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Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato
Plant trichomes originate from epidermal cell, forming protective structure from abiotic and biotic stresses. Different from the unicellular trichome in Arabidopsis, tomato trichomes are multicellular structure and can be classified into seven different types based on cell number, shape and the pres...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812842/ https://www.ncbi.nlm.nih.gov/pubmed/31584936 http://dx.doi.org/10.1371/journal.pgen.1008438 |
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author | Chang, Jiang Xu, Zhijing Li, Meng Yang, Meina Qin, Haiyang Yang, Jie Wu, Shuang |
author_facet | Chang, Jiang Xu, Zhijing Li, Meng Yang, Meina Qin, Haiyang Yang, Jie Wu, Shuang |
author_sort | Chang, Jiang |
collection | PubMed |
description | Plant trichomes originate from epidermal cell, forming protective structure from abiotic and biotic stresses. Different from the unicellular trichome in Arabidopsis, tomato trichomes are multicellular structure and can be classified into seven different types based on cell number, shape and the presence of glandular cells. Despite the importance of tomato trichomes in insect resistance, our understanding of the tomato trichome morphogenesis remains elusive. In this study, we quantitatively analyzed morphological traits of trichomes in tomato and further performed live imaging of cytoskeletons in stably transformed lines with actin and microtubule markers. At different developmental stages, two types of cytoskeletons exhibited distinct patterns in different trichome cells, ranging from transverse, spiral to longitudinal. This gradual transition of actin filament angle from basal to top cells could correlate with the spatial expansion mode in different cells. Further genetic screen for aberrant trichome morphology led to the discovery of a number of independent mutations in SCAR/WAVE and ARP2/3 complex, which resulted in actin bundling and distorted trichomes. Disruption of microtubules caused isotropic expansion while abolished actin filaments entirely inhibited axial extension of trichomes, indicating that microtubules and actin filaments may control distinct aspects of trichome cell expansion. Our results shed light on the roles of cytoskeletons in the formation of multicellular structure of tomato trichomes. |
format | Online Article Text |
id | pubmed-6812842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68128422019-11-02 Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato Chang, Jiang Xu, Zhijing Li, Meng Yang, Meina Qin, Haiyang Yang, Jie Wu, Shuang PLoS Genet Research Article Plant trichomes originate from epidermal cell, forming protective structure from abiotic and biotic stresses. Different from the unicellular trichome in Arabidopsis, tomato trichomes are multicellular structure and can be classified into seven different types based on cell number, shape and the presence of glandular cells. Despite the importance of tomato trichomes in insect resistance, our understanding of the tomato trichome morphogenesis remains elusive. In this study, we quantitatively analyzed morphological traits of trichomes in tomato and further performed live imaging of cytoskeletons in stably transformed lines with actin and microtubule markers. At different developmental stages, two types of cytoskeletons exhibited distinct patterns in different trichome cells, ranging from transverse, spiral to longitudinal. This gradual transition of actin filament angle from basal to top cells could correlate with the spatial expansion mode in different cells. Further genetic screen for aberrant trichome morphology led to the discovery of a number of independent mutations in SCAR/WAVE and ARP2/3 complex, which resulted in actin bundling and distorted trichomes. Disruption of microtubules caused isotropic expansion while abolished actin filaments entirely inhibited axial extension of trichomes, indicating that microtubules and actin filaments may control distinct aspects of trichome cell expansion. Our results shed light on the roles of cytoskeletons in the formation of multicellular structure of tomato trichomes. Public Library of Science 2019-10-04 /pmc/articles/PMC6812842/ /pubmed/31584936 http://dx.doi.org/10.1371/journal.pgen.1008438 Text en © 2019 Chang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chang, Jiang Xu, Zhijing Li, Meng Yang, Meina Qin, Haiyang Yang, Jie Wu, Shuang Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
title | Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
title_full | Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
title_fullStr | Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
title_full_unstemmed | Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
title_short | Spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
title_sort | spatiotemporal cytoskeleton organizations determine morphogenesis of multicellular trichomes in tomato |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812842/ https://www.ncbi.nlm.nih.gov/pubmed/31584936 http://dx.doi.org/10.1371/journal.pgen.1008438 |
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