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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...

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Autores principales: Chang, Jiang, Xu, Zhijing, Li, Meng, Yang, Meina, Qin, Haiyang, Yang, Jie, Wu, Shuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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