing to public understanding of the science and technology of barcoding and its applications through improved visualization techniques and preparation of brochures and other broadly accessible means, including this website. While the Sloan Foundation continues to support CBOL through a grant to the Smithsonian Institution, it does not provide financial support for barcoding research itself or support to the PHE for its research in this field.