Gao Dongli, Appiano Michela, Huibers Robin P, Loonen Annelies E H M, Visser Richard G F, Wolters Anne-Marie A, Bai Yuling
Wageningen UR Plant Breeding, Wageningen University, Research Centre, Droevendaalsesteeg 1, 6708PB, Wageningen, the Netherlands.
Mol Plant Pathol. 2015 Jan;16(1):71-82. doi: 10.1111/mpp.12165. Epub 2014 Jul 9.
To screen for potentially novel types of resistance to tomato powdery mildew Oidium neolycopersici, a disease assay was performed on 123 Arabidopsis thaliana accessions. Forty accessions were fully resistant, and one, C24, was analysed in detail. By quantitative trait locus (QTL) analysis of an F2 population derived from C24 × Sha (susceptible accession), two QTLs associated with resistance were identified in C24. Fine mapping of QTL-1 on chromosome 1 delimited the region to an interval of 58 kb encompassing 15 candidate genes. One of these was Enhanced Disease Resistance 1 (EDR1). Evaluation of the previously obtained edr1 mutant of Arabidopsis accession Col-0, which was identified because of its resistance to powdery mildew Golovinomyces cichoracearum, showed that it also displayed resistance to O. neolycopersici. Sequencing of EDR1 in our C24 germplasm (referred to as C24-W) revealed two missing nucleotides in the second exon of EDR1 resulting in a premature stop codon. Remarkably, C24 obtained from other laboratories does not contain the EDR1 mutation. To verify the identity of C24-W, a DNA region containing a single nucleotide polymorphism (SNP) unique to C24 was sequenced showing that C24-W contains the C24-specific nucleotide. C24-W showed enhanced resistance to O. neolycopersici compared with C24 not containing the edr1 mutation. Furthermore, C24-W displayed a dwarf phenotype, which was not associated with the mutation in EDR1 and was not caused by the differential accumulation of pathogenesis-related genes. In conclusion, we identified a natural edr1 mutant in the background of C24.
为筛选对番茄白粉病菌新番茄粉孢菌潜在的新型抗性类型,对123个拟南芥种质进行了病害检测。40个种质完全抗性,对其中一个名为C24的种质进行了详细分析。通过对C24×Sha(感病种质)衍生的F2群体进行数量性状基因座(QTL)分析,在C24中鉴定出两个与抗性相关的QTL。对1号染色体上的QTL-1进行精细定位,将该区域限定在一个58 kb的区间内,包含15个候选基因。其中一个是增强抗病性1(EDR1)。对先前获得的拟南芥Col-0 edr1突变体进行评估,该突变体因其对白粉病菌菊苣白粉菌的抗性而被鉴定,结果表明它对新番茄粉孢菌也表现出抗性。对我们的C24种质(称为C24-W)中的EDR1进行测序,发现在EDR1的第二个外显子中有两个核苷酸缺失,导致提前出现终止密码子。值得注意的是,从其他实验室获得的C24不包含EDR1突变。为验证C24-W的身份,对包含C24特有的单核苷酸多态性(SNP)的DNA区域进行测序,结果表明C24-W包含C24特有的核苷酸。与不包含edr1突变的C24相比,C24-W对新番茄粉孢菌的抗性增强。此外,C24-W表现出矮化表型,这与EDR1突变无关,也不是由病程相关基因的差异积累引起的。总之,我们在C24背景中鉴定出一个天然的edr1突变体。