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Host plant genetic control of associated fungal and insect species in a Populus hybrid cross
Plants employ a diverse set of defense mechanisms to mediate interactions with insects and fungi. These relationships can leave lasting impacts on host plant genome structure such as rapid expansion of gene families through tandem duplication. These genomic signatures provide important clues about t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297788/ https://www.ncbi.nlm.nih.gov/pubmed/32551087 http://dx.doi.org/10.1002/ece3.6266 |
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author | Simon, Sandra J. Tschaplinski, Timothy J. M. LeBoldus, Jared Keefover‐Ring, Ken Azeem, Muhammad Chen, Jin‐Gui Macaya‐Sanz, David MacDonald, William L. Muchero, Wellington DiFazio, Stephen P. |
author_facet | Simon, Sandra J. Tschaplinski, Timothy J. M. LeBoldus, Jared Keefover‐Ring, Ken Azeem, Muhammad Chen, Jin‐Gui Macaya‐Sanz, David MacDonald, William L. Muchero, Wellington DiFazio, Stephen P. |
author_sort | Simon, Sandra J. |
collection | PubMed |
description | Plants employ a diverse set of defense mechanisms to mediate interactions with insects and fungi. These relationships can leave lasting impacts on host plant genome structure such as rapid expansion of gene families through tandem duplication. These genomic signatures provide important clues about the complexities of plant/biotic stress interactions and evolution. We used a pseudo‐backcross hybrid family to identify quantitative trait loci (QTL) controlling associations between Populus trees and several common Populus diseases and insects. Using whole‐genome sequences from each parent, we identified candidate genes that may mediate these interactions. Candidates were partially validated using mass spectrometry to identify corresponding QTL for defensive compounds. We detected significant QTL for two interacting fungal pathogens and three insects. The QTL intervals contained candidate genes potentially involved in physical and chemical mechanisms of host–plant resistance and susceptibility. In particular, we identified adjoining QTLs for a phenolic glycoside and Phyllocolpa sawfly abundance. There was also significant enrichment of recent tandem duplications in the genomic intervals of the native parent, but not the exotic parent. Tandem gene duplication may be an important mechanism for rapid response to biotic stressors, enabling trees with long juvenile periods to reach maturity despite many coevolving biotic stressors. |
format | Online Article Text |
id | pubmed-7297788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72977882020-06-17 Host plant genetic control of associated fungal and insect species in a Populus hybrid cross Simon, Sandra J. Tschaplinski, Timothy J. M. LeBoldus, Jared Keefover‐Ring, Ken Azeem, Muhammad Chen, Jin‐Gui Macaya‐Sanz, David MacDonald, William L. Muchero, Wellington DiFazio, Stephen P. Ecol Evol Original Research Plants employ a diverse set of defense mechanisms to mediate interactions with insects and fungi. These relationships can leave lasting impacts on host plant genome structure such as rapid expansion of gene families through tandem duplication. These genomic signatures provide important clues about the complexities of plant/biotic stress interactions and evolution. We used a pseudo‐backcross hybrid family to identify quantitative trait loci (QTL) controlling associations between Populus trees and several common Populus diseases and insects. Using whole‐genome sequences from each parent, we identified candidate genes that may mediate these interactions. Candidates were partially validated using mass spectrometry to identify corresponding QTL for defensive compounds. We detected significant QTL for two interacting fungal pathogens and three insects. The QTL intervals contained candidate genes potentially involved in physical and chemical mechanisms of host–plant resistance and susceptibility. In particular, we identified adjoining QTLs for a phenolic glycoside and Phyllocolpa sawfly abundance. There was also significant enrichment of recent tandem duplications in the genomic intervals of the native parent, but not the exotic parent. Tandem gene duplication may be an important mechanism for rapid response to biotic stressors, enabling trees with long juvenile periods to reach maturity despite many coevolving biotic stressors. John Wiley and Sons Inc. 2020-04-27 /pmc/articles/PMC7297788/ /pubmed/32551087 http://dx.doi.org/10.1002/ece3.6266 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Simon, Sandra J. Tschaplinski, Timothy J. M. LeBoldus, Jared Keefover‐Ring, Ken Azeem, Muhammad Chen, Jin‐Gui Macaya‐Sanz, David MacDonald, William L. Muchero, Wellington DiFazio, Stephen P. Host plant genetic control of associated fungal and insect species in a Populus hybrid cross |
title | Host plant genetic control of associated fungal and insect species in a Populus hybrid cross |
title_full | Host plant genetic control of associated fungal and insect species in a Populus hybrid cross |
title_fullStr | Host plant genetic control of associated fungal and insect species in a Populus hybrid cross |
title_full_unstemmed | Host plant genetic control of associated fungal and insect species in a Populus hybrid cross |
title_short | Host plant genetic control of associated fungal and insect species in a Populus hybrid cross |
title_sort | host plant genetic control of associated fungal and insect species in a populus hybrid cross |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297788/ https://www.ncbi.nlm.nih.gov/pubmed/32551087 http://dx.doi.org/10.1002/ece3.6266 |
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