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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Reading DNA labels on sponges

Sponges are difficult to identify and classify. Many sponges “have a depauperate suite of morphologic characters and/or are plagued by morphological homoplasies” and vary according to environmental conditions, challenging identification at species level and stymying attempts to reconstruct evolutionary lineages.  In Dec 2007 J Marine Biol Assoc UK researchers from Geoscience Centre Gottingen, Germany, and Queensland Museum, Australia, report on how DNA can help. Worheide and Erpenbeck describe the nascent Sponge Barcoding Project www.spongebarcoding.org, which aims to collect DNA signature sequences [COI barcodes] from all 8,000 known marine intertidal, deep sea, and freshwater sponge taxa.  According to the authors “DNA barcoding will open up a new dimension and quality in biodiversity research and will become of vital importance for the survival and acknowledgement of sponge taxonomy and increase its reputation over the coming decades.” In addition to assisting species-level identifications, the authors posit the necessity of “DNA-assisted” taxonomy of sponges given the inability to construct convincing higher order classifications with morphologic characters.

An accompanying article analyzes COI barcode results for 166 specimens belonging to 65 species of Caribbean sponges. Similar to findings in other animal groups, the 584 bp COI fragment produced a gene tree similar to that with 28s rRNA, a slowly-evolving nuclear gene. In a ML analysis, some species had overlapping or shared sequences, which the authors point out may mean these are not “good species”, specimen identifications are incorrect, or that these species cannot be distinguished by a COI barcode alone. The sequences are published in GenBank and available individually through the Sponge Barcode website, and I hope the authors will also make their sequence and specimen data available on the Published Projects section of BOLD. This will allow access to the analytic and display software on the BOLD site, enable easy comparison of the sponge data set with that of other animals, and facilitate testing of other methods particularly for those species which are not distinguished in ML analysis.  

This entry was posted on Wednesday, December 12th, 2007 at 11:26 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.

3 Responses to “Reading DNA labels on sponges”

  1. Allen Says:

    It seems that it would be a nice addition to BOLD’s analysis capabilities if researchers could choose to have GenBank and EMBL sequences also included. This could be tagged or marked differently. While it is true that the standards for getting data into BOLD are more strict, data in these other databases are not necessarily substandard. The study to which you refer above also included other markers and it is much easier for researchers to put these data into GenBank or EMBL at once rather than have to go through the process of also submitting part of them to BOLD. (In this case, the COI data are in the Sponge Barcoding Project database which will feed into BOLD I believe, so it really is not much of an issue here.) One of BOLD’s major limitations is the restriction to this single COI marker. As everybody knows, for some groups this marker does not work as well as others for barcoding purposes. Some of us are very much anticipating the day when BOLD readily handles these other types of data.

  2. Joe Says:

    I never new that 28s rRNA was a slowly evolving gene! you learn something new every day…

  3. Mr. ADSL Says:

    Hmm I am also surprised about slow evolving gene, not that they exist (I study and searching on it now) but that 28s rRNA was one. I only knew it initiated polypeptide synthesis.

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.