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OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis

The actin cytoskeleton is crucial for plant morphogenesis, and organization of actin filaments (AF) is dynamically regulated by actin-binding proteins. However, the roles of actin-binding proteins, particularly type II formins, in this process remain poorly understood in plants. Here, we report that...

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Autores principales: Chang, Shuwei, Ren, Zhanhong, Liu, Chang, Du, Pingzhou, Li, Jingbin, Liu, Zengyu, Zhang, Fengli, Hou, Haili, Shi, Jianxin, Liang, Wanqi, Yang, Litao, Ren, Haiyun, Zhang, Dabing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706662/
https://www.ncbi.nlm.nih.gov/pubmed/34948047
http://dx.doi.org/10.3390/ijms222413250
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author Chang, Shuwei
Ren, Zhanhong
Liu, Chang
Du, Pingzhou
Li, Jingbin
Liu, Zengyu
Zhang, Fengli
Hou, Haili
Shi, Jianxin
Liang, Wanqi
Yang, Litao
Ren, Haiyun
Zhang, Dabing
author_facet Chang, Shuwei
Ren, Zhanhong
Liu, Chang
Du, Pingzhou
Li, Jingbin
Liu, Zengyu
Zhang, Fengli
Hou, Haili
Shi, Jianxin
Liang, Wanqi
Yang, Litao
Ren, Haiyun
Zhang, Dabing
author_sort Chang, Shuwei
collection PubMed
description The actin cytoskeleton is crucial for plant morphogenesis, and organization of actin filaments (AF) is dynamically regulated by actin-binding proteins. However, the roles of actin-binding proteins, particularly type II formins, in this process remain poorly understood in plants. Here, we report that a type II formin in rice, Oryza sativa formin homolog 3 (OsFH3), acts as a major player to modulate AF dynamics and contributes to rice morphogenesis. osfh3 mutants were semi-dwarf with reduced size of seeds and unchanged responses to light or gravity compared with mutants of osfh5, another type II formin in rice. osfh3 osfh5 mutants were dwarf with more severe developmental defectiveness. Recombinant OsFH3 could nucleate actin, promote AF bundling, and cap the barbed end of AF to prevent elongation and depolymerization, but in the absence of profilin, OsFH3 could inhibit AF elongation. Different from other reported type II formins, OsFH3 could bind, but not bundle, microtubules directly. Furthermore, its N-terminal phosphatase and tensin homolog domain played a key role in modulating OsFH3 localization at intersections of AF and punctate structures of microtubules, which differed from other reported plant formins. Our results, thus, provide insights into the biological function of type II formins in modulating plant morphology by acting on AF dynamics.
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spelling pubmed-87066622021-12-25 OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis Chang, Shuwei Ren, Zhanhong Liu, Chang Du, Pingzhou Li, Jingbin Liu, Zengyu Zhang, Fengli Hou, Haili Shi, Jianxin Liang, Wanqi Yang, Litao Ren, Haiyun Zhang, Dabing Int J Mol Sci Article The actin cytoskeleton is crucial for plant morphogenesis, and organization of actin filaments (AF) is dynamically regulated by actin-binding proteins. However, the roles of actin-binding proteins, particularly type II formins, in this process remain poorly understood in plants. Here, we report that a type II formin in rice, Oryza sativa formin homolog 3 (OsFH3), acts as a major player to modulate AF dynamics and contributes to rice morphogenesis. osfh3 mutants were semi-dwarf with reduced size of seeds and unchanged responses to light or gravity compared with mutants of osfh5, another type II formin in rice. osfh3 osfh5 mutants were dwarf with more severe developmental defectiveness. Recombinant OsFH3 could nucleate actin, promote AF bundling, and cap the barbed end of AF to prevent elongation and depolymerization, but in the absence of profilin, OsFH3 could inhibit AF elongation. Different from other reported type II formins, OsFH3 could bind, but not bundle, microtubules directly. Furthermore, its N-terminal phosphatase and tensin homolog domain played a key role in modulating OsFH3 localization at intersections of AF and punctate structures of microtubules, which differed from other reported plant formins. Our results, thus, provide insights into the biological function of type II formins in modulating plant morphology by acting on AF dynamics. MDPI 2021-12-09 /pmc/articles/PMC8706662/ /pubmed/34948047 http://dx.doi.org/10.3390/ijms222413250 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chang, Shuwei
Ren, Zhanhong
Liu, Chang
Du, Pingzhou
Li, Jingbin
Liu, Zengyu
Zhang, Fengli
Hou, Haili
Shi, Jianxin
Liang, Wanqi
Yang, Litao
Ren, Haiyun
Zhang, Dabing
OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis
title OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis
title_full OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis
title_fullStr OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis
title_full_unstemmed OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis
title_short OsFH3 Encodes a Type II Formin Required for Rice Morphogenesis
title_sort osfh3 encodes a type ii formin required for rice morphogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706662/
https://www.ncbi.nlm.nih.gov/pubmed/34948047
http://dx.doi.org/10.3390/ijms222413250
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