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Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons
Parasites are able to evolve rapidly and overcome host defense mechanisms, but the molecular basis of this adaptation is poorly understood. Powdery mildew fungi (Erysiphales, Ascomycota) are obligate biotrophic parasites infecting nearly 10,000 plant genera. They obtain their nutrients from host pla...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759079/ https://www.ncbi.nlm.nih.gov/pubmed/19829700 http://dx.doi.org/10.1371/journal.pone.0007463 |
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author | Sacristán, Soledad Vigouroux, Marielle Pedersen, Carsten Skamnioti, Pari Thordal-Christensen, Hans Micali, Cristina Brown, James K. M. Ridout, Christopher J. |
author_facet | Sacristán, Soledad Vigouroux, Marielle Pedersen, Carsten Skamnioti, Pari Thordal-Christensen, Hans Micali, Cristina Brown, James K. M. Ridout, Christopher J. |
author_sort | Sacristán, Soledad |
collection | PubMed |
description | Parasites are able to evolve rapidly and overcome host defense mechanisms, but the molecular basis of this adaptation is poorly understood. Powdery mildew fungi (Erysiphales, Ascomycota) are obligate biotrophic parasites infecting nearly 10,000 plant genera. They obtain their nutrients from host plants through specialized feeding structures known as haustoria. We previously identified the AVR (k1) powdery mildew-specific gene family encoding effectors that contribute to the successful establishment of haustoria. Here, we report the extensive proliferation of the AVR (k1) gene family throughout the genome of B. graminis, with sequences diverging in formae speciales adapted to infect different hosts. Also, importantly, we have discovered that the effectors have coevolved with a particular family of LINE-1 retrotransposons, named TE1a. The coevolution of these two entities indicates a mutual benefit to the association, which could ultimately contribute to parasite adaptation and success. We propose that the association would benefit 1) the powdery mildew fungus, by providing a mechanism for amplifying and diversifying effectors and 2) the associated retrotransposons, by providing a basis for their maintenance through selection in the fungal genome. |
format | Text |
id | pubmed-2759079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27590792009-10-15 Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons Sacristán, Soledad Vigouroux, Marielle Pedersen, Carsten Skamnioti, Pari Thordal-Christensen, Hans Micali, Cristina Brown, James K. M. Ridout, Christopher J. PLoS One Research Article Parasites are able to evolve rapidly and overcome host defense mechanisms, but the molecular basis of this adaptation is poorly understood. Powdery mildew fungi (Erysiphales, Ascomycota) are obligate biotrophic parasites infecting nearly 10,000 plant genera. They obtain their nutrients from host plants through specialized feeding structures known as haustoria. We previously identified the AVR (k1) powdery mildew-specific gene family encoding effectors that contribute to the successful establishment of haustoria. Here, we report the extensive proliferation of the AVR (k1) gene family throughout the genome of B. graminis, with sequences diverging in formae speciales adapted to infect different hosts. Also, importantly, we have discovered that the effectors have coevolved with a particular family of LINE-1 retrotransposons, named TE1a. The coevolution of these two entities indicates a mutual benefit to the association, which could ultimately contribute to parasite adaptation and success. We propose that the association would benefit 1) the powdery mildew fungus, by providing a mechanism for amplifying and diversifying effectors and 2) the associated retrotransposons, by providing a basis for their maintenance through selection in the fungal genome. Public Library of Science 2009-10-15 /pmc/articles/PMC2759079/ /pubmed/19829700 http://dx.doi.org/10.1371/journal.pone.0007463 Text en Sacristán et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sacristán, Soledad Vigouroux, Marielle Pedersen, Carsten Skamnioti, Pari Thordal-Christensen, Hans Micali, Cristina Brown, James K. M. Ridout, Christopher J. Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons |
title | Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons |
title_full | Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons |
title_fullStr | Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons |
title_full_unstemmed | Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons |
title_short | Coevolution between a Family of Parasite Virulence Effectors and a Class of LINE-1 Retrotransposons |
title_sort | coevolution between a family of parasite virulence effectors and a class of line-1 retrotransposons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759079/ https://www.ncbi.nlm.nih.gov/pubmed/19829700 http://dx.doi.org/10.1371/journal.pone.0007463 |
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