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The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility

Plant pathogens cause significant crop loss worldwide, and new resistance genes deployed to combat diseases can be overcome quickly. Understanding the existing resistance gene diversity within the germplasm of major crops, such as maize, is crucial for the development of new disease‐resistant variet...

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Autores principales: Thatcher, Shawn, Jung, Mark, Panangipalli, Gayathri, Fengler, Kevin, Sanyal, Abhijit, Li, Bailin, Llaca, Victor, Habben, Jeffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257044/
https://www.ncbi.nlm.nih.gov/pubmed/36929631
http://dx.doi.org/10.1111/mpp.13319
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author Thatcher, Shawn
Jung, Mark
Panangipalli, Gayathri
Fengler, Kevin
Sanyal, Abhijit
Li, Bailin
Llaca, Victor
Habben, Jeffrey
author_facet Thatcher, Shawn
Jung, Mark
Panangipalli, Gayathri
Fengler, Kevin
Sanyal, Abhijit
Li, Bailin
Llaca, Victor
Habben, Jeffrey
author_sort Thatcher, Shawn
collection PubMed
description Plant pathogens cause significant crop loss worldwide, and new resistance genes deployed to combat diseases can be overcome quickly. Understanding the existing resistance gene diversity within the germplasm of major crops, such as maize, is crucial for the development of new disease‐resistant varieties. We analysed the nucleotide‐binding leucine‐rich repeat receptors (NLRs) of 26 recently sequenced diverse founder lines from the maize nested association mapping (NAM) population and compared them to the R gene complement present in a wild relative of maize, Zea luxurians. We found that NLRs in both species contain a large diversity of atypical integrated domains, including many domains that have not previously been found in the NLRs of other species. Additionally, the single Z. luxurians genome was found to have greater integrated atypical domain diversity than all 26 NAM founder lines combined, indicating that this species may represent a rich source of novel resistance genes. NLRs were also found to have very high sequence diversity and presence–absence variation among the NAM founder lines, with a large NLR cluster on Chr10 representing a diversity hotspot. Additionally, NLRs were shown to be mobile within maize genomes, with several putative interchromosomal translocations identified.
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spelling pubmed-102570442023-06-11 The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility Thatcher, Shawn Jung, Mark Panangipalli, Gayathri Fengler, Kevin Sanyal, Abhijit Li, Bailin Llaca, Victor Habben, Jeffrey Mol Plant Pathol Original Articles Plant pathogens cause significant crop loss worldwide, and new resistance genes deployed to combat diseases can be overcome quickly. Understanding the existing resistance gene diversity within the germplasm of major crops, such as maize, is crucial for the development of new disease‐resistant varieties. We analysed the nucleotide‐binding leucine‐rich repeat receptors (NLRs) of 26 recently sequenced diverse founder lines from the maize nested association mapping (NAM) population and compared them to the R gene complement present in a wild relative of maize, Zea luxurians. We found that NLRs in both species contain a large diversity of atypical integrated domains, including many domains that have not previously been found in the NLRs of other species. Additionally, the single Z. luxurians genome was found to have greater integrated atypical domain diversity than all 26 NAM founder lines combined, indicating that this species may represent a rich source of novel resistance genes. NLRs were also found to have very high sequence diversity and presence–absence variation among the NAM founder lines, with a large NLR cluster on Chr10 representing a diversity hotspot. Additionally, NLRs were shown to be mobile within maize genomes, with several putative interchromosomal translocations identified. John Wiley and Sons Inc. 2023-03-16 /pmc/articles/PMC10257044/ /pubmed/36929631 http://dx.doi.org/10.1111/mpp.13319 Text en © 2023 Corteva Agriscience. Molecular Plant Pathology published by John Wiley & Sons Ltd on behalf of British Society for Plant Pathology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Thatcher, Shawn
Jung, Mark
Panangipalli, Gayathri
Fengler, Kevin
Sanyal, Abhijit
Li, Bailin
Llaca, Victor
Habben, Jeffrey
The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility
title The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility
title_full The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility
title_fullStr The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility
title_full_unstemmed The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility
title_short The NLRomes of Zea mays NAM founder lines and Zea luxurians display presence–absence variation, integrated domain diversity, and mobility
title_sort nlromes of zea mays nam founder lines and zea luxurians display presence–absence variation, integrated domain diversity, and mobility
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257044/
https://www.ncbi.nlm.nih.gov/pubmed/36929631
http://dx.doi.org/10.1111/mpp.13319
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