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      Delphinium as a model for development and evolution of complex zygomorphic flowers

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          Abstract

          The complex zygomorphic flowers of the early-diverging eudicot Delphinium provide an opportunity to explore intriguing evolutionary, developmental, and genetic questions. The dorsal perianth organs, consisting of a spurred sepal and the nectar-bearing spurred petal(s) in Delphinium, contribute to the dorso-ventralization and zygomorphic flower morphology. The seamless integration of the two or three dorsal petaloid spurred organs is considered a synorganization, and the resulting organ complex is referred to as a hyperorgan. The hyperorgan shows variability within the tribe due to variation in the number, size, and shape of the spurs. Research in recent decades within this tribe has enhanced our understanding of morphological evolution of flowers. More recently, functional studies using the RNAi approach of Virus-Induced Gene Silencing (VIGS) have unraveled interesting results highlighting the role of gene duplication in the functional diversification of organ identity and symmetry genes. Research in this early-diverging eudicot genus bridges the gaps in understanding the morphological innovations that are mostly studied in model grass and core eudicot clades. This first comprehensive review synthesizes eco-evo-devo research on Delphinium, developing a holistic understanding of recent advancements and establishing the genus as an exceptional model for addressing fundamental questions in developmental genetics, particularly in the evolution of complex flowers. This progress highlights Delphinium’s significant potential for future studies in this field.

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          The number of known plants species in the world and its annual increase

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            Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms.

            Although great progress has been made in clarifying deep-level angiosperm relationships, several early nodes in the angiosperm branch of the Tree of Life have proved difficult to resolve. Perhaps the last great question remaining in basal angiosperm phylogeny involves the branching order among the five major clades of mesangiosperms (Ceratophyllum, Chloranthaceae, eudicots, magnoliids, and monocots). Previous analyses have found no consistent support for relationships among these clades. In an effort to resolve these relationships, we performed phylogenetic analyses of 61 plastid genes ( approximately 42,000 bp) for 45 taxa, including members of all major basal angiosperm lineages. We also report the complete plastid genome sequence of Ceratophyllum demersum. Parsimony analyses of combined and partitioned data sets varied in the placement of several taxa, particularly Ceratophyllum, whereas maximum-likelihood (ML) trees were more topologically stable. Total evidence ML analyses recovered a clade of Chloranthaceae + magnoliids as sister to a well supported clade of monocots + (Ceratophyllum + eudicots). ML bootstrap and Bayesian support values for these relationships were generally high, although approximately unbiased topology tests could not reject several alternative topologies. The extremely short branches separating these five lineages imply a rapid diversification estimated to have occurred between 143.8 +/- 4.8 and 140.3 +/- 4.8 Mya.
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              Complexes of MADS-box proteins are sufficient to convert leaves into floral organs.

              T Honma, K Goto (2001)
              Genetic studies, using floral homeotic mutants, have led to the ABC model of flower development. This model proposes that the combinatorial action of three sets of genes, the A, B and C function genes, specify the four floral organs (sepals, petals, stamens and carpels) in the concentric floral whorls. However, attempts to convert vegetative organs into floral organs by altering the expression of ABC genes have been unsuccessful. Here we show that the class B proteins of Arabidopsis, PISTILLATA (PI) and APETALA3 (AP3), interact with APETALA1 (AP1, a class A protein) and SEPALLATA3 (SEP3, previously AGL9), and with AGAMOUS (AG, a class C protein) through SEP3. We also show that vegetative leaves of triply transgenic plants, 35S::PI;35S::AP3;35S::AP1 or 35S::PI;35S::AP3;35S::SEP3, are transformed into petaloid organs and that those of 35S::PI;35S::AP3;35S::SEP3;35S::AG are transformed into staminoid organs. Our findings indicate that the formation of ternary and quaternary complexes of ABC proteins may be the molecular basis of the ABC model, and that the flower-specific expression of SEP3 restricts the action of the ABC genes to the flower.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/493984Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:
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                URI : https://loop.frontiersin.org/people/2775567Role: Role: Role: Role:
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                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                19 August 2024
                2024
                : 15
                : 1453951
                Affiliations
                [1] Department of Biological Sciences, California State Polytechnic University , Pomona, CA, United States
                Author notes

                Edited by: Verónica S. Di Stilio, University of Washington, United States

                Reviewed by: Florian Jabbour, Muséum National d’Histoire Naturelle, France

                Aniket Sengupta, St. John’s University, United States

                *Correspondence: Bharti Sharma, bsharma@ 123456cpp.edu
                Article
                10.3389/fpls.2024.1453951
                11366623
                39224845
                1a0931c1-d48f-45d5-be83-67e5395f9929
                Copyright © 2024 Sharma, Pandher, Alcaraz Echeveste, Romo and Bravo

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 24 June 2024
                : 29 July 2024
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 78, Pages: 12, Words: 6413
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. BS is supported by the Provost Teacher-Scholar Award, Strategic Interdisciplinary Research Grant, and Agriculture Research Institute grant 20-04-122. This project was supported by an USDA NIFA Hispanic Serving Institution grant to the California State University Agricultural Research Institute, award number 2019-38422-30208 to MP and RR. MP and RR are also supported by the CPP STARS Program. AEQA- Is supported through Grant no- T32GM137812 through NIH, B2D program. MB is supported by McNair Scholars Program.
                Categories
                Plant Science
                Review
                Custom metadata
                Plant Development and EvoDevo

                Plant science & Botany
                delphinium,zygomorphy,synorganization,model system,evo-devo,petaloid spurs
                Plant science & Botany
                delphinium, zygomorphy, synorganization, model system, evo-devo, petaloid spurs

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