Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
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
_version_ 1782357021840900096
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
work_keys_str_mv AT yangzhenzhen comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT wafulaerick comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT honaaslorena comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT zhanghuiting comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT dasmalay comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT fernandezapariciomonica comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT huangkan comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT bandaranayakepradeepacg comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT wubiao comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT derjoshuap comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT clarkechristopherr comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT ralphpaulae comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT landherrlena comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT altmannaomis comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT timkomichaelp comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT yoderjohni comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT westwoodjamesh comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty
AT depamphilisclaudew comparativetranscriptomeanalysesrevealcoreparasitismgenesandsuggestgeneduplicationandrepurposingassourcesofstructuralnovelty