Transcriptomics Laboratory (K-Lab), Division of Plant Biotechnology, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir, Shalimar, Srinagar, J&K, 190025, India.
NAHEP, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir, Shalimar, Srinagar, J&K, 190025, India.
Funct Integr Genomics. 2022 Dec;22(6):1315-1330. doi: 10.1007/s10142-022-00889-x. Epub 2022 Aug 5.
Apple scab is caused by an ascomycete fungus, Venturia inaequalis (Cke.) Wint., which is one of the most severe disease of apple (Malus × Domestica Borkh.) worldwide. The disease results in 30-40% fruit loss annually and even complete loss in some places. Owing to the evolving susceptibility of resistant apple genotypes harboring R-genes to new variants of V. inaequalis, a comparative transcriptome analysis using Illumina (HiSeq) platform of three scab-resistant (Florina, Prima, and White Dotted Red) and three susceptible (Ambri, Vista Bella, and Red Delicious) apple genotypes was carried out to mine new scab resistance genes. The study led to the identification of 822 differentially expressed genes in the tested scab-resistant and scab-susceptible apple genotypes. The most upregulated genes uniformly expressed in resistant varieties compared to susceptible ones were those coding for 17.3 kDa class II heat shock protein-like, chaperone protein ClpB1, glutathione S-transferase L3-like protein, B3 domain-containing protein At3g18960-like, transcription factor bHLH7, zinc finger MYM-type protein 1-like, and nine uncharacterized proteins, besides three lncRNAs. The genes that were downregulated in susceptible and upregulated in resistant cultivars were those coding for non-specific lipid transfer protein GPI-anchored 1, rust resistance kinase Lr10-like, disease resistance protein RPS6-like, and many uncharacterized proteins. DESeq2 analysis too revealed 20 DEGs that were upregulated in scab-resistant cultivars. Furthermore, a total of 361 genes were significantly upregulated in scab-susceptible variety, while 461 were found downregulated (P value < 0.05 and Log2 (FC) > 1). The differentially expressed genes (DEGs) were related to various pathways, i.e., metabolic, protein processing, biosynthesis of secondary metabolites, plant hormone signal transduction, autophagy, ubiquitin-mediated proteolysis, plant-pathogen interaction, lipid metabolism, and protein modification pathways. Real-time expression of a set of selected twelve DEGs further validated the results obtained from RNA-seq. Overall, these findings lay the foundation for investigating the genetic basis of apple scab resistance and defense pathways that might have a plausible role in governing scab resistance in apple against V. inaequalis.
苹果黑星病是由子囊菌真菌苹果黑星菌(Venturia inaequalis(Cke.)Wint.)引起的,是全球范围内苹果最严重的病害之一。该病害每年导致 30-40%的果实损失,在某些地区甚至会导致完全减产。由于具有 R 基因的抗性苹果基因型对苹果黑星菌新变体的敏感性不断演变,因此使用 Illumina(HiSeq)平台对三个抗黑星病(Florina、Prima 和 White Dotted Red)和三个易感(Ambri、Vista Bella 和 Red Delicious)的苹果基因型进行了比较转录组分析,以挖掘新的黑星病抗性基因。该研究在测试的抗黑星病和易感苹果基因型中鉴定出 822 个差异表达基因。与易感品种相比,在抗性品种中均匀表达的上调基因是编码 17.3 kDa 类 II 热休克蛋白样、伴侣蛋白 ClpB1、谷胱甘肽 S-转移酶 L3 样蛋白、B3 结构域包含蛋白 At3g18960 样、转录因子 bHLH7、锌指 MYM 型蛋白 1 样和九个未鉴定蛋白的基因,此外还有三个 lncRNA。在易感品种中下调而在抗性品种中上调的基因是编码非特异性脂质转移蛋白 GPI-锚定 1、锈病抗性激酶 Lr10 样、抗性蛋白 RPS6 样和许多未鉴定蛋白的基因。DESeq2 分析也揭示了在抗黑星病品种中上调的 20 个差异表达基因。此外,在易感品种中,共有 361 个基因显著上调,而 461 个基因下调(P 值<0.05,Log2(FC)>1)。差异表达基因(DEGs)与各种途径相关,即代谢、蛋白质加工、次生代谢物生物合成、植物激素信号转导、自噬、泛素介导的蛋白水解、植物-病原体相互作用、脂质代谢和蛋白修饰途径。对一组选定的 12 个 DEG 的实时表达进一步验证了 RNA-seq 获得的结果。总的来说,这些发现为研究苹果黑星病抗性的遗传基础和防御途径奠定了基础,这些途径可能在控制苹果对苹果黑星菌的抗性方面发挥重要作用。