Signaling Molecules in Plants: Exogenous Application
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Plant Physiology
PLANT PHYSIOLOGY Vince Ördög Created by XMLmind XSL-FO Converter. PLANT PHYSIOLOGY Vince Ördög Publication date 2011 Created by XMLmind XSL-FO Converter. Table of Contents Cover .................................................................................................................................................. v 1. Preface ............................................................................................................................................ 1 2. Water and nutrients in plant ............................................................................................................ 2 1. Water balance of plant .......................................................................................................... 2 1.1. Water potential ......................................................................................................... 3 1.2. Absorption by roots .................................................................................................. 6 1.3. Transport through the xylem .................................................................................... 8 1.4. Transpiration ............................................................................................................. 9 1.5. Plant water status .................................................................................................... 11 1.6. Influence of extreme water supply .......................................................................... 12 2. Nutrient supply of plant ..................................................................................................... -
Auxins and Cytokinins in Plant Development 2018
International Journal of Molecular Sciences Meeting Report Auxins and Cytokinins in Plant Development 2018 Jan Petrasek 1, Klara Hoyerova 1, Vaclav Motyka 1 , Jan Hejatko 2 , Petre Dobrev 1, Miroslav Kaminek 1 and Radomira Vankova 1,* 1 Laboratory of Hormonal Regulations in Plants, Institute of Experimental Botany, The Czech Academy of Sciences, Rozvojova 263, 16502 Prague 6, Czech Republic; [email protected] (J.P.); [email protected] (K.H.); [email protected] (V.M.); [email protected] (P.D.); [email protected] (M.K.) 2 CEITEC–Central European Institute of Technology and Functional Genomics and Proteomics, NCBR, Faculty of Science, Masaryk University, 62500 Brno, Czech Republic; [email protected] * Correspondence: [email protected]; Tel.: +420-225-106-427 Received: 15 February 2019; Accepted: 18 February 2019; Published: 20 February 2019 Abstract: The international symposium “Auxins and Cytokinins in Plant Development” (ACPD), which is held every 4–5 years in Prague, Czech Republic, is a meeting of scientists interested in the elucidation of the action of two important plant hormones—auxins and cytokinins. It is organized by a group of researchers from the Laboratory of Hormonal Regulations in Plants at the Institute of Experimental Botany, the Czech Academy of Sciences. The symposia already have a long tradition, having started in 1972. Thanks to the central role of auxins and cytokinins in plant development, the ACPD 2018 symposium was again attended by numerous experts who presented their results in the opening, two plenary lectures, and six regular sessions, including two poster sessions. Due to the open character of the research community, which is traditionally very well displayed during the meeting, a lot of unpublished data were presented and discussed. -
Endogenous Levels of Cytokinins, Indole-3-Acetic Acid And
www.nature.com/scientificreports OPEN Endogenous levels of cytokinins, indole-3-acetic acid and abscisic acid in in vitro grown potato: A contribution to potato hormonomics Martin Raspor 1,6*, Václav Motyka 2,6, Slavica Ninković 1, Petre I. Dobrev 2, Jiří Malbeck 3, Tatjana Ćosić 1, Aleksandar Cingel 1, Jelena Savić 1, Vojin Tadić 4 & Ivana Č. Dragićević 5 A number of scientifc reports published to date contain data on endogenous levels of various phytohormones in potato (Solanum tuberosum L.) but a complete cytokinin profle of potato tissues, that would include data on all particular molecular forms of cytokinin, has still been missing. In this work, endogenous levels of all analytically detectable isoprenoid cytokinins, as well as the auxin indole- 