Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene
Chrysanthemum are important perennial commercial and ornamental flowers worldwide. Chrysanthemum white rust caused by the fungus Puccinia horiana is a destructive disease. Recent studies have aimed to identify sources of resistance to this disease, whereas genes related to the resistance to the fung...
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Maximum Academic Press
2023-01-01
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Series: | Ornamental Plant Research |
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Online Access: | https://www.maxapress.com/article/doi/10.48130/OPR-2023-0007 |
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author | Lin Jiang Xin Feng Xinyue Chen Yumeng Yu Hongyu Mao Pengfang Zhu |
author_facet | Lin Jiang Xin Feng Xinyue Chen Yumeng Yu Hongyu Mao Pengfang Zhu |
author_sort | Lin Jiang |
collection | DOAJ |
description | Chrysanthemum are important perennial commercial and ornamental flowers worldwide. Chrysanthemum white rust caused by the fungus Puccinia horiana is a destructive disease. Recent studies have aimed to identify sources of resistance to this disease, whereas genes related to the resistance to the fungus were rarely reported. In this study, we used highly resistant and susceptible chrysanthemum cultivars whose disease sensitivity was confirmed over years of observation. Using a conserved nucleotide binding site (NBS) domain sequence that is associated with resistance to rust in other plants as a query in a BLAST search against the chrysanthemum reference database, we identified the gene CHR00059759. There were eight consistent nonsynonymous mutations between the highly resistant and susceptible cultivars, five of which occurred in the NB-ARC conserved domain. The expression level of CmCC-NB-ARC increased and then decreased in the susceptible cultivar 'LZ08-61', whereas decreased and then increased in the resistant cultivar 'C029' in the eight time-points after inoculation with the fungus. In order to verify the gene function, we constructed an overexpression vector 35Spro:CmCC-NB-ARC and transformed into the susceptible cultivar 'Jinba'. Compared with 'Jinba', the relative expression levels of the gene in the transgenic plants increased significantly at 48h after inoculation. Compared with three overexpression lines, the diseased spots appeared in 'Jinba' at 15d after inoculation. Hence, we speculated the gene CmCC-NB-ARC conferred resistance to chrysanthemum white rust. This study provides insight into the mechanism of resistance to chrysanthemum white rust and might help inform the breeding of resistant cultivars. |
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spelling | doaj.art-f879a65a7d5a43229462e0a701c4c8c72024-02-28T01:52:56ZengMaximum Academic PressOrnamental Plant Research2769-20942023-01-01311910.48130/OPR-2023-0007OPR-2023-0007Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance geneLin Jiang0Xin Feng1Xinyue Chen2Yumeng Yu3Hongyu Mao4Pengfang Zhu5College of Forestry, Shenyang Agricultural University, Shenyang 110866, ChinaCollege of Forestry, Shenyang Agricultural University, Shenyang 110866, ChinaCollege of Forestry, Shenyang Agricultural University, Shenyang 110866, ChinaCollege of Forestry, Shenyang Agricultural University, Shenyang 110866, ChinaCollege of Forestry, Shenyang Agricultural University, Shenyang 110866, ChinaCollege of Forestry, Shenyang Agricultural University, Shenyang 110866, ChinaChrysanthemum are important perennial commercial and ornamental flowers worldwide. Chrysanthemum white rust caused by the fungus Puccinia horiana is a destructive disease. Recent studies have aimed to identify sources of resistance to this disease, whereas genes related to the resistance to the fungus were rarely reported. In this study, we used highly resistant and susceptible chrysanthemum cultivars whose disease sensitivity was confirmed over years of observation. Using a conserved nucleotide binding site (NBS) domain sequence that is associated with resistance to rust in other plants as a query in a BLAST search against the chrysanthemum reference database, we identified the gene CHR00059759. There were eight consistent nonsynonymous mutations between the highly resistant and susceptible cultivars, five of which occurred in the NB-ARC conserved domain. The expression level of CmCC-NB-ARC increased and then decreased in the susceptible cultivar 'LZ08-61', whereas decreased and then increased in the resistant cultivar 'C029' in the eight time-points after inoculation with the fungus. In order to verify the gene function, we constructed an overexpression vector 35Spro:CmCC-NB-ARC and transformed into the susceptible cultivar 'Jinba'. Compared with 'Jinba', the relative expression levels of the gene in the transgenic plants increased significantly at 48h after inoculation. Compared with three overexpression lines, the diseased spots appeared in 'Jinba' at 15d after inoculation. Hence, we speculated the gene CmCC-NB-ARC conferred resistance to chrysanthemum white rust. This study provides insight into the mechanism of resistance to chrysanthemum white rust and might help inform the breeding of resistant cultivars.https://www.maxapress.com/article/doi/10.48130/OPR-2023-0007cc-nb-arc conserved domainchrysanthemumpuccinia horianaoverexpression |
spellingShingle | Lin Jiang Xin Feng Xinyue Chen Yumeng Yu Hongyu Mao Pengfang Zhu Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene Ornamental Plant Research cc-nb-arc conserved domain chrysanthemum puccinia horiana overexpression |
title | Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene |
title_full | Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene |
title_fullStr | Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene |
title_full_unstemmed | Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene |
title_short | Cloning and identification of CmCC-NB-ARC, a chrysanthemum white rust resistance gene |
title_sort | cloning and identification of cmcc nb arc a chrysanthemum white rust resistance gene |
topic | cc-nb-arc conserved domain chrysanthemum puccinia horiana overexpression |
url | https://www.maxapress.com/article/doi/10.48130/OPR-2023-0007 |
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