109
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Exploring the evolutionary origin of floral organs of Erycina pusilla, an emerging orchid model system

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Thousands of flowering plant species attract pollinators without offering rewards, but the evolution of this deceit is poorly understood. Rewardless flowers of the orchid Erycina pusilla have an enlarged median sepal and incised median petal (‘lip’) to attract oil-collecting bees. These bees also forage on similar looking but rewarding Malpighiaceae flowers that have five unequally sized petals and gland-carrying sepals. The lip of E. pusilla has a ‘callus’ that, together with winged ‘stelidia’, mimics these glands. Different hypotheses exist about the evolutionary origin of the median sepal, callus and stelidia of orchid flowers.

          Results

          The evolutionary origin of these organs was investigated using a combination of morphological, molecular and phylogenetic techniques to a developmental series of floral buds of E. pusilla. The vascular bundle of the median sepal indicates it is a first whorl organ but its convex epidermal cells reflect convergence of petaloid features. Expression of AGL6 EpMADS4 and APETALA3 EpMADS14 is low in the median sepal, possibly correlating with its petaloid appearance. A vascular bundle indicating second whorl derivation leads to the lip. AGL6 EpMADS5 and APETALA3 EpMADS13 are most highly expressed in lip and callus, consistent with current models for lip identity. Six vascular bundles, indicating a stamen-derived origin, lead to the callus, stelidia and stamen. AGAMOUS is not expressed in the callus, consistent with its sterilization. Out of three copies of AGAMOUS and four copies of SEPALLATA, EpMADS22 and EpMADS6 are most highly expressed in the stamen. Another copy of AGAMOUS, EpMADS20, and the single copy of SEEDSTICK, EpMADS23, are most highly expressed in the stelidia, suggesting EpMADS22 may be required for fertile stamens.

          Conclusions

          The median sepal, callus and stelidia of E. pusilla appear to be derived from a sepal, a stamen that gained petal identity, and stamens, respectively. Duplications, diversifying selection and changes in spatial expression of different MADS-box genes shaped these organs, enabling the rewardless flowers of E. pusilla to mimic an unrelated rewarding flower for pollinator attraction. These genetic changes are not incorporated in current models and urge for a rethinking of the evolution of deceptive flowers.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12862-017-0938-7) contains supplementary material, which is available to authorized users.

          Related collections

          Most cited references55

          • Record: found
          • Abstract: found
          • Article: not found

          Control of leaf vascular patterning by polar auxin transport.

          The formation of the leaf vascular pattern has fascinated biologists for centuries. In the early leaf primordium, complex networks of procambial cells emerge from homogeneous subepidermal tissue. The molecular nature of the underlying positional information is unknown, but various lines of evidence implicate gradually restricted transport routes of the plant hormone auxin in defining sites of procambium formation. Here we show that a crucial member of the AtPIN family of auxin-efflux-associated proteins, AtPIN1, is expressed prior to pre-procambial and procambial cell fate markers in domains that become restricted toward sites of procambium formation. Subcellular AtPIN1 polarity indicates that auxin is directed to distinct "convergence points" in the epidermis, from where it defines the positions of major veins. Integrated polarities in all emerging veins indicate auxin drainage toward pre-existing veins, but veins display divergent polarities as they become connected at both ends. Auxin application and transport inhibition reveal that convergence point positioning and AtPIN1 expression domain dynamics are self-organizing, auxin-transport-dependent processes. We derive a model for self-regulated, reiterative patterning of all vein orders and postulate at its onset a common epidermal auxin-focusing mechanism for major-vein positioning and phyllotactic patterning.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Development of floral organ identity: stories from the MADS house.

            Recent studies on AGAMOUS-LIKE2-, DEFICIENS- and GLOBOSA-like MADS-box genes in diverse seed plant species have provided novel insights into the mechanisms by which the identity of the different floral organs is specified during flower development. These advances in understanding may lead to major refinements in the classical ABC model of floral organ identity.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The genome sequence of the orchid Phalaenopsis equestris.

