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Phyllotaxis Turns Over a New Leaf—A New Hypothesis
Phyllotaxis describes the periodic arrangement of plant organs most conspicuously floral. Oscillators generally underlie periodic phenomena. A hypothetical algorithm generates phyllotaxis regulated by the Hechtian growth oscillator of the stem apical meristem (SAM) protoderm. The oscillator integrat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037126/ https://www.ncbi.nlm.nih.gov/pubmed/32050457 http://dx.doi.org/10.3390/ijms21031145 |
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author | Lamport, Derek T. A. Tan, Li Held, Michael Kieliszewski, Marcia J. |
author_facet | Lamport, Derek T. A. Tan, Li Held, Michael Kieliszewski, Marcia J. |
author_sort | Lamport, Derek T. A. |
collection | PubMed |
description | Phyllotaxis describes the periodic arrangement of plant organs most conspicuously floral. Oscillators generally underlie periodic phenomena. A hypothetical algorithm generates phyllotaxis regulated by the Hechtian growth oscillator of the stem apical meristem (SAM) protoderm. The oscillator integrates biochemical and mechanical force that regulate morphogenetic gradients of three ionic species, auxin, protons and Ca(2+). Hechtian adhesion between cell wall and plasma membrane transduces wall stress that opens Ca(2+) channels and reorients auxin efflux “PIN” proteins; they control the auxin-activated proton pump that dissociates Ca(2+) bound by periplasmic arabinogalactan proteins (AGP-Ca(2+)) hence the source of cytosolic Ca(2+) waves that activate exocytosis of wall precursors, AGPs and PIN proteins essential for morphogenesis. This novel approach identifies the critical determinants of an algorithm that generates phyllotaxis spiral and Fibonaccian symmetry: these determinants in order of their relative contribution are: (1) size of the apical meristem and the AGP-Ca(2+) capacitor; (2) proton pump activity; (3) auxin efflux proteins; (4) Ca(2+) channel activity; (5) Hechtian adhesion that mediates the cell wall stress vector. Arguably, AGPs and the AGP-Ca(2+) capacitor plays a decisive role in phyllotaxis periodicity and its evolutionary origins. |
format | Online Article Text |
id | pubmed-7037126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70371262020-03-11 Phyllotaxis Turns Over a New Leaf—A New Hypothesis Lamport, Derek T. A. Tan, Li Held, Michael Kieliszewski, Marcia J. Int J Mol Sci Review Phyllotaxis describes the periodic arrangement of plant organs most conspicuously floral. Oscillators generally underlie periodic phenomena. A hypothetical algorithm generates phyllotaxis regulated by the Hechtian growth oscillator of the stem apical meristem (SAM) protoderm. The oscillator integrates biochemical and mechanical force that regulate morphogenetic gradients of three ionic species, auxin, protons and Ca(2+). Hechtian adhesion between cell wall and plasma membrane transduces wall stress that opens Ca(2+) channels and reorients auxin efflux “PIN” proteins; they control the auxin-activated proton pump that dissociates Ca(2+) bound by periplasmic arabinogalactan proteins (AGP-Ca(2+)) hence the source of cytosolic Ca(2+) waves that activate exocytosis of wall precursors, AGPs and PIN proteins essential for morphogenesis. This novel approach identifies the critical determinants of an algorithm that generates phyllotaxis spiral and Fibonaccian symmetry: these determinants in order of their relative contribution are: (1) size of the apical meristem and the AGP-Ca(2+) capacitor; (2) proton pump activity; (3) auxin efflux proteins; (4) Ca(2+) channel activity; (5) Hechtian adhesion that mediates the cell wall stress vector. Arguably, AGPs and the AGP-Ca(2+) capacitor plays a decisive role in phyllotaxis periodicity and its evolutionary origins. MDPI 2020-02-09 /pmc/articles/PMC7037126/ /pubmed/32050457 http://dx.doi.org/10.3390/ijms21031145 Text en © 2020 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Lamport, Derek T. A. Tan, Li Held, Michael Kieliszewski, Marcia J. Phyllotaxis Turns Over a New Leaf—A New Hypothesis |
title | Phyllotaxis Turns Over a New Leaf—A New Hypothesis |
title_full | Phyllotaxis Turns Over a New Leaf—A New Hypothesis |
title_fullStr | Phyllotaxis Turns Over a New Leaf—A New Hypothesis |
title_full_unstemmed | Phyllotaxis Turns Over a New Leaf—A New Hypothesis |
title_short | Phyllotaxis Turns Over a New Leaf—A New Hypothesis |
title_sort | phyllotaxis turns over a new leaf—a new hypothesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037126/ https://www.ncbi.nlm.nih.gov/pubmed/32050457 http://dx.doi.org/10.3390/ijms21031145 |
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