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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-3991745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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