Abstract:
Apple scab, caused by fungal pathogen Venturia inaequalis, is a severe disease of cultivated apple
(Malus × domestica Borkh.). It is the most studied plant–pathogen interaction of woody plant
species using genetic, genomic, proteomic and bioinformatics approaches in both species. Until
now 17 monogenic resistances against the disease have been identified in different Malus
species and some of them are currently used in scab resistance breeding programs. However,
the evolution of virulent pathogen strains that has ability to overcome the monogenic resistance
raised the need to define new strategies to obtain a durable resistance in apple breeding. Gene
pyramiding becomes a successful method to obtain plants with durable resistance. Recently, the
Rvi5 (Vm) apple scab resistance from the cultivar ‘Murray’ was fine mapped and the region
carrying the resistance was restricted into a region of 1cM flanked by two SSR markers
(FMACH_Vm4 and FMACH_Vm2). In this study, three bacterial artificial chromosome (BAC)
clones spanning the resistance locus were identified, completely sequenced and assembled,
which allowed identifying the putative Rvi5 locus in a region of 154kb in size. The open reading
frame prediction and functional annotation of the identified region revealed the presence of one
putative gene homologous to TMV resistance protein N-like [Malus x domestica] characterized
by a Toll and mammalian interleukin-1 receptor protein nucleotide-binding site leucine-rich
(TNL) repeat structure.
