利用RNA-seq技術篩選藥用野生稻抗白葉枯病相關基因

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

    • 摘要:
      目的  藥用野生稻(Oryza officinalis)屬於稻屬CC染色體組,在長期的自然生存過程中,積累了大量適應惡劣環境的抗性基因。利用轉錄組測序(RNA-seq)挖掘植物抗病相關基因,為開展基因功能與調控機製研究等奠定基礎。
      方法  對雲南省6個居群(Ⅰ~Ⅵ)的38份藥用野生稻進行白葉枯病菌CX28-3和PXO99的抗性評價,以PXO99人工接種處理篩選到的藥用野生稻36號(抗病)與37號(感病)植株為對象,於0、24、48 h取其葉片進行轉錄組測序分析,並預測藥用野生稻抗白葉枯病相關基因。
      結果  6個居群38份雲南藥用野生稻材料對2個菌株(CX28-3和PXO99)表現為不同的抗病性,總體為中抗至抗以上,其中抗病率最高的是Ⅴ居群、為93.50%,最低的是Ⅲ居群、為62.50%。38份藥用野生稻對CX28-3菌株感病的植株有5份,感病率為13.15%;對PXO99菌株的感病率為42.10%,表明PXO99的致病力強。此外,抗2個菌株的藥用野生稻材料有20份,占全部材料的66.67%,37號材料對2個菌株均表現為中感,36號材料對2個菌株都表現為抗。轉錄組測序共鑒定到75 650個差異表達基因(DEGs)。GO功能富集分析顯示,PXO99處理後共包含45個顯著富集的生物進程GO類別,其中富集DEGs數量最多的集中在細胞過程、代謝過程、細胞解剖實體、綁定、催化活性等。KEGG富集分析表明,抗病和感病野生稻材料共顯著富集到19個KEGG通路,其中與抗病相關的蛋白等KEGG通路顯著富集上升,進一步明確抗病藥用野生稻36號的抗病性受白葉枯病菌激發顯著。篩選到共同DEGs 256個,11個基因可能與野生稻白葉枯病抗性密切相關;Unigene1184Unigene15669CL1239CL1421CL4899CL660CL7463 7個基因在抗病材料中上調表達,在感病材料中下調表達;Unigene18206CL210CL3554CL9248 5個基因在抗病材料中下調表達,在感病材料中上調表達。
      結論  6個居群38份雲南藥用野生稻材料對CX-28和PXO99菌株表現出不同的白葉枯病抗性,總體為中抗至抗以上。利用RNA-seq技術獲得與藥用野生稻白葉枯病(PXO99)抗性相關基因11個,可為藥用野生稻抗白葉枯病相關基因的挖掘和功能研究提供參考。

       

      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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