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GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport
Plant cell expands via a tip growth or diffuse growth mode. In plants, RabA is the largest group of Rab GTPases that regulate vesicle trafficking. The functions of RabA protein in modulating polarized expansion in tip growth cells have been demonstrated. However, whether and how RabA protein functio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449706/ https://www.ncbi.nlm.nih.gov/pubmed/36271510 http://dx.doi.org/10.26508/lsa.202201450 |
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author | Shang, Xiaoguang Duan, Yujia Zhao, Meiyue Zhu, Lijie Liu, Hanqiao He, Qingfei Yu, Yujia Li, Weixi Amjid, Muhammad Waqas Ruan, Yong-Ling Guo, Wangzhen |
author_facet | Shang, Xiaoguang Duan, Yujia Zhao, Meiyue Zhu, Lijie Liu, Hanqiao He, Qingfei Yu, Yujia Li, Weixi Amjid, Muhammad Waqas Ruan, Yong-Ling Guo, Wangzhen |
author_sort | Shang, Xiaoguang |
collection | PubMed |
description | Plant cell expands via a tip growth or diffuse growth mode. In plants, RabA is the largest group of Rab GTPases that regulate vesicle trafficking. The functions of RabA protein in modulating polarized expansion in tip growth cells have been demonstrated. However, whether and how RabA protein functions in diffuse growth plant cells have never been explored. Here, we addressed this question by examining the role of GhRabA4c in cotton fibers. GhRabA4c was preferentially expressed in elongating fibers with its protein localized to endoplasmic reticulum and Golgi apparatus. Over- and down-expression of GhRabA4c in cotton lead to longer and shorter fibers, respectively. GhRabA4c interacted with GhACT4 to promote the assembly of actin filament to facilitate vesicle transport for cell wall synthesis. Consistently, GhRabA4c-overexpressed fibers exhibited increased content of wall components and the transcript levels of the genes responsible for the synthesis of cell wall materials. We further identified two MYB proteins that directly regulate the transcription of GhRabA4c. Collectively, our data showed that GhRabA4c promotes diffused cell expansion by supporting vesicle trafficking and cell wall synthesis. |
format | Online Article Text |
id | pubmed-9449706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-94497062022-09-08 GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport Shang, Xiaoguang Duan, Yujia Zhao, Meiyue Zhu, Lijie Liu, Hanqiao He, Qingfei Yu, Yujia Li, Weixi Amjid, Muhammad Waqas Ruan, Yong-Ling Guo, Wangzhen Life Sci Alliance Research Articles Plant cell expands via a tip growth or diffuse growth mode. In plants, RabA is the largest group of Rab GTPases that regulate vesicle trafficking. The functions of RabA protein in modulating polarized expansion in tip growth cells have been demonstrated. However, whether and how RabA protein functions in diffuse growth plant cells have never been explored. Here, we addressed this question by examining the role of GhRabA4c in cotton fibers. GhRabA4c was preferentially expressed in elongating fibers with its protein localized to endoplasmic reticulum and Golgi apparatus. Over- and down-expression of GhRabA4c in cotton lead to longer and shorter fibers, respectively. GhRabA4c interacted with GhACT4 to promote the assembly of actin filament to facilitate vesicle transport for cell wall synthesis. Consistently, GhRabA4c-overexpressed fibers exhibited increased content of wall components and the transcript levels of the genes responsible for the synthesis of cell wall materials. We further identified two MYB proteins that directly regulate the transcription of GhRabA4c. Collectively, our data showed that GhRabA4c promotes diffused cell expansion by supporting vesicle trafficking and cell wall synthesis. Life Science Alliance LLC 2022-09-06 /pmc/articles/PMC9449706/ /pubmed/36271510 http://dx.doi.org/10.26508/lsa.202201450 Text en © 2022 Shang et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Shang, Xiaoguang Duan, Yujia Zhao, Meiyue Zhu, Lijie Liu, Hanqiao He, Qingfei Yu, Yujia Li, Weixi Amjid, Muhammad Waqas Ruan, Yong-Ling Guo, Wangzhen GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
title | GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
title_full | GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
title_fullStr | GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
title_full_unstemmed | GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
title_short | GhRabA4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
title_sort | ghraba4c coordinates cell elongation via regulating actin filament–dependent vesicle transport |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449706/ https://www.ncbi.nlm.nih.gov/pubmed/36271510 http://dx.doi.org/10.26508/lsa.202201450 |
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