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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Pieces of a puzzle

Why DNA barcoding works as well as it does is an unsolved scientific puzzle. It is long observed that mitochondrial DNA differences within animal species are generally much smaller than those among species and, in the landscape of phylogenetic trees, mitochondrial DNA sequences of most species form single clusters distinct from those of other species. As a result “mtDNA data and traditional taxonomic assignments tend to converge on what may be “real” biotic units in nature”  (Avise and Walker 1999 Proc Natl Acad Sci USA 96:992). Although Avise and Walker’s original observation was largely based on terrestrial, temperate zone vertebrates, growing barcode libraries demonstrate similar patterning in diverse invertebrates, vertebrates, and protists in marine and terrestrial environments, and in tropical and temperate zones, and in at least some fungi and plants (see last week’s post on COI barcodes in red algae

Smith et al 2004 Science 305:371What underlies the usual patterning of small differences within and large differences among most animal species? The unsolved puzzle is how to reconcile these two findings. Large differences among closely-related species indicates mitochondrial DNA undergoes rapid sequence evolution, and there are reasonable mechanistic explanations for why this might be so. On the other hand, rapid sequence evolution should also lead to accumulation of sequence diversity within species over time and in those with large populations. Instead the data shows a relative absence of variation within most species, including those thought to be ancient and those with enormous population sizes. I will set aside two of the usual suspects: population bottlenecks and small effective population size. Population bottlenecks are implausible given the diversity of species showing this pattern. Postulating a small effective population size is a restatement of the finding of absence of variation, not an explanation. 

This table-napkin analysis leads me to selective sweeps as pruning mitochondrial diversity within species (eg Bazin et al 2006 Science 312:570, see also editorial and reader commentary). If selective sweeps restrict mitochondrial diversity, then the question becomes what is being selected for? Environmental adaptation seems unlikely, as restricted variation is seen in species that are as best one can tell morphologically and ecologically unchanged (eg see earlier posts on horseshoe crabs, salamanders). It might be there is little tolerance for genetic variation due to interactions of mitochondrial proteins with other cellular components, but if so there should be species with genetic stasis in mitochondrial DNA, just as there are many species with apparent morphologic stasis. However, in simple distance trees most species show roughly similar genetic distances. 

I am intrigued by a time series of influenza A hemagglutinin gene evolution which reflects competition between virus and host and wonder if there might be some kind of competition that helps drive mitochondrial sequence evolution forward and at the same time suppresses variation. It is exciting there will be an EMBO workshop “Molecular Biodiversity and DNA Barcodes” May 2007 in Rome which may help answer scientific questions posed by DNA barcode data.

This entry was posted on Thursday, December 28th, 2006 at 11:56 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.