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Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty
The origin of novel traits is recognized as an important process underlying many major evolutionary radiations. We studied the genetic basis for the evolution of haustoria, the novel feeding organs of parasitic flowering plants, using comparative transcriptome sequencing in three species of Orobanch...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327159/ https://www.ncbi.nlm.nih.gov/pubmed/25534030 http://dx.doi.org/10.1093/molbev/msu343 |
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author | Yang, Zhenzhen Wafula, Eric K. Honaas, Loren A. Zhang, Huiting Das, Malay Fernandez-Aparicio, Monica Huang, Kan Bandaranayake, Pradeepa C.G. Wu, Biao Der, Joshua P. Clarke, Christopher R. Ralph, Paula E. Landherr, Lena Altman, Naomi S. Timko, Michael P. Yoder, John I. Westwood, James H. dePamphilis, Claude W. |
author_facet | Yang, Zhenzhen Wafula, Eric K. Honaas, Loren A. Zhang, Huiting Das, Malay Fernandez-Aparicio, Monica Huang, Kan Bandaranayake, Pradeepa C.G. Wu, Biao Der, Joshua P. Clarke, Christopher R. Ralph, Paula E. Landherr, Lena Altman, Naomi S. Timko, Michael P. Yoder, John I. Westwood, James H. dePamphilis, Claude W. |
author_sort | Yang, Zhenzhen |
collection | PubMed |
description | The origin of novel traits is recognized as an important process underlying many major evolutionary radiations. We studied the genetic basis for the evolution of haustoria, the novel feeding organs of parasitic flowering plants, using comparative transcriptome sequencing in three species of Orobanchaceae. Around 180 genes are upregulated during haustorial development following host attachment in at least two species, and these are enriched in proteases, cell wall modifying enzymes, and extracellular secretion proteins. Additionally, about 100 shared genes are upregulated in response to haustorium inducing factors prior to host attachment. Collectively, we refer to these newly identified genes as putative “parasitism genes.” Most of these parasitism genes are derived from gene duplications in a common ancestor of Orobanchaceae and Mimulus guttatus, a related nonparasitic plant. Additionally, the signature of relaxed purifying selection and/or adaptive evolution at specific sites was detected in many haustorial genes, and may play an important role in parasite evolution. Comparative analysis of gene expression patterns in parasitic and nonparasitic angiosperms suggests that parasitism genes are derived primarily from root and floral tissues, but with some genes co-opted from other tissues. Gene duplication, often taking place in a nonparasitic ancestor of Orobanchaceae, followed by regulatory neofunctionalization, was an important process in the origin of parasitic haustoria. |
format | Online Article Text |
id | pubmed-4327159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43271592015-02-26 Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty Yang, Zhenzhen Wafula, Eric K. Honaas, Loren A. Zhang, Huiting Das, Malay Fernandez-Aparicio, Monica Huang, Kan Bandaranayake, Pradeepa C.G. Wu, Biao Der, Joshua P. Clarke, Christopher R. Ralph, Paula E. Landherr, Lena Altman, Naomi S. Timko, Michael P. Yoder, John I. Westwood, James H. dePamphilis, Claude W. Mol Biol Evol Discoveries The origin of novel traits is recognized as an important process underlying many major evolutionary radiations. We studied the genetic basis for the evolution of haustoria, the novel feeding organs of parasitic flowering plants, using comparative transcriptome sequencing in three species of Orobanchaceae. Around 180 genes are upregulated during haustorial development following host attachment in at least two species, and these are enriched in proteases, cell wall modifying enzymes, and extracellular secretion proteins. Additionally, about 100 shared genes are upregulated in response to haustorium inducing factors prior to host attachment. Collectively, we refer to these newly identified genes as putative “parasitism genes.” Most of these parasitism genes are derived from gene duplications in a common ancestor of Orobanchaceae and Mimulus guttatus, a related nonparasitic plant. Additionally, the signature of relaxed purifying selection and/or adaptive evolution at specific sites was detected in many haustorial genes, and may play an important role in parasite evolution. Comparative analysis of gene expression patterns in parasitic and nonparasitic angiosperms suggests that parasitism genes are derived primarily from root and floral tissues, but with some genes co-opted from other tissues. Gene duplication, often taking place in a nonparasitic ancestor of Orobanchaceae, followed by regulatory neofunctionalization, was an important process in the origin of parasitic haustoria. Oxford University Press 2015-03 2014-12-21 /pmc/articles/PMC4327159/ /pubmed/25534030 http://dx.doi.org/10.1093/molbev/msu343 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Yang, Zhenzhen Wafula, Eric K. Honaas, Loren A. Zhang, Huiting Das, Malay Fernandez-Aparicio, Monica Huang, Kan Bandaranayake, Pradeepa C.G. Wu, Biao Der, Joshua P. Clarke, Christopher R. Ralph, Paula E. Landherr, Lena Altman, Naomi S. Timko, Michael P. Yoder, John I. Westwood, James H. dePamphilis, Claude W. Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty |
title | Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty |
title_full | Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty |
title_fullStr | Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty |
title_full_unstemmed | Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty |
title_short | Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty |
title_sort | comparative transcriptome analyses reveal core parasitism genes and suggest gene duplication and repurposing as sources of structural novelty |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327159/ https://www.ncbi.nlm.nih.gov/pubmed/25534030 http://dx.doi.org/10.1093/molbev/msu343 |
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