Plant Pathogen Resistance Biotechnology 2016
DOI: 10.1002/9781118867716.ch9
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Problematic Crops: 1. Potatoes

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Cited by 10 publications
(6 citation statements)
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References 81 publications
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“…2012 ). Marker-assisted breeding is then considered efficient for breeding, although R gene activity by functional effector assays seems the best method to distinguish between mechanistically different R genes ( Vleeshouwers et al., 2011b , Jo et al., 2016 ). In this study however, we show that R genes that recognize the same effector (AVR2) can still confer different resistance patterns, which further nuances the strategy to discriminate race-specificity of R genes.…”
Section: Discussionmentioning
confidence: 99%
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“…2012 ). Marker-assisted breeding is then considered efficient for breeding, although R gene activity by functional effector assays seems the best method to distinguish between mechanistically different R genes ( Vleeshouwers et al., 2011b , Jo et al., 2016 ). In this study however, we show that R genes that recognize the same effector (AVR2) can still confer different resistance patterns, which further nuances the strategy to discriminate race-specificity of R genes.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, the modern breeding approach is to isolate a variation of R genes and deploy them in pyramids. This is expected to lead to broad-spectrum recognition of P. infestans isolates and might provide a more durable resistance ( Jo et al. 2016 ).…”
Section: Introductionmentioning
confidence: 99%
“…Currently breeders isolate variants of R genes and deploy them in pyramids or stacks. It is expected that this will result in broad-spectrum recognition of Pi isolates and might provide a more durable resistance in the field (Jo et al, 2016). Recent screening of germplasm has revealed Rpi genes in wild species of Solanum, particularly broadspectrum resistance genes in blb species (Wang et al, 2008(Wang et al, , 2013Hein et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…The Rpi‐ber1.1 and Rpi‐tar1.1 genes were amplified using primers in the promotor and terminator. The resulting PCR fragments were cloned into pBINPLUS‐PASSA (Jo et al , 2016 ) and were expressed in transgenic Desiree plants under the control of their native regulatory elements. For transient expression analyses, the coding sequences of the allelic variants were cloned under the Rpi‐chc1.1 regulatory elements (900‐bp promotor and 400‐bp terminator) into pDEST using a multisite gateway protocol.…”
Section: Methodsmentioning
confidence: 99%