3-acetic acid (IAA), and abscisic acid (ABA) have been determined in shoots and roots of 30 day old in vitro grown potato (cv. Désirée). The results presented here are generally similar to other data reported for in vitro grown potato plants, whereas greenhouse-grown plants typically contain lower levels of ABA, possibly indicating that in vitro grown potato is exposed to chronic stress. Cytokinin N-glucosides, particularly N7-glucosides, are the dominant cytokinin forms in both shoots and roots of potato, whereas nucleobases, as the bioactive forms of cytokinins, comprise a low proportion of cytokinin levels in tissues of potato. Diferences in phytohormone composition between shoots and roots of potato suggest specifc patterns of transport and/or diferences in tissue-specifc metabolism of plant hormones. These results represent a contribution to understanding the hormonomics of potato, a crop species of extraordinary economic importance. -
Auxins Cytokinins and Gibberellins TD-I Date: 3/4/2019 Cell Enlargement in Young Leaves, Tissue Differentiation, Flowering, Fruiting, and Delay of Aging in Leaves
Informational TD-I Revision 2.0 Creation Date: 7/3/2014 Revision Date: 3/4/2019 Auxins, Cytokinins and Gibberellins Isolation of the first Cytokinin Growing cells in a tissue culture medium composed in part of coconut milk led to the realization that some substance in coconut milk promotes cell division. The “milk’ of the coconut is actually a liquid endosperm containing large numbers of nuclei. It was from kernels of corn, however, that the substance was first isolated in 1964, twenty years after its presence in coconut milk was known. The substance obtained from corn is called zeatin, and it is one of many cytokinins. What is a Growth Regulator? Plant Cell Growth regulators (e.g. Auxins, Cytokinins and Gibberellins) - Plant hormones play an important role in growth and differentiation of cultured cells and tissues. There are many classes of plant growth regulators used in culture media involves namely: Auxins, Cytokinins, Gibberellins, Abscisic acid, Ethylene, 6 BAP (6 Benzyladenine), IAA (Indole Acetic Acid), IBA (Indole-3-Butyric Acid), Zeatin and trans Zeatin Riboside. The Auxins facilitate cell division and root differentiation. Auxins induce cell division, cell elongation, and formation of callus in cultures. For example, 2,4-dichlorophenoxy acetic acid is one of the most commonly added auxins in plant cell cultures. The Cytokinins induce cell division and differentiation. Cytokinins promote RNA synthesis and stimulate protein and enzyme activities in tissues. Kinetin and benzyl-aminopurine are the most frequently used cytokinins in plant cell cultures. The Gibberellins is mainly used to induce plantlet formation from adventive embryos formed in culture. -
Development and Cell Cycle Activity of the Root Apical Meristem in the Fern Ceratopteris Richardii
G C A T T A C G G C A T genes Article Development and Cell Cycle Activity of the Root Apical Meristem in the Fern Ceratopteris richardii Alejandro Aragón-Raygoza 1,2 , Alejandra Vasco 3, Ikram Blilou 4, Luis Herrera-Estrella 2,5 and Alfredo Cruz-Ramírez 1,* 1 Molecular and Developmental Complexity Group at Unidad de Genómica Avanzada, Laboratorio Nacional de Genómica para la Biodiversidad, Cinvestav Sede Irapuato, Km. 9.6 Libramiento Norte Carretera, Irapuato-León, Irapuato 36821, Guanajuato, Mexico; [email protected] 2 Metabolic Engineering Group, Unidad de Genómica Avanzada, Laboratorio Nacional de Genómica para la Biodiversidad, Cinvestav Sede Irapuato, Km. 9.6 Libramiento Norte Carretera, Irapuato-León, Irapuato 36821, Guanajuato, Mexico; [email protected] 3 Botanical Research Institute of Texas (BRIT), Fort Worth, TX 76107-3400, USA; [email protected] 4 Laboratory of Plant Cell and Developmental Biology, Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia; [email protected] 5 Institute of Genomics for Crop Abiotic Stress Tolerance, Department of Plant and Soil Science, Texas Tech University, Lubbock, TX 79409, USA * Correspondence: [email protected] Received: 27 October 2020; Accepted: 26 November 2020; Published: 4 December 2020 Abstract: Ferns are a representative clade in plant evolution although underestimated in the genomic era. Ceratopteris richardii is an emergent model for developmental processes in ferns, yet a complete scheme of the different growth stages is necessary. Here, we present a developmental analysis, at the tissue and cellular levels, of the first shoot-borne root of Ceratopteris. -
