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      Blurring the Boundaries between a Branch and a Flower: Potential Developmental Venues in CACTACEAE

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          Abstract

          Flowers are defined as short shoots that carry reproductive organs. In Cactaceae, this term acquires another meaning, since the flower is interpreted as a branch with a perianth at the tip, with all reproductive organs embedded within the branch, thus giving way to a structure that has been called a “flower shoot”. These organs have long attracted the attention of botanists and cactologists; however, the understanding of the morphogenetic processes during the development of these structures is far from clear. In this review, we present and discuss some classic flower concepts used to define floral structures in Cactaceae in the context of current advances in flower developmental genetics and evolution. Finally, we propose several hypotheses to explain the origin of these floral shoot structures in cacti, and we suggest future research approaches and methods that could be used to fill the gaps in our knowledge regarding the ontogenetic origin of the “flower” in the cactus family.

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          Most cited references114

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          Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.

          Mutations in CUC1 and CUC2 (for CUP-SHAPED COTYLEDON), which are newly identified genes of Arabidopsis, caused defects in the separation of cotyledons (embryonic organs), sepals, and stamens (floral organs) as well as in the formation of shoot apical meristems. These defects were most apparent in the double mutant. Phenotypes of the mutants suggest a common mechanism for separating adjacent organs within the same whorl in both embryos and flowers. We cloned the CUC2 gene and found that the encoded protein was homologous to the petunia NO APICAL MERISTEM (NAM) protein, which is thought to act in the development of embryos and flowers.
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            The no apical meristem gene of Petunia is required for pattern formation in embryos and flowers and is expressed at meristem and primordia boundaries.

            Petunia embryos carrying the no apical meristem (nam) mutation fail to develop a shoot apical meristem. Occasional shoots on nam- seedlings bear flowers that develop ten instead of five primordia in the second whorl. Double mutants with the homeotic gene green petals show that nam acts independently of organ identify in whorl 2 and now also affects primordium number in whorl 3. The nam gene was isolated by transposon tagging. The encoded protein shares a conserved N-terminal domain with several other proteins of unknown function and thus represents a novel class of proteins. Strikingly, nam mRNA accumulates in cells at the boundaries of meristems and primordia. These data indicate a role for nam in determining positions of meristems and primordia.
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              Origin of angiosperms and the puzzle of the Jurassic gap

              Angiosperms are by far the most species-rich clade of land plants, but their origin and early evolutionary history remain poorly understood. We reconstructed angiosperm phylogeny based on 80 genes from 2,881 plastid genomes representing 85% of extant families and all orders. With a well-resolved plastid tree and 62 fossil calibrations, we dated the origin of the crown angiosperms to the Upper Triassic, with major angiosperm radiations occurring in the Jurassic and Lower Cretaceous. This estimated crown age is substantially earlier than that of unequivocal angiosperm fossils, and the difference is here termed the 'Jurassic angiosperm gap'. Our time-calibrated plastid phylogenomic tree provides a highly relevant framework for future comparative studies of flowering plant evolution.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Plants (Basel)
                Plants (Basel)
                plants
                Plants
                MDPI
                2223-7747
                03 June 2021
                June 2021
                : 10
                : 6
                : 1134
                Affiliations
                [1 ]Instituto de Biología, Jardín Botánico, Universidad Nacional Autónoma de México, Ciudad de México C.P.04510, Mexico; isaurarosas@ 123456ciencias.unam.mx (I.R.-R.); urosas@ 123456ib.unam.mx (U.R.)
                [2 ]Posgrado en Ciencias Biológicas, Instituto de Biología, Universidad Nacional Autónoma de México, A. P. 70-153, Ciudad de México C.P.04510, Mexico
                [3 ]Departamento de Producción Agrícola y Animal, Universidad Autónoma Metropolitana-Xochimilco, Ciudad de México C.P.04510, Mexico; almapineyro@ 123456gmail.com
                [4 ]Centro de Ciencias de la Complejidad (C3), Universidad Nacional Autónoma de México, Ciudad de México C.P.04960, Mexico
                Author notes
                [* ]Correspondence: sarias@ 123456ib.unam.mx
                Author information
                https://orcid.org/0000-0001-5397-0666
                https://orcid.org/0000-0001-7349-0096
                https://orcid.org/0000-0001-5088-2679
                https://orcid.org/0000-0002-7674-7050
                Article
                plants-10-01134
                10.3390/plants10061134
                8228900
                34204904
                506105d4-f700-42b9-b0b1-2e1f0d309c47
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 14 May 2021
                : 01 June 2021
                Categories
                Review

                flower development,floral shoot,flower evolution,cacti evolution,evo-devo,flower organ identity

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