Cargando…

Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree

Invasive microbes causing diseases such as sudden oak death negatively affect ecosystems and economies around the world. The deployment of resistant genotypes for combating introduced diseases typically relies on breeding programs that can take decades to complete. To demonstrate how this process ca...

Descripción completa

Detalles Bibliográficos
Autores principales: Muchero, Wellington, Sondreli, Kelsey L., Chen, Jin-Gui, Urbanowicz, Breeanna R., Zhang, Jin, Singan, Vasanth, Yang, Yongil, Brueggeman, Robert S., Franco-Coronado, Juan, Abraham, Nivi, Yang, Jeong-Yeh, Moremen, Kelley W., Weisberg, Alexandra J., Chang, Jeff H., Lindquist, Erika, Barry, Kerrie, Ranjan, Priya, Jawdy, Sara, Schmutz, Jeremy, Tuskan, Gerald A., LeBoldus, Jared M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233113/
https://www.ncbi.nlm.nih.gov/pubmed/30337484
http://dx.doi.org/10.1073/pnas.1804428115
_version_ 1783370522239696896
author Muchero, Wellington
Sondreli, Kelsey L.
Chen, Jin-Gui
Urbanowicz, Breeanna R.
Zhang, Jin
Singan, Vasanth
Yang, Yongil
Brueggeman, Robert S.
Franco-Coronado, Juan
Abraham, Nivi
Yang, Jeong-Yeh
Moremen, Kelley W.
Weisberg, Alexandra J.
Chang, Jeff H.
Lindquist, Erika
Barry, Kerrie
Ranjan, Priya
Jawdy, Sara
Schmutz, Jeremy
Tuskan, Gerald A.
LeBoldus, Jared M.
author_facet Muchero, Wellington
Sondreli, Kelsey L.
Chen, Jin-Gui
Urbanowicz, Breeanna R.
Zhang, Jin
Singan, Vasanth
Yang, Yongil
Brueggeman, Robert S.
Franco-Coronado, Juan
Abraham, Nivi
Yang, Jeong-Yeh
Moremen, Kelley W.
Weisberg, Alexandra J.
Chang, Jeff H.
Lindquist, Erika
Barry, Kerrie
Ranjan, Priya
Jawdy, Sara
Schmutz, Jeremy
Tuskan, Gerald A.
LeBoldus, Jared M.
author_sort Muchero, Wellington
collection PubMed
description Invasive microbes causing diseases such as sudden oak death negatively affect ecosystems and economies around the world. The deployment of resistant genotypes for combating introduced diseases typically relies on breeding programs that can take decades to complete. To demonstrate how this process can be accelerated, we employed a genome-wide association mapping of ca. 1,000 resequenced Populus trichocarpa trees individually challenged with Sphaerulina musiva, an invasive fungal pathogen. Among significant associations, three loci associated with resistance were identified and predicted to encode one putative membrane-bound L-type receptor-like kinase and two receptor-like proteins. A susceptibility-associated locus was predicted to encode a putative G-type D-mannose–binding receptor-like kinase. Multiple lines of evidence, including allele analysis, transcriptomics, binding assays, and overexpression, support the hypothesized function of these candidate genes in the P. trichocarpa response to S. musiva.
format Online
Article
Text
id pubmed-6233113
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-62331132018-11-14 Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree Muchero, Wellington Sondreli, Kelsey L. Chen, Jin-Gui Urbanowicz, Breeanna R. Zhang, Jin Singan, Vasanth Yang, Yongil Brueggeman, Robert S. Franco-Coronado, Juan Abraham, Nivi Yang, Jeong-Yeh Moremen, Kelley W. Weisberg, Alexandra J. Chang, Jeff H. Lindquist, Erika Barry, Kerrie Ranjan, Priya Jawdy, Sara Schmutz, Jeremy Tuskan, Gerald A. LeBoldus, Jared M. Proc Natl Acad Sci U S A Biological Sciences Invasive microbes causing diseases such as sudden oak death negatively affect ecosystems and economies around the world. The deployment of resistant genotypes for combating introduced diseases typically relies on breeding programs that can take decades to complete. To demonstrate how this process can be accelerated, we employed a genome-wide association mapping of ca. 1,000 resequenced Populus trichocarpa trees individually challenged with Sphaerulina musiva, an invasive fungal pathogen. Among significant associations, three loci associated with resistance were identified and predicted to encode one putative membrane-bound L-type receptor-like kinase and two receptor-like proteins. A susceptibility-associated locus was predicted to encode a putative G-type D-mannose–binding receptor-like kinase. Multiple lines of evidence, including allele analysis, transcriptomics, binding assays, and overexpression, support the hypothesized function of these candidate genes in the P. trichocarpa response to S. musiva. National Academy of Sciences 2018-11-06 2018-10-18 /pmc/articles/PMC6233113/ /pubmed/30337484 http://dx.doi.org/10.1073/pnas.1804428115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Muchero, Wellington
Sondreli, Kelsey L.
Chen, Jin-Gui
Urbanowicz, Breeanna R.
Zhang, Jin
Singan, Vasanth
Yang, Yongil
Brueggeman, Robert S.
Franco-Coronado, Juan
Abraham, Nivi
Yang, Jeong-Yeh
Moremen, Kelley W.
Weisberg, Alexandra J.
Chang, Jeff H.
Lindquist, Erika
Barry, Kerrie
Ranjan, Priya
Jawdy, Sara
Schmutz, Jeremy
Tuskan, Gerald A.
LeBoldus, Jared M.
Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
title Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
title_full Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
title_fullStr Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
title_full_unstemmed Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
title_short Association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
title_sort association mapping, transcriptomics, and transient expression identify candidate genes mediating plant–pathogen interactions in a tree
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233113/
https://www.ncbi.nlm.nih.gov/pubmed/30337484
http://dx.doi.org/10.1073/pnas.1804428115
work_keys_str_mv AT mucherowellington associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT sondrelikelseyl associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT chenjingui associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT urbanowiczbreeannar associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT zhangjin associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT singanvasanth associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT yangyongil associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT brueggemanroberts associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT francocoronadojuan associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT abrahamnivi associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT yangjeongyeh associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT moremenkelleyw associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT weisbergalexandraj associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT changjeffh associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT lindquisterika associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT barrykerrie associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT ranjanpriya associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT jawdysara associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT schmutzjeremy associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT tuskangeralda associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree
AT leboldusjaredm associationmappingtranscriptomicsandtransientexpressionidentifycandidategenesmediatingplantpathogeninteractionsinatree