Morphological Description of Plants: New Perspectives in Development and Evolution
® International Journal of Plant Developmental Biology ©2010 Global Science Books Morphological Description of Plants: New Perspectives in Development and Evolution 1* 2 Emilio Cervantes • Juana G . de Diego 1 IRNASA-CSIC. Apartado 257. 37080. Salamanca. Spain 2 Dept Bioquímica y Biología Molecular. Campus Miguel de Unamuno. Universidad de Salamanca. Spain Corresponding author : * [email protected] ABSTRACT The morphological description of plants has been fundamental in the history of botany and provided the keys for taxonomy. Nevertheless, in biology, a discipline governed by the interest in function and based on reductionist approaches, the analysis of forms has been relegated to second place. Plants contain organs and structures that resemble geometrical forms. Plant ontogeny may be seen as a sequence of growth processes including periods of continuous growth with modification that stop at crucial points often represented by structures of remarkable similarity to geometrical figures. Instead of the tradition in developmental studies giving more importance to animal models, we propose that the modular type of plant development may serve to remark conceptual aspects in that may be useful in studies with animals and contribute to original views of evolution. _____________________________________________________________________________________________________________ Keywords: concepts, description, geometry, structure INTRODUCTION: PLANTS OFFER NEW reflects a more general situation in Biology, a discipline APPROACHES TO DEVELOPMENT that has matured from the experimental protocols and views of biochemistry, where the predominant role of experimen- The study of development is today a major biological disci- tation has contributed to a decline in basic aspects that need pline. Although it was traditionally more focused in animal to be more descriptive, such as those related with mor- systems, increased emphasis in plant development may phology. -
Phyllotaxis: a Remarkable Example of Developmental Canalization in Plants Christophe Godin, Christophe Golé, Stéphane Douady
Phyllotaxis: a remarkable example of developmental canalization in plants Christophe Godin, Christophe Golé, Stéphane Douady To cite this version: Christophe Godin, Christophe Golé, Stéphane Douady. Phyllotaxis: a remarkable example of devel- opmental canalization in plants. 2019. hal-02370969 HAL Id: hal-02370969 https://hal.archives-ouvertes.fr/hal-02370969 Preprint submitted on 19 Nov 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Phyllotaxis: a remarkable example of developmental canalization in plants Christophe Godin, Christophe Gol´e,St´ephaneDouady September 2019 Abstract Why living forms develop in a relatively robust manner, despite various sources of internal or external variability, is a fundamental question in developmental biology. Part of the answer relies on the notion of developmental constraints: at any stage of ontogenenesis, morphogenetic processes are constrained to operate within the context of the current organism being built, which is thought to bias or to limit phenotype variability. One universal aspect of this context is the shape of the organism itself that progressively channels the development of the organism toward its final shape. Here, we illustrate this notion with plants, where conspicuous patterns are formed by the lateral organs produced by apical meristems. -
A Genetic Framework for Regulation and Seasonal Adaptation of Shoot Architecture in Hybrid Aspen
A genetic framework for regulation and seasonal adaptation of shoot architecture in hybrid aspen Jay P. Mauryaa,b, Pal C. Miskolczia, Sanatkumar Mishraa, Rajesh Kumar Singha, and Rishikesh P. Bhaleraoa,1 aUmeå Plant Science Centre, Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, SE-901 87 Umeå, Sweden; and bDepartment of Botany, Institute of Science, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India Edited by Ronald R. Sederoff, North Carolina State University, Raleigh, NC, and approved April 14, 2020 (received for review March 14, 2020) Shoot architecture is critical for optimizing plant adaptation and time–related transcription factor RAV1 has been validated in