Cargando…
Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression
BACKGROUND: Orobanchaceae is the only plant family with members representing the full range of parasitic lifestyles plus a free-living lineage sister to all parasitic lineages, Lindenbergia. A generalist member of this family, and an important parasitic plant model, Triphysaria versicolor regularly...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636017/ https://www.ncbi.nlm.nih.gov/pubmed/23302495 http://dx.doi.org/10.1186/1471-2229-13-9 |
_version_ | 1782267256884953088 |
---|---|
author | Honaas, Loren A Wafula, Eric K Yang, Zhenzhen Der, Joshua P Wickett, Norman J Altman, Naomi S Taylor, Christopher G Yoder, John I Timko, Michael P Westwood, James H dePamphilis, Claude W |
author_facet | Honaas, Loren A Wafula, Eric K Yang, Zhenzhen Der, Joshua P Wickett, Norman J Altman, Naomi S Taylor, Christopher G Yoder, John I Timko, Michael P Westwood, James H dePamphilis, Claude W |
author_sort | Honaas, Loren A |
collection | PubMed |
description | BACKGROUND: Orobanchaceae is the only plant family with members representing the full range of parasitic lifestyles plus a free-living lineage sister to all parasitic lineages, Lindenbergia. A generalist member of this family, and an important parasitic plant model, Triphysaria versicolor regularly feeds upon a wide range of host plants. Here, we compare de novo assembled transcriptomes generated from laser micro-dissected tissues at the host-parasite interface to uncover details of the largely uncharacterized interaction between parasitic plants and their hosts. RESULTS: The interaction of Triphysaria with the distantly related hosts Zea mays and Medicago truncatula reveals dramatic host-specific gene expression patterns. Relative to above ground tissues, gene families are disproportionally represented at the interface including enrichment for transcription factors and genes of unknown function. Quantitative Real-Time PCR of a T. versicolor β-expansin shows strong differential (120x) upregulation in response to the monocot host Z. mays; a result that is concordant with our read count estimates. Pathogenesis-related proteins, other cell wall modifying enzymes, and orthologs of genes with unknown function (annotated as such in sequenced plant genomes) are among the parasite genes highly expressed by T. versicolor at the parasite-host interface. CONCLUSIONS: Laser capture microdissection makes it possible to sample the small region of cells at the epicenter of parasite host interactions. The results of our analysis suggest that T. versicolor’s generalist strategy involves a reliance on overlapping but distinct gene sets, depending upon the host plant it is parasitizing. The massive upregulation of a T. versicolor β-expansin is suggestive of a mechanism for parasite success on grass hosts. In this preliminary study of the interface transcriptomes, we have shown that T. versicolor, and the Orobanchaceae in general, provide excellent opportunities for the characterization of plant genes with unknown functions. |
format | Online Article Text |
id | pubmed-3636017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36360172013-04-26 Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression Honaas, Loren A Wafula, Eric K Yang, Zhenzhen Der, Joshua P Wickett, Norman J Altman, Naomi S Taylor, Christopher G Yoder, John I Timko, Michael P Westwood, James H dePamphilis, Claude W BMC Plant Biol Research Article BACKGROUND: Orobanchaceae is the only plant family with members representing the full range of parasitic lifestyles plus a free-living lineage sister to all parasitic lineages, Lindenbergia. A generalist member of this family, and an important parasitic plant model, Triphysaria versicolor regularly feeds upon a wide range of host plants. Here, we compare de novo assembled transcriptomes generated from laser micro-dissected tissues at the host-parasite interface to uncover details of the largely uncharacterized interaction between parasitic plants and their hosts. RESULTS: The interaction of Triphysaria with the distantly related hosts Zea mays and Medicago truncatula reveals dramatic host-specific gene expression patterns. Relative to above ground tissues, gene families are disproportionally represented at the interface including enrichment for transcription factors and genes of unknown function. Quantitative Real-Time PCR of a T. versicolor β-expansin shows strong differential (120x) upregulation in response to the monocot host Z. mays; a result that is concordant with our read count estimates. Pathogenesis-related proteins, other cell wall modifying enzymes, and orthologs of genes with unknown function (annotated as such in sequenced plant genomes) are among the parasite genes highly expressed by T. versicolor at the parasite-host interface. CONCLUSIONS: Laser capture microdissection makes it possible to sample the small region of cells at the epicenter of parasite host interactions. The results of our analysis suggest that T. versicolor’s generalist strategy involves a reliance on overlapping but distinct gene sets, depending upon the host plant it is parasitizing. The massive upregulation of a T. versicolor β-expansin is suggestive of a mechanism for parasite success on grass hosts. In this preliminary study of the interface transcriptomes, we have shown that T. versicolor, and the Orobanchaceae in general, provide excellent opportunities for the characterization of plant genes with unknown functions. BioMed Central 2013-01-09 /pmc/articles/PMC3636017/ /pubmed/23302495 http://dx.doi.org/10.1186/1471-2229-13-9 Text en Copyright © 2013 Honaas et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Honaas, Loren A Wafula, Eric K Yang, Zhenzhen Der, Joshua P Wickett, Norman J Altman, Naomi S Taylor, Christopher G Yoder, John I Timko, Michael P Westwood, James H dePamphilis, Claude W Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
title | Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
title_full | Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
title_fullStr | Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
title_full_unstemmed | Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
title_short | Functional genomics of a generalist parasitic plant: Laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
title_sort | functional genomics of a generalist parasitic plant: laser microdissection of host-parasite interface reveals host-specific patterns of parasite gene expression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636017/ https://www.ncbi.nlm.nih.gov/pubmed/23302495 http://dx.doi.org/10.1186/1471-2229-13-9 |
work_keys_str_mv | AT honaaslorena functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT wafulaerick functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT yangzhenzhen functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT derjoshuap functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT wickettnormanj functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT altmannaomis functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT taylorchristopherg functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT yoderjohni functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT timkomichaelp functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT westwoodjamesh functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression AT depamphilisclaudew functionalgenomicsofageneralistparasiticplantlasermicrodissectionofhostparasiteinterfacerevealshostspecificpatternsofparasitegeneexpression |