In-vitro anti-fungal assay and association analysis reveal a role for the Pinus monticola PR10 gene (PmPR10-3.1) in quantitative disease resistance to white pine blister rust

被引:7
|
作者
Liu, Jun-Jun [1 ]
Fernandes, Humberto [2 ,5 ]
Zamany, Arezoo [1 ]
Sikorski, Michal [3 ]
Jaskolski, Mariusz [2 ,3 ]
Sniezko, Richard A. [2 ,3 ,4 ]
机构
[1] Nat Resources Canada, Canadian Forest Serv, Victoria, BC, Canada
[2] Polish Acad Sci, Inst Bioorgan Chem, Poznan, Poland
[3] Adam Mickiewicz Univ, Fac Chem, Dept Crystallog, Poznan, Poland
[4] USDA ARS, Dorena Genet Resource Ctr, Cottage Grove, OR USA
[5] Polish Acad Sci, Int Ctr Translat Eye Res, Inst Phys Chem, Warsaw, Poland
关键词
association analysis; in-vitro anti-fungal array; pathogenesis-related protein family 10; quantitative disease resistance; white pine blister rust; PATHOGENESIS-RELATED PROTEIN; SOUTHERN LEAF-BLIGHT; PR-10; EXPRESSION; BINDING; FUNGAL; STRESS; RIBONUCLEASE; CHITINASE; SOFTWARE;
D O I
10.1139/gen-2020-0080
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Pathogenesis-related (PR) proteins play important roles in plant defense response. However, functional investigation of PR10 genes is still limited and their physiological roles have not been conclusively characterized in biological processes of conifer trees. Here, we identified multiple novel members in the western white pine (Pinus monticola) PmPR10 family by bioinformatic mining available transcriptomic data. Phylogenetic analysis of protein sequences revealed four PR10 and two PR10-like clusters with a high synteny across different species of five-needle pines. Of 10 PmPR10 genes, PmPR10-3.1 was selected and expressed in Escherichia coli. The purified recombinant protein exhibited inhibitory effects on spore hyphal growth of fungal pathogens Cronartium ribicola, Phoma exigua, and Phoma argillacea by in-vitro anti-fungal analysis. Genetic variation analysis detected a total of 21 single nucleotide polymorphisms (SNPs) within PmPR10-3.1 in a collection of P. monticola seed families. A nonsynonymous SNP (t178g) showed significant association with relative levels of quantitative disease resistance (QDR), explaining about 8.7% of phenotypic variation as the peak value across all SNPs. Our results provide valuable insight into the genetic architecture underlying P. monticola QDR and imply that PmPR10-3.1 may function as an important component in conifer basal immunity for non-specific resistance to a wide spectrum of pathogens.
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页码:693 / 704
页数:12
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