productivity. In contrast with annuals, branching in perennials branching in trees (17–19). However, information on branching native to temperate and boreal regions must be coordinated with control in perennials is fragmented, and there is a significant gap seasonal growth cycles. How branching is coordinated with in our knowledge of how branching is controlled and integrated seasonal growth is poorly understood. We identified key compo- with seasonal growth cycles in perennial trees (20). Therefore, nents of the genetic network that controls branching and its using functional genetic approaches, we elucidated the genetic regulation by seasonal cues in the model tree hybrid aspen. network that mediates control of branching and its regulation by Our results demonstrate that branching and its control by sea- seasonal cues in the model tree hybrid aspen. These studies re- sonal cues is mediated by mutually antagonistic action of aspen veal the key role played by the mutually antagonistic action of orthologs of the flowering regulators TERMINAL FLOWER 1 LAP1 and TFL1 in mediating control of branching and its re- (TFL1)andAPETALA1 (LIKE APETALA 1/LAP1). -
Plant Development Series Editor Paul M
VOLUME NINETY ONE CURRENT TOPICS IN DEVELOPMENTAL BIOLOGY Plant Development Series Editor Paul M. Wassarman Department of Developmental and Regenerative Biology Mount Sinai School of Medicine New York, NY 10029-6574 USA Olivier Pourquié Institut de Génétique et de Biologie Cellulaire et Moléculaire (IGBMC) Inserm U964, CNRS (UMR 7104) Université de Strasbourg Illkirch France Editorial Board Blanche Capel Duke University Medical Center Durham, NC, USA B. Denis Duboule Department of Zoology and Animal Biology NCCR ‘Frontiers in Genetics’ Geneva, Switzerland Anne Ephrussi European Molecular Biology Laboratory Heidelberg, Germany Janet Heasman Cincinnati Children’s Hospital Medical Center Department of Pediatrics Cincinnati, OH, USA Julian Lewis Vertebrate Development Laboratory Cancer Research UK London Research Institute London WC2A 3PX, UK Yoshiki Sasai Director of the Neurogenesis and Organogenesis Group RIKEN Center for Developmental Biology Chuo, Japan Philippe Soriano Department of Developmental and Regenerative Biology Mount Sinai Medical School New York, USA Cliff Tabin Harvard Medical School Department of Genetics Boston, MA, USA Founding Editors A. A. Moscona Alberto Monroy VOLUME NINETY ONE CURRENT TOPICS IN DEVELOPMENTAL BIOLOGY Plant Development Edited by MARJA C. P. TIMMERMANS Cold Spring Harbor Laboratory Cold Spring Harbor New York, USA AMSTERDAM • BOSTON • HEIDELBERG • LONDON NEW YORK • OXFORD • PARIS • SAN DIEGO SAN FRANCISCO • SINGAPORE • SYDNEY • TOKYO Academic Press is an imprint of Elsevier Academic Press is an imprint of Elsevier 525 B Street, Suite 1900, San Diego, CA 92101-4495, USA 30 Corporate Drive, Suite 400, Burlington, MA 01803, USA 32, Jamestown Road, London NW1 7BY, UK Linacre House, Jordan Hill, Oxford OX2 8DP, UK First edition 2010 Copyright Ó 2010 Elsevier Inc. -
The Interaction of Cytokinin and Strigolactone in Controlling Shoot Branching in Arabidopsis Thaliana
The Interaction of Cytokinin and Strigolactone in controlling Shoot Branching in Arabidopsis thaliana By Neelam Chaudhary Imperial College London Department of Life Sciences November 2013 A thesis submitted for the degree of Doctor of Philosophy and the Diploma of Imperial College London 1 For my Father (Late) and Mother They struggled hard to strengthen my faith in Almighty Allah and supported me to fulfil my dreams and to achieve my goals through their constant unconditional love, encouragement and prayers. For Scientists especially Life Scientists They spare time learning new ways to understand and solve problems in hopes of paving a better future for newer generations. They are more dedicated to making solid achievements than in running after swift but synthetic happiness. 2 ABSTRACT Shoot branching is regulated by auxin, cytokinin (CK) and strigolactone (SL). Cytokinin, being the only promoter of shoot branching, is antagonistic in function to auxin and strigolactone, which inhibit shoot branching. There is a close relationship between auxin and strigolactone, mediating each other to suppress shoot branching. Strigolactone reduces auxin transport from the buds, thus arresting bud outgrowth. On the other hand, auxin increases strigolactone production to control apical dominance. Antagonistic interaction between auxin and cytokinin has been reported as auxin inhibits lateral bud outgrowth by limiting CK supply to axillary buds. Previously, it has been found that levels of tZ-type CKs are extremely low in xylem sap of strigolactone mutants of Arabidopsis and pea.The current research aimed to explore the interaction between cytokinin and strigolactone, especially the regulatory mechanisms behind these low cytokinin levels. -
