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Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds

Seed germination is a complicated biological process that requires regulated enzymatic and non-enzymatic reactions. The action of polyamine oxidase (PAO) produces hydrogen peroxide (H(2)O(2)), which promotes dicot seed germination. However, whether and, if so, how PAOs regulate monocot seed germinat...

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Autores principales: Chen, Bing-Xian, Li, Wen-Yan, Gao, Yin-Tao, Chen, Zhong-Jian, Zhang, Wei-Na, Liu, Qin-Jian, Chen, Zhuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981591/
https://www.ncbi.nlm.nih.gov/pubmed/27570530
http://dx.doi.org/10.3389/fpls.2016.01219
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author Chen, Bing-Xian
Li, Wen-Yan
Gao, Yin-Tao
Chen, Zhong-Jian
Zhang, Wei-Na
Liu, Qin-Jian
Chen, Zhuang
author_facet Chen, Bing-Xian
Li, Wen-Yan
Gao, Yin-Tao
Chen, Zhong-Jian
Zhang, Wei-Na
Liu, Qin-Jian
Chen, Zhuang
author_sort Chen, Bing-Xian
collection PubMed
description Seed germination is a complicated biological process that requires regulated enzymatic and non-enzymatic reactions. The action of polyamine oxidase (PAO) produces hydrogen peroxide (H(2)O(2)), which promotes dicot seed germination. However, whether and, if so, how PAOs regulate monocot seed germination via H(2)O(2) production is unclear. Herein, we report that the coleorhiza is the main physical barrier to radicle protrusion during germination of rice seed (a monocot seed) and that it does so in a manner similar to that of dicot seed micropylar endosperm. We found that H(2)O(2) specifically and steadily accumulated in the coleorhizae and radicles of germinating rice seeds and was accompanied by increased PAO activity as the germination percentage increased. These physiological indexes were strongly decreased in number by guazatine, a PAO inhibitor. We also identified 11 PAO homologs (OsPAO1–11) in the rice genome, which could be classified into four subfamilies (I, IIa, IIb, and III). The OsPAO genes in subfamilies I, IIa, and IIb (OsPAO1–7) encode PAOs, whereas those in subfamily III (OsPAO8–11) encode histone lysine-specific demethylases. In silico-characterized expression profiles of OsPAO1–7 and those determined by qPCR revealed that OsPAO5 is markedly upregulated in imbibed seeds compared with dry seeds and that its transcript accumulated to a higher level in embryos than in the endosperm. Moreover, its transcriptional abundance increased gradually during seed germination in water and was inhibited by 5 mM guazatine. Taken together, these results suggest that PAO-generated H(2)O(2) is involved in coleorhiza-limited rice seed germination and that OsPAO5 expression accounts for most PAO expression and activity during rice seed germination. These findings should facilitate further study of PAOs and provide valuable information for functional validation of these proteins during seed germination of monocot cereals.
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spelling pubmed-49815912016-08-26 Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds Chen, Bing-Xian Li, Wen-Yan Gao, Yin-Tao Chen, Zhong-Jian Zhang, Wei-Na Liu, Qin-Jian Chen, Zhuang Front Plant Sci Plant Science Seed germination is a complicated biological process that requires regulated enzymatic and non-enzymatic reactions. The action of polyamine oxidase (PAO) produces hydrogen peroxide (H(2)O(2)), which promotes dicot seed germination. However, whether and, if so, how PAOs regulate monocot seed germination via H(2)O(2) production is unclear. Herein, we report that the coleorhiza is the main physical barrier to radicle protrusion during germination of rice seed (a monocot seed) and that it does so in a manner similar to that of dicot seed micropylar endosperm. We found that H(2)O(2) specifically and steadily accumulated in the coleorhizae and radicles of germinating rice seeds and was accompanied by increased PAO activity as the germination percentage increased. These physiological indexes were strongly decreased in number by guazatine, a PAO inhibitor. We also identified 11 PAO homologs (OsPAO1–11) in the rice genome, which could be classified into four subfamilies (I, IIa, IIb, and III). The OsPAO genes in subfamilies I, IIa, and IIb (OsPAO1–7) encode PAOs, whereas those in subfamily III (OsPAO8–11) encode histone lysine-specific demethylases. In silico-characterized expression profiles of OsPAO1–7 and those determined by qPCR revealed that OsPAO5 is markedly upregulated in imbibed seeds compared with dry seeds and that its transcript accumulated to a higher level in embryos than in the endosperm. Moreover, its transcriptional abundance increased gradually during seed germination in water and was inhibited by 5 mM guazatine. Taken together, these results suggest that PAO-generated H(2)O(2) is involved in coleorhiza-limited rice seed germination and that OsPAO5 expression accounts for most PAO expression and activity during rice seed germination. These findings should facilitate further study of PAOs and provide valuable information for functional validation of these proteins during seed germination of monocot cereals. Frontiers Media S.A. 2016-08-12 /pmc/articles/PMC4981591/ /pubmed/27570530 http://dx.doi.org/10.3389/fpls.2016.01219 Text en Copyright © 2016 Chen, Li, Gao, Chen, Zhang, Liu and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Chen, Bing-Xian
Li, Wen-Yan
Gao, Yin-Tao
Chen, Zhong-Jian
Zhang, Wei-Na
Liu, Qin-Jian
Chen, Zhuang
Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds
title Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds
title_full Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds
title_fullStr Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds
title_full_unstemmed Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds
title_short Involvement of Polyamine Oxidase-Produced Hydrogen Peroxide during Coleorhiza-Limited Germination of Rice Seeds
title_sort involvement of polyamine oxidase-produced hydrogen peroxide during coleorhiza-limited germination of rice seeds
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981591/
https://www.ncbi.nlm.nih.gov/pubmed/27570530
http://dx.doi.org/10.3389/fpls.2016.01219
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