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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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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. |
format | Online Article Text |
id | pubmed-6793458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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