Barcoding of Bromeliaceae (Poales) - IBOL 2017 · Bromeliaceae will be provided based on the...

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Barcoding of Bromeliaceae (Poales) 1,2 Cyrannek, N., 1,2 Heller, S., 3 Leme, E.M.C., 1,2 Favre, A., 1,2 Paule, J., 4 Koch, M. & 1,2 Zizka, G. 1 Department Botany and Molecular Evolution, Senckenberg Research Institute Frankfurt, Germany 2 Institute Ecology, Evolution and Diversity, Faculty Biosciences, Goethe University Frankfurt, Germany 3 Marie Selby Botanical Gardens, Sarasota, Florida, USA 4 Center of Organismal Studies, University Heidelberg, Germany Background The angiosperm family Bromeliaceae comprises 3912 species (Butcher & Gouda 2017: http://botu07.bio.uu.nl/bcg/taxonList.php), almost all of them restricted to the Neotropics (a single species is native to West Africa). The family is characterized by exceptionally high morphological and ecological diversity as well as a very low DNA sequence variability. Most of the species are monocarpic, propagating vegetatively with lateral shoots. In several genera, plants are vegetatively very similar, which makes determination of bromeliads difficult (fig. 2). Especially in Botanic Gardens this is a problem, when plants are cultivated several years before flowering. Barcoding is a very promising approach to provide fast and cheap determination of bromeliads, however, the observed low genetic variability causes specific problems. Results In the course of a project (Evo-BoGa) funded by the German Federal Ministry of Education and Research (BMBF) to improve access and scientific use of living collections, a number of DNA markers was tested for their suitability for barcoding (nuclear: agt1, ETS, phyC; plastid: matK, ycf1, trnL-F, psbA- trnH). The highly variable nuclear marker agt1 was identified as suitable barcode marker for identification. Significance The barcoding approach will improve the availability of bromeliad collections in Botanic Gardens. Outlook At present, app. 400 species of subfamily Bromelioideae have been barcoded, app. further 500 species will be sequenced in the course of the project. A special web-portal for Bromeliaceae will be provided based on the BrassiBase database (URL: https://brassibase.cos.uni-heidelberg.de). Acknowledgements Federal Minstery of Education and Research Epiphytic bromeliad diversity in Panama (Foto: Daniel Caceres). Guzmania musaica, a tank forming bromeliad in flower (Foto: Daniel Caceres). Bromeliad collection in the private Botanic Garden “Refúgio do Gravatás” in Teresopolis. Note morphological similarity and very few specimens in flower (Foto: Sascha Heller). Alignment of agt1 with a highly variable part (left), a large indel (center) and the highly conserved part (right). Pairwise sequence similarity for agt1 for selected species of Bromelioideae throughout the subfamily. The marker agt1 showed exceptional variability. Other recommended barcoding markers for plants (e.g. matK, rbcL, psbA-trnH) did not provide sufficient resolution. ID 435

Transcript of Barcoding of Bromeliaceae (Poales) - IBOL 2017 · Bromeliaceae will be provided based on the...

Page 1: Barcoding of Bromeliaceae (Poales) - IBOL 2017 · Bromeliaceae will be provided based on the BrassiBase database (URL: ). Acknowledgements Federal Minstery of Education and Research

Barcoding of Bromeliaceae (Poales) 1,2 Cyrannek, N., 1,2 Heller, S., 3Leme, E.M.C., 1,2 Favre, A., 1,2 Paule, J., 4 Koch, M. & 1,2 Zizka, G.

1 Department Botany and Molecular Evolution, Senckenberg Research Institute Frankfurt, Germany 2 Institute Ecology, Evolution and Diversity, Faculty Biosciences, Goethe University Frankfurt, Germany

3 Marie Selby Botanical Gardens, Sarasota, Florida, USA 4 Center of Organismal Studies, University Heidelberg, Germany

Background

The angiosperm family Bromeliaceae comprises 3912 species (Butcher

& Gouda 2017: http://botu07.bio.uu.nl/bcg/taxonList.php), almost all of

them restricted to the Neotropics (a single species is native to West

Africa). The family is characterized by exceptionally high morphological

and ecological diversity as well as a very low DNA sequence variability.

Most of the species are monocarpic, propagating vegetatively with

lateral shoots. In several genera, plants are vegetatively very similar,

which makes determination of bromeliads difficult (fig. 2). Especially in

Botanic Gardens this is a problem, when plants are cultivated several

years before flowering. Barcoding is a very promising approach to

provide fast and cheap determination of bromeliads, however, the

observed low genetic variability causes specific problems.

Results

In the course of a project (Evo-BoGa)

funded by the German Federal Ministry of

Education and Research (BMBF) to improve

access and scientific use of living collections,

a number of DNA markers was tested for

their suitability for barcoding (nuclear: agt1,

ETS, phyC; plastid: matK, ycf1, trnL-F, psbA-

trnH).

The highly variable nuclear marker agt1 was

identified as suitable barcode marker for

identification.

Significance

The barcoding approach will improve the

availability of bromeliad collections in Botanic

Gardens.

Outlook

At present, app. 400 species of subfamily

Bromelioideae have been barcoded, app.

further 500 species will be sequenced in the

course of the project. A special web-portal for

Bromeliaceae will be provided based on the

BrassiBase database

(URL: https://brassibase.cos.uni-heidelberg.de).

Acknowledgements

Federal Minstery of

Education and Research

Epiphytic bromeliad diversity in Panama (Foto: Daniel Caceres).

Guzmania musaica, a tank forming bromeliad in flower (Foto: Daniel

Caceres).

Bromeliad collection in the private Botanic Garden “Refúgio do Gravatás” in Teresopolis. Note morphological similarity and very few

specimens in flower (Foto: Sascha Heller).

Alignment of agt1 with a highly variable part (left), a large indel (center) and the highly conserved part (right).

Pairwise sequence similarity for agt1 for selected species of Bromelioideae throughout the subfamily. The marker agt1 showed

exceptional variability. Other recommended barcoding markers for plants (e.g. matK, rbcL, psbA-trnH) did not provide sufficient

resolution.

ID 435