Florigen Governs Shoot Regeneration
Florigen Governs Shoot Regeneration Yaarit Kutsher Agricultural Research Organization Michal Fisler Agricultural Research Organization Adi DORON-FAIGENBOIM Agricultural Research Organization Moshe Reuveni ( [email protected] ) Agricultural Research Organization Research Article Keywords: reproductive stage (owering), protocols of shoot regeneration in plants, tobacco origen mRNA Posted Date: April 30th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-450479/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/16 Abstract It is widely known that during the reproductive stage (owering), plants do not root well. Most protocols of shoot regeneration in plants utilize juvenile tissue. Adding these two realities together encouraged us to study the role of origen in shoot regeneration. Mature tobacco tissue that expresses the endogenous tobacco origen mRNA regenerates poorly, while juvenile tissue that does not express the origen regenerates shoots well. Inhibition of Nitric Oxide (NO) synthesis reduced shoot regeneration as well as promoted owering and increased tobacco origen level. In contrast, the addition of NO (by way of NO donor) to the tissue increased regeneration, delayed owering, reduced tobacco origen mRNA. Ectopic expression of origen genes in tobacco or tomato decreased regeneration capacity signicantly. Overexpression pear PcFT2 gene increased regeneration capacity. During regeneration, origen mRNA was not changed. We conclude that origen presence in mature tobacco leaves reduces roots and shoots regeneration and is the possible reason for the age-related decrease in regeneration capacity. Introduction Plant regeneration by rebuilding new organs (organogenesis) results from new organ formation through dedifferentiation of differentiated plant cells and reorganization of cell division to create new organ meristems and new vascular connection between the explant and the newly regenerating organ 1,2. -
Root Development and Stress Tolerance in Rice: the Key to Improving Stress Tolerance Without Yield Penalties
International Journal of Molecular Sciences Review Root Development and Stress Tolerance in rice: The Key to Improving Stress Tolerance without Yield Penalties Deok Hyun Seo 1, Subhin Seomun 1, Yang Do Choi 2 and Geupil Jang 1,* 1 School of Biological Sciences and Technology, Chonnam National University, Gwangju 61186, Korea; [email protected] (D.H.S.); [email protected] (S.S.) 2 The National Academy of Sciences, Seoul 06579, Korea; [email protected] * Correspondence: [email protected] Received: 12 February 2020; Accepted: 4 March 2020; Published: 6 March 2020 Abstract: Roots anchor plants and take up water and nutrients from the soil; therefore, root development strongly affects plant growth and productivity. Moreover, increasing evidence indicates that root development is deeply involved in plant tolerance to abiotic stresses such as drought and salinity. These findings suggest that modulating root growth and development provides a potentially useful approach to improve plant abiotic stress tolerance. Such targeted approaches may avoid the yield penalties that result from growth–defense trade-offs produced by global induction of defenses against abiotic stresses. This review summarizes the developmental mechanisms underlying root development and discusses recent studies about modulation of root growth and stress tolerance in rice. Keywords: root; auxin; abiotic stress; tolerance; rice 1. Introduction Abiotic stress, including drought, low or high temperature, and salinity, seriously affects growth and productivity of plants [1]. Furthermore, global climate change may be increasing the frequency and severity of abiotic stress, thus threatening food production around the world [2]. In nature, plants are continuously exposed to different abiotic stresses and have evolved a variety of defense mechanisms to survive these abiotic stresses.