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The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane
Many filamentous plant pathogens place specialized feeding structures, called haustoria, inside living host cells. As haustoria grow, they are believed to manipulate plant cells to generate a specialized, still enigmatic extrahaustorial membrane (EHM) around them. Here, we focused on revealing prope...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854130/ https://www.ncbi.nlm.nih.gov/pubmed/29237056 http://dx.doi.org/10.1093/jxb/erx403 |
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author | Kwaaitaal, Mark Nielsen, Mads Eggert Böhlenius, Henrik Thordal-Christensen, Hans |
author_facet | Kwaaitaal, Mark Nielsen, Mads Eggert Böhlenius, Henrik Thordal-Christensen, Hans |
author_sort | Kwaaitaal, Mark |
collection | PubMed |
description | Many filamentous plant pathogens place specialized feeding structures, called haustoria, inside living host cells. As haustoria grow, they are believed to manipulate plant cells to generate a specialized, still enigmatic extrahaustorial membrane (EHM) around them. Here, we focused on revealing properties of the EHM. With the help of membrane-specific dyes and transient expression of membrane-associated proteins fused to fluorescent tags, we studied the nature of the EHM generated by barley leaf epidermal cells around powdery mildew haustoria. Observations suggesting that endoplasmic reticulum (ER) membrane-specific dyes labelled the EHM led us to find that Sar1 and RabD2a GTPases bind this membrane. These proteins are usually associated with the ER and the ER/cis-Golgi membrane, respectively. In contrast, transmembrane and luminal ER and Golgi markers failed to label the EHM, suggesting that it is not a continuum of the ER. Furthermore, GDP-locked Sar1 and a nucleotide-free RabD2a, which block ER to Golgi exit, did not hamper haustorium formation. These results indicated that the EHM shares features with the plant ER membrane, but that the EHM membrane is not dependent on conventional secretion. This raises the prospect that an unconventional secretory pathway from the ER may provide this membrane’s material. Understanding these processes will assist future approaches to providing resistance by preventing EHM generation. |
format | Online Article Text |
id | pubmed-5854130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58541302018-07-27 The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane Kwaaitaal, Mark Nielsen, Mads Eggert Böhlenius, Henrik Thordal-Christensen, Hans J Exp Bot Research Papers Many filamentous plant pathogens place specialized feeding structures, called haustoria, inside living host cells. As haustoria grow, they are believed to manipulate plant cells to generate a specialized, still enigmatic extrahaustorial membrane (EHM) around them. Here, we focused on revealing properties of the EHM. With the help of membrane-specific dyes and transient expression of membrane-associated proteins fused to fluorescent tags, we studied the nature of the EHM generated by barley leaf epidermal cells around powdery mildew haustoria. Observations suggesting that endoplasmic reticulum (ER) membrane-specific dyes labelled the EHM led us to find that Sar1 and RabD2a GTPases bind this membrane. These proteins are usually associated with the ER and the ER/cis-Golgi membrane, respectively. In contrast, transmembrane and luminal ER and Golgi markers failed to label the EHM, suggesting that it is not a continuum of the ER. Furthermore, GDP-locked Sar1 and a nucleotide-free RabD2a, which block ER to Golgi exit, did not hamper haustorium formation. These results indicated that the EHM shares features with the plant ER membrane, but that the EHM membrane is not dependent on conventional secretion. This raises the prospect that an unconventional secretory pathway from the ER may provide this membrane’s material. Understanding these processes will assist future approaches to providing resistance by preventing EHM generation. Oxford University Press 2017-12-16 2017-12-09 /pmc/articles/PMC5854130/ /pubmed/29237056 http://dx.doi.org/10.1093/jxb/erx403 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 Kwaaitaal, Mark Nielsen, Mads Eggert Böhlenius, Henrik Thordal-Christensen, Hans The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
title | The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
title_full | The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
title_fullStr | The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
title_full_unstemmed | The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
title_short | The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
title_sort | plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854130/ https://www.ncbi.nlm.nih.gov/pubmed/29237056 http://dx.doi.org/10.1093/jxb/erx403 |
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