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Comparative phyloproteomics identifies conserved plasmodesmal proteins
Plasmodesmata are cytosolic bridges, lined by the plasma membrane and traversed by endoplasmic reticulum; plasmodesmata connect cells and tissues, and are critical for many aspects of plant biology. While plasmodesmata are notoriously difficult to extract, tissue fractionation and proteomic analyses...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049917/ https://www.ncbi.nlm.nih.gov/pubmed/36639877 http://dx.doi.org/10.1093/jxb/erad022 |
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author | Johnston, Matthew G Breakspear, Andrew Samwald, Sebastian Zhang, Dan Papp, Diana Faulkner, Christine de Keijzer, Jeroen |
author_facet | Johnston, Matthew G Breakspear, Andrew Samwald, Sebastian Zhang, Dan Papp, Diana Faulkner, Christine de Keijzer, Jeroen |
author_sort | Johnston, Matthew G |
collection | PubMed |
description | Plasmodesmata are cytosolic bridges, lined by the plasma membrane and traversed by endoplasmic reticulum; plasmodesmata connect cells and tissues, and are critical for many aspects of plant biology. While plasmodesmata are notoriously difficult to extract, tissue fractionation and proteomic analyses can yield valuable knowledge of their composition. Here we have generated two novel proteomes to expand tissue and taxonomic representation of plasmodesmata: one from mature Arabidopsis leaves and one from the moss Physcomitrium patens, and leveraged these and existing data to perform a comparative analysis to identify evolutionarily conserved protein families that are associated with plasmodesmata. Thus, we identified β-1,3-glucanases, C2 lipid-binding proteins, and tetraspanins as core plasmodesmal components that probably serve as essential structural or functional components. Our approach has not only identified elements of a conserved plasmodesmal proteome, but also demonstrated the added power offered by comparative analysis for recalcitrant samples. Conserved plasmodesmal proteins establish a basis upon which ancient plasmodesmal function can be further investigated to determine the essential roles these structures play in multicellular organism physiology in the green lineages. |
format | Online Article Text |
id | pubmed-10049917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100499172023-03-30 Comparative phyloproteomics identifies conserved plasmodesmal proteins Johnston, Matthew G Breakspear, Andrew Samwald, Sebastian Zhang, Dan Papp, Diana Faulkner, Christine de Keijzer, Jeroen J Exp Bot Research Papers Plasmodesmata are cytosolic bridges, lined by the plasma membrane and traversed by endoplasmic reticulum; plasmodesmata connect cells and tissues, and are critical for many aspects of plant biology. While plasmodesmata are notoriously difficult to extract, tissue fractionation and proteomic analyses can yield valuable knowledge of their composition. Here we have generated two novel proteomes to expand tissue and taxonomic representation of plasmodesmata: one from mature Arabidopsis leaves and one from the moss Physcomitrium patens, and leveraged these and existing data to perform a comparative analysis to identify evolutionarily conserved protein families that are associated with plasmodesmata. Thus, we identified β-1,3-glucanases, C2 lipid-binding proteins, and tetraspanins as core plasmodesmal components that probably serve as essential structural or functional components. Our approach has not only identified elements of a conserved plasmodesmal proteome, but also demonstrated the added power offered by comparative analysis for recalcitrant samples. Conserved plasmodesmal proteins establish a basis upon which ancient plasmodesmal function can be further investigated to determine the essential roles these structures play in multicellular organism physiology in the green lineages. Oxford University Press 2023-01-14 /pmc/articles/PMC10049917/ /pubmed/36639877 http://dx.doi.org/10.1093/jxb/erad022 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Johnston, Matthew G Breakspear, Andrew Samwald, Sebastian Zhang, Dan Papp, Diana Faulkner, Christine de Keijzer, Jeroen Comparative phyloproteomics identifies conserved plasmodesmal proteins |
title | Comparative phyloproteomics identifies conserved plasmodesmal proteins |
title_full | Comparative phyloproteomics identifies conserved plasmodesmal proteins |
title_fullStr | Comparative phyloproteomics identifies conserved plasmodesmal proteins |
title_full_unstemmed | Comparative phyloproteomics identifies conserved plasmodesmal proteins |
title_short | Comparative phyloproteomics identifies conserved plasmodesmal proteins |
title_sort | comparative phyloproteomics identifies conserved plasmodesmal proteins |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049917/ https://www.ncbi.nlm.nih.gov/pubmed/36639877 http://dx.doi.org/10.1093/jxb/erad022 |
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