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Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis
Our understanding of the contribution of Golgi proteins to cell wall and wood formation in any woody plant species is limited. Currently, little Golgi proteomics data exists for wood-forming tissues. In this study, we attempted to address this issue by generating and analyzing Golgi-enriched membran...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887118/ https://www.ncbi.nlm.nih.gov/pubmed/24416096 http://dx.doi.org/10.1371/journal.pone.0084669 |
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author | Parsons, Harriet T. Weinberg, Cristina S. Macdonald, Lucy J. Adams, Paul D. Petzold, Christopher J. Strabala, Timothy J. Wagner, Armin Heazlewood, Joshua L. |
author_facet | Parsons, Harriet T. Weinberg, Cristina S. Macdonald, Lucy J. Adams, Paul D. Petzold, Christopher J. Strabala, Timothy J. Wagner, Armin Heazlewood, Joshua L. |
author_sort | Parsons, Harriet T. |
collection | PubMed |
description | Our understanding of the contribution of Golgi proteins to cell wall and wood formation in any woody plant species is limited. Currently, little Golgi proteomics data exists for wood-forming tissues. In this study, we attempted to address this issue by generating and analyzing Golgi-enriched membrane preparations from developing xylem of compression wood from the conifer Pinus radiata. Developing xylem samples from 3-year-old pine trees were harvested for this purpose at a time of active growth and subjected to a combination of density centrifugation followed by free flow electrophoresis, a surface charge separation technique used in the enrichment of Golgi membranes. This combination of techniques was successful in achieving an approximately 200-fold increase in the activity of the Golgi marker galactan synthase and represents a significant improvement for proteomic analyses of the Golgi from conifers. A total of thirty known Golgi proteins were identified by mass spectrometry including glycosyltransferases from gene families involved in glucomannan and glucuronoxylan biosynthesis. The free flow electrophoresis fractions of enriched Golgi were highly abundant in structural proteins (actin and tubulin) indicating a role for the cytoskeleton during compression wood formation. The mass spectrometry proteomics data associated with this study have been deposited to the ProteomeXchange with identifier PXD000557. |
format | Online Article Text |
id | pubmed-3887118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38871182014-01-10 Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis Parsons, Harriet T. Weinberg, Cristina S. Macdonald, Lucy J. Adams, Paul D. Petzold, Christopher J. Strabala, Timothy J. Wagner, Armin Heazlewood, Joshua L. PLoS One Research Article Our understanding of the contribution of Golgi proteins to cell wall and wood formation in any woody plant species is limited. Currently, little Golgi proteomics data exists for wood-forming tissues. In this study, we attempted to address this issue by generating and analyzing Golgi-enriched membrane preparations from developing xylem of compression wood from the conifer Pinus radiata. Developing xylem samples from 3-year-old pine trees were harvested for this purpose at a time of active growth and subjected to a combination of density centrifugation followed by free flow electrophoresis, a surface charge separation technique used in the enrichment of Golgi membranes. This combination of techniques was successful in achieving an approximately 200-fold increase in the activity of the Golgi marker galactan synthase and represents a significant improvement for proteomic analyses of the Golgi from conifers. A total of thirty known Golgi proteins were identified by mass spectrometry including glycosyltransferases from gene families involved in glucomannan and glucuronoxylan biosynthesis. The free flow electrophoresis fractions of enriched Golgi were highly abundant in structural proteins (actin and tubulin) indicating a role for the cytoskeleton during compression wood formation. The mass spectrometry proteomics data associated with this study have been deposited to the ProteomeXchange with identifier PXD000557. Public Library of Science 2013-12-26 /pmc/articles/PMC3887118/ /pubmed/24416096 http://dx.doi.org/10.1371/journal.pone.0084669 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Parsons, Harriet T. Weinberg, Cristina S. Macdonald, Lucy J. Adams, Paul D. Petzold, Christopher J. Strabala, Timothy J. Wagner, Armin Heazlewood, Joshua L. Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis |
title | Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis |
title_full | Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis |
title_fullStr | Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis |
title_full_unstemmed | Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis |
title_short | Golgi Enrichment and Proteomic Analysis of Developing Pinus radiata Xylem by Free-Flow Electrophoresis |
title_sort | golgi enrichment and proteomic analysis of developing pinus radiata xylem by free-flow electrophoresis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887118/ https://www.ncbi.nlm.nih.gov/pubmed/24416096 http://dx.doi.org/10.1371/journal.pone.0084669 |
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