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Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12
BACKGROUND: Pathogen avirulence (Avr) genes can evolve rapidly when challenged by the widespread deployment of host genes for resistance. They can be effectively isolated by positional cloning provided a robust and well-populated genetic map is available. RESULTS: An updated, SSR-based physical map...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984427/ https://www.ncbi.nlm.nih.gov/pubmed/29855268 http://dx.doi.org/10.1186/s12866-018-1192-x |
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author | Li, Tonghui Wen, Jianqiang Zhang, Yaling Correll, James Wang, Ling Pan, Qinghua |
author_facet | Li, Tonghui Wen, Jianqiang Zhang, Yaling Correll, James Wang, Ling Pan, Qinghua |
author_sort | Li, Tonghui |
collection | PubMed |
description | BACKGROUND: Pathogen avirulence (Avr) genes can evolve rapidly when challenged by the widespread deployment of host genes for resistance. They can be effectively isolated by positional cloning provided a robust and well-populated genetic map is available. RESULTS: An updated, SSR-based physical map of the rice blast pathogen Magnaporthe oryzae (Mo) has been constructed based on 116 of the 120 SSRs used to assemble the last map, along with 18 newly developed ones. A comparison between the two versions of the map has revealed an altered marker content and order within most of the Mo chromosomes. The avirulence gene AvrPi12 was mapped in a population of 219 progeny derived from a cross between the two Mo isolates CHL42 and CHL357. A bulked segregant analysis indicated that the gene was located on chromosome 6, a conclusion borne out by an analysis of the pattern of segregation shown by individual isolates. Six additional PCR-based markers were developed to improve the map resolution in the key region. AvrPi12 was finally located within the sub-telomeric region of chromosome 6, distal to the SSR locus LSM6–5. CONCLUSIONS: The improved SSR-based linkage map should be useful as a platform for gene mapping and isolation in Mo. It was used to establish the location of AvrPi12, thereby providing a starting point for its positional cloning. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1192-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5984427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59844272018-06-07 Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 Li, Tonghui Wen, Jianqiang Zhang, Yaling Correll, James Wang, Ling Pan, Qinghua BMC Microbiol Research Article BACKGROUND: Pathogen avirulence (Avr) genes can evolve rapidly when challenged by the widespread deployment of host genes for resistance. They can be effectively isolated by positional cloning provided a robust and well-populated genetic map is available. RESULTS: An updated, SSR-based physical map of the rice blast pathogen Magnaporthe oryzae (Mo) has been constructed based on 116 of the 120 SSRs used to assemble the last map, along with 18 newly developed ones. A comparison between the two versions of the map has revealed an altered marker content and order within most of the Mo chromosomes. The avirulence gene AvrPi12 was mapped in a population of 219 progeny derived from a cross between the two Mo isolates CHL42 and CHL357. A bulked segregant analysis indicated that the gene was located on chromosome 6, a conclusion borne out by an analysis of the pattern of segregation shown by individual isolates. Six additional PCR-based markers were developed to improve the map resolution in the key region. AvrPi12 was finally located within the sub-telomeric region of chromosome 6, distal to the SSR locus LSM6–5. CONCLUSIONS: The improved SSR-based linkage map should be useful as a platform for gene mapping and isolation in Mo. It was used to establish the location of AvrPi12, thereby providing a starting point for its positional cloning. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1192-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-31 /pmc/articles/PMC5984427/ /pubmed/29855268 http://dx.doi.org/10.1186/s12866-018-1192-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Li, Tonghui Wen, Jianqiang Zhang, Yaling Correll, James Wang, Ling Pan, Qinghua Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 |
title | Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 |
title_full | Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 |
title_fullStr | Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 |
title_full_unstemmed | Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 |
title_short | Reconstruction of an SSR-based Magnaporthe oryzae physical map to locate avirulence gene AvrPi12 |
title_sort | reconstruction of an ssr-based magnaporthe oryzae physical map to locate avirulence gene avrpi12 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984427/ https://www.ncbi.nlm.nih.gov/pubmed/29855268 http://dx.doi.org/10.1186/s12866-018-1192-x |
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