Division of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi 110012, India.
Chaudhary Charan Singh University, Meerut 250004, UP, India; and Department of Biotechnology, College of Engineering, Daegu University, Gyeongsan City, Gyeongbook 38453, South Korea.
Funct Plant Biol. 2020 Feb;47(3):203-225. doi: 10.1071/FP18336.
Genome-wide transcriptome analysis was undertaken in a leaf-rust resistant bread wheat line CSP44 (selected from Australian cv. Condor) carrying the adult plant resistance (APR) gene Lr48. Two pre-adult plant (P-AP) susceptible stages (S48 and S96) and two adult plant (AP) resistant stages (R48 and R96) were used for RNA-seq. At the susceptible P-AP stage (during S48 to S96), expression increased in 2062 genes, and declined in 130 genes; 1775 of 2062 differentially expressed genes (DEGs) also exhibited high expression during early incompatible stage R48. Comparison of S96 with R96 showed that the expression of 80 genes was enhanced and that of 208 genes declined at the AP stage. At the resistant AP stage (during R48 to R96), expression of mere 25 genes increased and that of 126 genes declined. Apparently, the resistance during late adult stage (R96) is caused by regulation of the expression of relatively fewer genes, although at pre-adult stage (S48 to S96), expression of large number of genes increased; expression of majority of these genes kept on increasing during adult stage at R48 also. These and other results of the present study suggest that APR may mimic some kind of systemic acquired resistance (SAR). The host-specific DEGs belonged to 10 different classes including genes involved in defence, transport, epigenetics, photosynthesis, genes encoding some transcription factors etc. The pathogen (Puccinia triticina) specific DEGs (including three genes encoding known biotrophic effectors) seem to help the pathogen in infection/growth through large-scale stage-specific enhanced expression of host's genes. A putative candidate gene for Lr48 containing protein kinase domain (its ortholog in rice encoding OsWAK8) was also identified.
对携带成株期抗性(APR)基因 Lr48 的抗叶锈面包小麦品系 CSP44(源自澳大利亚 cv. Condor)进行了全基因组转录组分析。使用了两个预成株期(P-AP)感病阶段(S48 和 S96)和两个成株期(AP)抗病阶段(R48 和 R96)进行 RNA-seq。在易感的 P-AP 阶段(S48 到 S96 期间),2062 个基因的表达增加,130 个基因的表达减少;2062 个差异表达基因(DEGs)中有 1775 个在早期不亲和阶段 R48 时也表现出高表达。将 S96 与 R96 进行比较,结果表明,80 个基因的表达增强,208 个基因的表达减少。在抗病的 AP 阶段(R48 到 R96 期间),仅有 25 个基因的表达增加,126 个基因的表达减少。显然,在晚期成株期(R96)的抗性是由相对较少的基因表达调控引起的,尽管在预成株期(S48 到 S96),大量基因的表达增加;在 R48 的成株期,这些基因中的大多数的表达也在持续增加。本研究的这些和其他结果表明,APR 可能模拟某种系统获得性抗性(SAR)。宿主特异性 DEGs 属于 10 个不同类别,包括参与防御、运输、表观遗传学、光合作用、编码某些转录因子等的基因。病原菌(小麦条锈菌)特异性 DEGs(包括三个编码已知生境效应物的基因)似乎通过宿主基因的大规模阶段特异性增强表达,帮助病原菌进行侵染/生长。还鉴定了一个包含蛋白激酶结构域的 Lr48 候选基因(其在水稻中的同源物编码 OsWAK8)。