Primary wall cellulose synthase regulates shoot apical meristem mechanics and growth
How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure, and are surrounded by a rigid yet flexible cell wall, which is the primary determinant o...
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| Published in | Development (Cambridge) Vol. 146; no. 10; pp. 1 - 11 |
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| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
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England
Company of Biologists
24.05.2019
The Company of Biologists Ltd |
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| Abstract | How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure, and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding genetic and biophysical regulation of morphogenesis, direct studies on cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we take advantage of mutants of three primary cellulose synthase (CESA) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem. |
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| AbstractList | How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure, and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding genetic and biophysical regulation of morphogenesis, direct studies on cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we take advantage of mutants of three primary cellulose synthase (CESA) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem. How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding the genetic and biophysical regulation of morphogenesis, direct studies of cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we took advantage of mutants of three primary cellulose synthase ( ) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem. How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding the genetic and biophysical regulation of morphogenesis, direct studies of cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we took advantage of mutants of three primary cellulose synthase (CESA) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem.How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding the genetic and biophysical regulation of morphogenesis, direct studies of cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we took advantage of mutants of three primary cellulose synthase (CESA) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem. How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding the genetic and biophysical regulation of morphogenesis, direct studies of cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we took advantage of mutants of three primary cellulose synthase ( CESA ) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem. Highlighted Article: An interdisciplinary approach reveals that the CELLULOSE SYNTHASE complex influences both physical and biological processes at the shoot apical meristem. How organisms attain their specific shapes and modify their growth patterns in response to environmental and chemical signals has been the subject of many investigations. Plant cells are at high turgor pressure and are surrounded by a rigid yet flexible cell wall, which is the primary determinant of plant growth and morphogenesis. Cellulose microfibrils, synthesized by plasma membrane-localized cellulose synthase complexes, are major tension-bearing components of the cell wall that mediate directional growth. Despite advances in understanding the genetic and biophysical regulation of morphogenesis, direct studies of cellulose biosynthesis and its impact on morphogenesis of different cell and tissue types are largely lacking. In this study, we took advantage of mutants of three primary cellulose synthase (CESA) genes that are involved in primary wall cellulose synthesis. Using field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed to understand how the primary wall CESA complex acts during shoot apical meristem development. Our results indicate that cellulose biosynthesis impacts the mechanics and growth of the shoot apical meristem. |
| Author | Peaucelle, Alexis Wasteneys, Geoffrey O. Schuster, Christoph Meyerowitz, Elliot M. Fujita, Miki Sampathkumar, Arun Persson, Staffan |
| AuthorAffiliation | 5 School of Biosciences, University of Melbourne , Parkville, VIC 3010 , Australia 3 Department of Botany , University of British Columbia , 6270 University Boulevard, Vancouver V6T 1Z4, Canada 4 Sainsbury Laboratory , University of Cambridge , Cambridge CB2 1LR , UK 6 Howard Hughes Medical Institute and Division of Biology and Biological Engineering, 1200 East California Boulevard, Pasadena, CA 91125 , USA 1 Max Planck Institute of Molecular Plant Physiology , Am Mühlenberg 1, 14476 Potsdam-Golm , Germany 2 Institut Jean-Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris-Saclay, 78000, Versailles , France |
| AuthorAffiliation_xml | – name: 3 Department of Botany , University of British Columbia , 6270 University Boulevard, Vancouver V6T 1Z4, Canada – name: 4 Sainsbury Laboratory , University of Cambridge , Cambridge CB2 1LR , UK – name: 5 School of Biosciences, University of Melbourne , Parkville, VIC 3010 , Australia – name: 6 Howard Hughes Medical Institute and Division of Biology and Biological Engineering, 1200 East California Boulevard, Pasadena, CA 91125 , USA – name: 1 Max Planck Institute of Molecular Plant Physiology , Am Mühlenberg 1, 14476 Potsdam-Golm , Germany – name: 2 Institut Jean-Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris-Saclay, 78000, Versailles , France |
| Author_xml | – sequence: 1 givenname: Arun surname: Sampathkumar fullname: Sampathkumar, Arun organization: Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476 Potsdam-Golm, Germany – sequence: 2 givenname: Alexis surname: Peaucelle fullname: Peaucelle, Alexis organization: Institut Jean-Pierre Bourgin, UMR1318, Institut National pour la Recherche Agronomique-AgroParisTech, Saclay Plant Science, Route de St-Cyr, Versailles 78026, France – sequence: 3 givenname: Miki surname: Fujita fullname: Fujita, Miki organization: Department of Botany, University of British Columbia, 6270 University Blvd. Vancouver, Canada – sequence: 4 givenname: Christoph surname: Schuster fullname: Schuster, Christoph organization: Sainsbury Laboratory, University of Cambridge, CB2 1LR Cambridge, UK – sequence: 5 givenname: Staffan surname: Persson fullname: Persson, Staffan organization: School of Biosciences, University of Melbourne, Parkville, Vic 3010, Australia – sequence: 6 givenname: Geoffrey O. surname: Wasteneys fullname: Wasteneys, Geoffrey O. organization: Department of Botany, University of British Columbia, 6270 University Blvd. Vancouver, Canada – sequence: 7 givenname: Elliot M. surname: Meyerowitz fullname: Meyerowitz, Elliot M. organization: Howard Hughes Medical Institute and Division of Biology and Biological Engineering, 1200 East California Boulevard, Pasadena, CA 91125, USA |
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| Keywords | Morphogenesis Mechanics Cell growth Microtubules Cell wall Cellulose |
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| Title | Primary wall cellulose synthase regulates shoot apical meristem mechanics and growth |
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