              Orchidaceae, renowned for its spectacular flowers and other reproductive and ecological adaptations, is one of the most diverse plant families. Here we present the genome sequence of the tropical epiphytic orchid Phalaenopsis equestris, a frequently used parent species for orchid breeding. P. equestris is the first plant with crassulacean acid metabolism (CAM) for which the genome has been sequenced. Our assembled genome contains 29,431 predicted protein-coding genes. We find that contigs likely to be underassembled, owing to heterozygosity, are enriched for genes that might be involved in self-incompatibility pathways. We find evidence for an orchid-specific paleopolyploidy event that preceded the radiation of most orchid clades, and our results suggest that gene duplication might have contributed to the evolution of CAM photosynthesis in P. equestris. Finally, we find expanded and diversified families of MADS-box C/D-class, B-class AP3 and AGL6-class genes, which might contribute to the highly specialized morphology of orchid flowers.
                Bookmark

                Author and article information

                Contributors
                anita.dirks@naturalis.nl
                roland.butot@naturalis.nl
                schaik.van.peter@gmail.com
                janwillem.wijnands@gmail.com
                rca.vd.berg@outlook.com
                louie.krol.jr@gmail.com
                sadhanadoebar@gmail.com
                k.vankooperen@gmail.com
                h.d.boer@nhm.uio.no
                ekramer@oeb.harvard.edu
                erik.smets@naturalis.nl
                rutger.vos@naturalis.nl
                alexander.vrijdaghs@bio.kuleuven.be
                Barbara.Gravendeel@naturalis.nl
                Journal
                BMC Evol Biol
                BMC Evol. Biol
                BMC Evolutionary Biology
                BioMed Central (London )
                1471-2148
                23 March 2017
                23 March 2017
                2017
                : 17
                : 89
                Affiliations
                [1 ]ISNI 0000 0001 2159 802X, GRID grid.425948.6, , Endless Forms group, Naturalis Biodiversity Center, ; Vondellaan 55, 2332 AA Leiden, The Netherlands
                [2 ]GRID grid.449761.9, , Faculty of Science and Technology, University of Applied Sciences Leiden, ; Zernikedreef 11, 2333 CK Leiden, The Netherlands
                [3 ]ISNI 000000041936754X, GRID grid.38142.3c, Department of Organismic and Evolutionary Biology, , Harvard University, ; 16 Divinity Ave, Cambridge, MA 02138 USA
                [4 ]ISNI 0000000084992262, GRID grid.7177.6, Institute for Biodiversity and Ecosystem Dynamics, , University of Amsterdam, ; Science Park 904, 1098 XH Amsterdam, The Netherlands
                [5 ]ISNI 0000 0001 2312 1970, GRID grid.5132.5, Institute Biology Leiden, , Leiden University, ; Sylviusweg 72, 2333 BE Leiden, The Netherlands
                [6 ]ISNI 0000 0001 0668 7884, GRID grid.5596.f, Ecology, Evolution and Biodiversity Conservation cluster, , KU Leuven, ; Kasteelpark Arenberg 31, 3001 Leuven, Belgium
                [7 ]ISNI 0000 0004 1936 8921, GRID grid.5510.1, The Natural History Museum, , University of Oslo, ; P.O. Box 1172, Blindern, 0318 Oslo, Norway
                [8 ]ISNI 0000 0004 1936 9457, GRID grid.8993.b, Department of Organismal Biology, Evolutionary Biology Centre, , Uppsala University, ; Norbyvägen 18D, Uppsala, SE-75236 Sweden
                Author information
                http://orcid.org/0000-0002-6508-0895
                Article
                938
                10.1186/s12862-017-0938-7
                5364718
                28335712
                1f5888f2-37a2-45c0-b47f-f5eff32afd7b
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 29 September 2016
                : 15 March 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003246, Nederlandse Organisatie voor Wetenschappelijk Onderzoek;
                Award ID: 023.003.015
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                Evolutionary Biology
                deceptive pollination,floral development,mads-box genes,mimicry,vascular bundles

                Comments

                Comment on this article