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      Evolution and development of three highly specialized floral structures of bee-pollinated Phalaenopsis species

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          Abstract

          Background

          Variation in shape and size of many floral organs is related to pollinators. Evolution of such organs is driven by duplication and modification of MADS-box and MYB transcription factors. We applied a combination of micro-morphological (SEM and micro 3D-CT scanning) and molecular techniques (transcriptome and RT-PCR analysis) to understand the evolution and development of the callus, stelidia and mentum, three highly specialized floral structures of orchids involved in pollination. Early stage and mature tissues were collected from flowers of the bee-pollinated Phalaenopsis equestris and Phalaenopsis pulcherrima, two species that differ in floral morphology: P. equestris has a large callus but short stelidia and no mentum, whereas P. pulcherrima has a small callus, but long stelidia and a pronounced mentum.

          Results

          Our results show the stelidia develop from early primordial stages, whereas the callus and mentum develop later. In combination, the micro 3D-CT scan analysis and gene expression analyses show that the callus is of mixed petaloid-staminodial origin, the stelidia of staminodial origin, and the mentum of mixed sepaloid-petaloid-staminodial origin. SEP clade 1 copies are expressed in the larger callus of P. equestris, whereas AP3 clade 1 and AGL6 clade 1 copies are expressed in the pronounced mentum and long stelidia of P. pulcherrima. AP3 clade 4, PI-, AGL6 clade 2 and PCF clade 1 copies might have a balancing role in callus and gynostemium development. There appears to be a trade-off between DIV clade 2 expression with SEP clade 1 expression in the callus, on the one hand, and with AP3 clade 1 and AGL6 clade 1 expression in the stelidia and mentum on the other.

          Conclusions

          We detected differential growth and expression of MADS box AP3/PI-like, AGL6-like and SEP-like, and MYB DIV-like gene copies in the callus, stelidia and mentum of two species of Phalaenopsis, of which these floral structures are very differently shaped and sized. Our study provides a first glimpse of the evolutionary developmental mechanisms driving adaptation of Phalaenopsis flowers to different pollinators by providing combined micro-morphological and molecular evidence for a possible sepaloid–petaloid–staminodial origin of the orchid mentum.

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          Most cited references61

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          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.
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            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.
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              The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity.

              The ABC model of flower organ identity is widely recognized as providing a framework for understanding the specification of flower organs in diverse plant species. Recent studies in Arabidopsis thaliana have shown that three closely related MADS-box genes, SEPALLATA1 (SEP1), SEP2 and SEP3, are required to specify petals, stamens, and carpels because these organs are converted into sepals in sep1 sep2 sep3 triple mutants. Additional studies indicate that the SEP proteins form multimeric complexes with the products of the B and C organ identity genes. Here, we characterize the SEP4 gene, which shares extensive sequence similarity to and an overlapping expression pattern with the other SEP genes. Although sep4 single mutants display a phenotype similar to that of wild-type plants, we find that floral organs are converted into leaf-like organs in sep1 sep2 sep3 sep4 quadruple mutants, indicating the involvement of all four SEP genes in the development of sepals. We also find that SEP4 contributes to the development of petals, stamens, and carpels in addition to sepals and that it plays an important role in meristem identity. These and other data demonstrate that the SEP genes play central roles in flower meristem identity and organ identity.
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                Author and article information

                Contributors
                Barbara.Gravendeel@naturalis.nl
                Journal
                EvoDevo
                Evodevo
                EvoDevo
                BioMed Central (London )
                2041-9139
                10 August 2020
                10 August 2020
                2020
                : 11
                : 16
                Affiliations
                [1 ]GRID grid.425948.6, ISNI 0000 0001 2159 802X, Naturalis Biodiversity Center, Endless Forms Group, ; Darwinweg 2, 2333 CR Leiden, The Netherlands
                [2 ]GRID grid.5132.5, ISNI 0000 0001 2312 1970, Intitute of Biology Leiden, Leiden University, ; Sylviusweg 72, 2333 BE Leiden, The Netherlands
                [3 ]Indonesian Ornamental Crops Research Institute (IOCRI), Jl. Raya Ciherang, Pacet-Cianjur, 43253 West Java Indonesia
                [4 ]GRID grid.449761.9, ISNI 0000 0004 0418 4775, Faculty of Science and Technology, , University of Applied Sciences Leiden, ; Zernikedreef 11, 2333 CK Leiden, The Netherlands
                [5 ]GRID grid.450078.e, ISNI 0000 0000 8809 2093, Life Sciences, HAN University of Applied Sciences, ; Ruitenbergerlaan 31, 6826 CC Arnhem, The Netherlands
                [6 ]GRID grid.5596.f, ISNI 0000 0001 0668 7884, Ecology, Evolution and Biodiversity Conservation, KU Leuven, ; Kasteelpark Arenberg 31, P.O. Box 2435, 3001 Heverlee, Belgium
                [7 ]GRID grid.5590.9, ISNI 0000000122931605, IWWR, Radboud University, ; Heyendaalseweg 135, 6500 GL Nijmegen, The Netherlands
                Author information
                http://orcid.org/0000-0002-6781-774X
                http://orcid.org/0000-0002-9416-983X
                http://orcid.org/0000-0002-6508-0895
                Article
                160
                10.1186/s13227-020-00160-z
                7418404
                32793330
                fe346e79-e700-4364-bd7b-b1c1e5c5c19a
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

                History
                : 14 March 2020
                : 29 June 2020
                Funding
                Funded by: SMARTD-IAARD, Kementerian Pertanian Republik Indonesia (ID)
                Categories
                Research
                Custom metadata
                © The Author(s) 2020

                Developmental biology
                callus,mentum,stelidia,rt-pcr,transcriptomics
                Developmental biology
                callus, mentum, stelidia, rt-pcr, transcriptomics

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