SMRT-AgRenSeq-d in potato (Solanum tuberosum) identifies candidates for the nematode resistance Gpa5

Author:

Wang YuhanORCID,Brown Lynn HORCID,Adams Thomas MORCID,Cheung Yuk WoonORCID,Li Jie,Young Vanessa,Todd Drummond T,Armstrong Miles RORCID,Neugebauer KonradORCID,Kaur AmanpreetORCID,Harrower Brian,Oome Stan,Wang Xiaodan,Bayer MichaORCID,Hein IngoORCID

Abstract

SummaryPotato is the third most important food crop in the world. Diverse pathogens threaten sustainable crop production but can be controlled, in many cases, through the deployment of disease resistance genes belonging to the family of nucleotide-binding, leucine-rich-repeat (NLR) genes.To identify functional NLRs in established varieties, we have successfully established SMRT-AgRenSeq in tetraploid potatoes and have further enhanced the methodology by including dRenSeq in an approach that we term SMRT-AgRenSeq-d. The inclusion of dRenSeq enables the filtering of candidates after the association analysis by establishing a presence/absence matrix across resistant and susceptible potatoes that is translated into an F1 score. Using a SMRT-RenSeq based sequence representation of the NLRome from the cultivar Innovator, SMRT-AgRenSeq-d analyses reliably identified the late blight resistance benchmark genesR1, R2-like, R3aandR3bin a panel of 117 varieties with variable phenotype penetrations. All benchmark genes were identified with an F1 score of 1 which indicates absolute linkage in the panel.When applied to the elusive nematode disease resistance geneGpa5that controls the Potato Cyst Nematode (PCN) speciesGlobodera pallida(pathotypes Pa2/3), SMRT-AgRenSeq-d identified nine strong candidates. These map to the previously established position on potato chromosome 5 and are potential homologs of the late blight resistance geneR1.Assuming that NLRs are involved in controlling many types of resistances, SMRT-AgRenSeq-d can readily be applied to diverse crops and pathogen systems. In potato, SMRT-AgRenSeq-d lends itself, for example, to further study the elusive PCN resistancesH1orH3for which phenotypic data exist.

Publisher

Cold Spring Harbor Laboratory

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