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Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis

Unlike animal cells, plant cells do not possess centrosomes that serve as microtubule organizing centers; how microtubule arrays are organized throughout plant morphogenesis remains poorly understood. We report here that Arabidopsis INCREASED PETAL GROWTH ANISOTROPY 1 (IPGA1), a previously uncharact...

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Autores principales: Yang, Yanqiu, Chen, Binqinq, Dang, Xie, Zhu, Lilan, Rao, Jinqiu, Ren, Huibo, Lin, Chentao, Qin, Yuan, Lin, Deshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6793458/
https://www.ncbi.nlm.nih.gov/pubmed/31198941
http://dx.doi.org/10.1093/jxb/erz284
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author Yang, Yanqiu
Chen, Binqinq
Dang, Xie
Zhu, Lilan
Rao, Jinqiu
Ren, Huibo
Lin, Chentao
Qin, Yuan
Lin, Deshu
author_facet Yang, Yanqiu
Chen, Binqinq
Dang, Xie
Zhu, Lilan
Rao, Jinqiu
Ren, Huibo
Lin, Chentao
Qin, Yuan
Lin, Deshu
author_sort Yang, Yanqiu
collection PubMed
description Unlike animal cells, plant cells do not possess centrosomes that serve as microtubule organizing centers; how microtubule arrays are organized throughout plant morphogenesis remains poorly understood. We report here that Arabidopsis INCREASED PETAL GROWTH ANISOTROPY 1 (IPGA1), a previously uncharacterized microtubule-associated protein, regulates petal growth and shape by affecting cortical microtubule organization. Through a genetic screen, we showed that IPGA1 loss-of-function mutants displayed a phenotype of longer and narrower petals, as well as increased anisotropic cell expansion of the petal epidermis in the late phases of flower development. Map-based cloning studies revealed that IPGA1 encodes a previously uncharacterized protein that colocalizes with and directly binds to microtubules. IPGA1 plays a negative role in the organization of cortical microtubules into parallel arrays oriented perpendicular to the axis of cell elongation, with the ipga1-1 mutant displaying increased microtubule ordering in petal abaxial epidermal cells. The IPGA1 family is conserved among land plants and its homologs may have evolved to regulate microtubule organization. Taken together, our findings identify IPGA1 as a novel microtubule-associated protein and provide significant insights into IPGA1-mediated microtubule organization and petal growth anisotropy.
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spelling pubmed-67934582019-10-18 Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis Yang, Yanqiu Chen, Binqinq Dang, Xie Zhu, Lilan Rao, Jinqiu Ren, Huibo Lin, Chentao Qin, Yuan Lin, Deshu J Exp Bot Research Papers Unlike animal cells, plant cells do not possess centrosomes that serve as microtubule organizing centers; how microtubule arrays are organized throughout plant morphogenesis remains poorly understood. We report here that Arabidopsis INCREASED PETAL GROWTH ANISOTROPY 1 (IPGA1), a previously uncharacterized microtubule-associated protein, regulates petal growth and shape by affecting cortical microtubule organization. Through a genetic screen, we showed that IPGA1 loss-of-function mutants displayed a phenotype of longer and narrower petals, as well as increased anisotropic cell expansion of the petal epidermis in the late phases of flower development. Map-based cloning studies revealed that IPGA1 encodes a previously uncharacterized protein that colocalizes with and directly binds to microtubules. IPGA1 plays a negative role in the organization of cortical microtubules into parallel arrays oriented perpendicular to the axis of cell elongation, with the ipga1-1 mutant displaying increased microtubule ordering in petal abaxial epidermal cells. The IPGA1 family is conserved among land plants and its homologs may have evolved to regulate microtubule organization. Taken together, our findings identify IPGA1 as a novel microtubule-associated protein and provide significant insights into IPGA1-mediated microtubule organization and petal growth anisotropy. Oxford University Press 2019-10-01 2019-06-13 /pmc/articles/PMC6793458/ /pubmed/31198941 http://dx.doi.org/10.1093/jxb/erz284 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Papers
Yang, Yanqiu
Chen, Binqinq
Dang, Xie
Zhu, Lilan
Rao, Jinqiu
Ren, Huibo
Lin, Chentao
Qin, Yuan
Lin, Deshu
Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
title Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
title_full Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
title_fullStr Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
title_full_unstemmed Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
title_short Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
title_sort arabidopsis ipga1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6793458/
https://www.ncbi.nlm.nih.gov/pubmed/31198941
http://dx.doi.org/10.1093/jxb/erz284
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