利用RNA-seq技术筛选药用野生稻抗白叶枯病相关基因

    Screening of Genes Related to Resistance to Bacterial Leaf Blight in Oryza officinalis by using RNA-seq Technology

    • 摘要:
      目的  药用野生稻(Oryza officinalis)属于稻属CC染色体组,在长期的自然生存过程中,积累了大量适应恶劣环境的抗性基因。利用转录组测序(RNA-seq)挖掘植物抗病相关基因,为开展基因功能与调控机制研究等奠定基础。
      方法  对云南省6个居群(Ⅰ~Ⅵ)的38份药用野生稻进行白叶枯病菌CX28-3和PXO99的抗性评价,以PXO99人工接种处理筛选到的药用野生稻36号(抗病)与37号(感病)植株为对象,于0、24、48 h取其叶片进行转录组测序分析,并预测药用野生稻抗白叶枯病相关基因。
      结果  6个居群38份云南药用野生稻材料对2个菌株(CX28-3和PXO99)表现为不同的抗病性,总体为中抗至抗以上,其中抗病率最高的是Ⅴ居群、为93.50%,最低的是Ⅲ居群、为62.50%。38份药用野生稻对CX28-3菌株感病的植株有5份,感病率为13.15%;对PXO99菌株的感病率为42.10%,表明PXO99的致病力强。此外,抗2个菌株的药用野生稻材料有20份,占全部材料的66.67%,37号材料对2个菌株均表现为中感,36号材料对2个菌株都表现为抗。转录组测序共鉴定到75 650个差异表达基因(DEGs)。GO功能富集分析显示,PXO99处理后共包含45个显著富集的生物进程GO类别,其中富集DEGs数量最多的集中在细胞过程、代谢过程、细胞解剖实体、绑定、催化活性等。KEGG富集分析表明,抗病和感病野生稻材料共显著富集到19个KEGG通路,其中与抗病相关的蛋白等KEGG通路显著富集上升,进一步明确抗病药用野生稻36号的抗病性受白叶枯病菌激发显著。筛选到共同DEGs 256个,11个基因可能与野生稻白叶枯病抗性密切相关;Unigene1184Unigene15669CL1239CL1421CL4899CL660CL7463 7个基因在抗病材料中上调表达,在感病材料中下调表达;Unigene18206CL210CL3554CL9248 5个基因在抗病材料中下调表达,在感病材料中上调表达。
      结论  6个居群38份云南药用野生稻材料对CX-28和PXO99菌株表现出不同的白叶枯病抗性,总体为中抗至抗以上。利用RNA-seq技术获得与药用野生稻白叶枯病(PXO99)抗性相关基因11个,可为药用野生稻抗白叶枯病相关基因的挖掘和功能研究提供参考。

       

      Abstract:
      Objective  Oryza officinalis belongs to the CC chromosome group of rice genus, and it had accumulated a large number of resistance genes that adapt to harsh environments during long-term natural survival. Based on transcriptome sequencing (RNA-seq), disease resistance related genes could be discovered, laying a foundation for researches on gene function and regulatory mechanisms.
      Methods  Two isolates of Xanthomonas oryzae pv. oryzae CX28-3 and PXO99 were inoculated to 38 O. officinalis wild rice materials of 6 populations (Ⅰ-Ⅵ) from Yunnan Province, and different resistance phenotypes were evaluated. The highly resistant and susceptible populations were selected for transcriptome sequencing. The transcriptome sequencing data of O. officinalis 36 (resistant) and O. officinalis 37 (susceptible) plants after PXO99 inoculation stress at 0, 24, and 48 h were analyzed. And genes related to resistance to bacterial leaf blight in O. officinalis wild rice were predicted.
      Results  The 38 O. officinalis wild rice materials from 6 populations showed different disease resistance to 2 strains (CX28-3 and PXO99), and the overall resistance rate was medium or above, among which the highest resistance rate was 93.50% in Ⅴ population and the lowest rate was 62.50% in Ⅲ population. Among them, it was found that 5 accessions of O.officinalis were susceptible to CX28-3 isolate, with a disease infection rate of 13.15%, and 42.10% to PXO99 strain, indicating that PXO99 had strong pathogenicity. There were 20 O. officinalis materials resistant to two strains simultaneously, accounting for 66.67% of all materials. O. officinalis 37 showed moderate susceptibility to both strains, while O. officinalis 36 showed resistance to both strains. Through transcriptome sequencing of O. officinalis 36 and 37 plants, a total of 75 650 differentially expressed genes (DEGs) were identified. GO functional enrichment analysis revealed that PXO99 treatment resulted in a total of 45 significantly enriched GO categories in biological processes. Among them, the most enriched DEGs were concentrated in cellular processes, metabolic processes, cellular anatomical entities, binding, catalytic activity, etc. KEGG enrichment analysis showed that 19 KEGG pathways were significantly enriched in the resistant and susceptible O. officinalis materials, among which KEGG pathways related to disease resistance to proteins were significantly enriched and increased. This further clarified that the resistance to disease of the O. officinalis 36 was significantly stimulated by the Xanthomonas oryzae pv. oryzae. A total of 256 common DEGs were screened, and 11 genes were closely related to the resistance to bacterial leaf blight in O. officinalis; Unigene1184, Unigene15669, CL1239, CL1421, CL4899, CL660, and CL7463 genes were up-regulated in resistant materials and down-regulated in susceptible materials. Unigene18206, CL210, CL3554, and CL9248 genes were down-regulated in resistant materials and up-regulated in susceptible materials.
      Conclusion  38 accessions of O. officinalis of 6 populations from Yunnan showed different disease resistances to two strains (CX-28 and PXO99), but overall resistance was moderate or above. By using transcriptome sequencing technology, 11 genes related to resistance to bacterial leaf blight in O. officinalis were obtained. The research results will provide references for the exploration and functional study of genes related to resistance to bacterial leaf blight in O. officinalis.

       

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