Abstract

BackgroundThe development of CRISPR/Cas9 technology has facilitated targeted mutagenesis in an efficient and precise way. Previously, RNAi silencing of the susceptibility (S) gene PowderyMildewResistance 4 (PMR4) in tomato has been shown to enhance resistance against the powdery mildew pathogen Oidium neolycopersici (On).ResultsTo study whether full knock-out of the tomato PMR4 gene would result in a higher level of resistance than in the RNAi-silenced transgenic plants we generated tomato PMR4 CRISPR mutants. We used a CRISPR/Cas9 construct containing four single-guide RNAs (sgRNAs) targeting the tomato PMR4 gene to increase the possibility of large deletions in the mutants. After PCR-based selection and sequencing of transformants, we identified five different mutation events, including deletions from 4 to 900-bp, a 1-bp insertion and a 892-bp inversion. These mutants all showed reduced susceptibility to On based on visual scoring of disease symptoms and quantification of relative fungal biomass. Histological observations revealed a significantly higher occurrence of hypersensitive response-like cell death at sites of fungal infection in the pmr4 mutants compared to wild-type plants. Both haustorial formation and hyphal growth were diminished but not completely inhibited in the mutants.ConclusionCRISPR/Cas-9 targeted mutagenesis of the tomato PMR4 gene resulted in mutants with reduced but not complete loss of susceptibility to the PM pathogen On. Our study demonstrates the efficiency and versatility of the CRISPR/Cas9 system as a powerful tool to study and characterize S-genes by generating different types of mutations.

Highlights

  • The development of clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology has facilitated targeted mutagenesis in an efficient and precise way

  • We used four Single-guide RNA (sgRNA) in order to increase the chances of obtaining mutants with large deletions [29, 30]

  • Powdery Mildew Resistance 4 (PMR4) contains two known protein domains according to NCBI Conserved Domains: FKS1dom1 [32] and the Glucan-synthase domain [33]

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Summary

Introduction

The development of CRISPR/Cas technology has facilitated targeted mutagenesis in an efficient and precise way. Santillán Martínez et al BMC Plant Biology (2020) 20:284 In addition to these dominantly-inherited resistance genes a recessive gene named ol-2 was identified [7]. This is a loss-of-function mutant allele of the powdery mildew susceptibility (S) gene, MILDEW RESISTANCE LOCUS O (MLO) [7]. In homozygous state this ol-2 allele confers broad-spectrum resistance to different PM species by inducing papilla formation and callose deposition, which block fungal development at penetration stage [6]. The use of such S genes in plant breeding, due to their broad-spectrum and potentially durable resistance characteristics, represent a promising alternative to the introgression of R genes that has been driving traditional resistance breeding [9,10,11]

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