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The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants

The moss Physcomitrella patens is an ideal model plant to study plant developmental processes. To better understand the mechanism of protoplast regeneration, a phosphoproteome analysis was performed. Protoplasts were prepared from protonemata. By 4 d of protoplast regeneration, the first cell divisi...

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Autores principales: Wang, Xiaoqin, Qi, Meiyan, Li, Jingyun, Ji, Zhongzhong, Hu, Yong, Bao, Fang, Mahalingam, Ramamurthy, He, Yikun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991745/
https://www.ncbi.nlm.nih.gov/pubmed/24700621
http://dx.doi.org/10.1093/jxb/eru082
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author Wang, Xiaoqin
Qi, Meiyan
Li, Jingyun
Ji, Zhongzhong
Hu, Yong
Bao, Fang
Mahalingam, Ramamurthy
He, Yikun
author_facet Wang, Xiaoqin
Qi, Meiyan
Li, Jingyun
Ji, Zhongzhong
Hu, Yong
Bao, Fang
Mahalingam, Ramamurthy
He, Yikun
author_sort Wang, Xiaoqin
collection PubMed
description The moss Physcomitrella patens is an ideal model plant to study plant developmental processes. To better understand the mechanism of protoplast regeneration, a phosphoproteome analysis was performed. Protoplasts were prepared from protonemata. By 4 d of protoplast regeneration, the first cell divisions had ensued. Through a highly selective titanium dioxide (TiO(2))-based phosphopeptide enrichment method and mass spectrometric technology, more than 300 phosphoproteins were identified as protoplast regeneration responsive. Of these, 108 phosphoproteins were present on day 4 but not in fresh protoplasts or those cultured for 2 d. These proteins are catalogued here. They were involved in cell-wall metabolism, transcription, signal transduction, cell growth/division, and cell structure. These protein functions are related to cell morphogenesis, organogenesis, and development adjustment. This study presents a comprehensive analysis of phosphoproteome involved in protoplast regeneration and indicates that the mechanism of plant protoplast regeneration is similar to that of postembryonic development.
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spelling pubmed-39917452014-06-18 The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants Wang, Xiaoqin Qi, Meiyan Li, Jingyun Ji, Zhongzhong Hu, Yong Bao, Fang Mahalingam, Ramamurthy He, Yikun J Exp Bot Research Paper The moss Physcomitrella patens is an ideal model plant to study plant developmental processes. To better understand the mechanism of protoplast regeneration, a phosphoproteome analysis was performed. Protoplasts were prepared from protonemata. By 4 d of protoplast regeneration, the first cell divisions had ensued. Through a highly selective titanium dioxide (TiO(2))-based phosphopeptide enrichment method and mass spectrometric technology, more than 300 phosphoproteins were identified as protoplast regeneration responsive. Of these, 108 phosphoproteins were present on day 4 but not in fresh protoplasts or those cultured for 2 d. These proteins are catalogued here. They were involved in cell-wall metabolism, transcription, signal transduction, cell growth/division, and cell structure. These protein functions are related to cell morphogenesis, organogenesis, and development adjustment. This study presents a comprehensive analysis of phosphoproteome involved in protoplast regeneration and indicates that the mechanism of plant protoplast regeneration is similar to that of postembryonic development. Oxford University Press 2014-05 2014-04-03 /pmc/articles/PMC3991745/ /pubmed/24700621 http://dx.doi.org/10.1093/jxb/eru082 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Wang, Xiaoqin
Qi, Meiyan
Li, Jingyun
Ji, Zhongzhong
Hu, Yong
Bao, Fang
Mahalingam, Ramamurthy
He, Yikun
The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
title The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
title_full The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
title_fullStr The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
title_full_unstemmed The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
title_short The phosphoproteome in regenerating protoplasts from Physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
title_sort phosphoproteome in regenerating protoplasts from physcomitrella patens protonemata shows changes paralleling postembryonic development in higher plants
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991745/
https://www.ncbi.nlm.nih.gov/pubmed/24700621
http://dx.doi.org/10.1093/jxb/eru082
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