雪岭云杉响应畸形金锈菌侵染的转录组学分析OA
Transcriptome analysis of Picea schrenkiana to infection by Chrysomyxa deformans
[目的]开展雪岭云杉响应畸形金锈菌侵染的转录组学分析,为探究其致病分子机制奠定基础.[方法]以雪岭云杉当年生感病和健康嫩梢为材料,应用 RNA-Seq 测序技术,挖掘雪岭云杉响应锈病侵染的关键基因,初步探究雪岭云杉-锈病互作过程中关键基因表达、信号通路及代谢途径.[结果]1)转录组测序共检测到3 461 个差异表达基因(Differentially expressed genes,DEGs),其中1 658 个DEGs 上调表达,1 803 个DEGs 下调表达;2)GO 富集分析发现,DEGs 主要富集在转移酶活性、转移糖基团、血红素结合、四吡咯结合、ADP 结合、辅酶结合、铁离子结合、UDP-糖基转移酶活性、氧化还原酶活性等通路;3)KEGG 分析发现,DEGs 共注释到 124 条 KEGG 通路,代谢途径类目最多,差异基因显著富集在苯丙烷生物合成、类黄酮生物合成、谷胱甘肽代谢、亚油酸代谢、肌醇磷酸代谢途径中;4)萜类合成酶相关基因 LOC131073238、TPS-1,8cin、TPS-Lin-2、PT5(novel.5099)、PT5(novel.5096)下调表达,LOC131042632、ag5 上调表达,差异基因 LOC131042632、LOC131073238、TPS-1,8cin 富集在二萜类生物合成通路;5)苯丙烷生物合成途径中,差异基因 CYP71AU50、PER12、PER53、PER65、4CL、UGT84A2、CCL7 下调表达,36 个差异基因上调表达.[结论]雪岭云杉可能通过萜类生物合成通路和苯丙烷生物合成通路中关键酶活性的变化响应畸形金锈菌的侵染.
[Objective]This study conducted a transcriptomic analysis of in response to C.deformans infection in Picea schrenkiana,laying the foundation for future research into the molecular pathogenic mechanisms of C.deformans pathogenicity.[Method]Using RNA-Seq technology to compare diseased and healthy current-year tissues of P.schrenkiana,this study explored the key genes,signaling pathways,and metabolic pathways involved in the P.schrenkiana-C.deformans interaction.[Result]1)Transcriptome sequencing identifies 3 461 differentially expressed genes(DEGs),including 1 658 upregulated and 1 803 downregulated genes;2)GO analysis shows that DEGs are mainly enriched in terms like transferase activity,sugar group transfer,heme binding,tetrapyrrole binding,ADP binding,coenzyme binding,iron ion binding,UDP-glycosyltransferase activity,and oxidoreductase activity;3)KEGG analysis finds DEGs annotated in 124 KEGG pathways,with the most in metabolic pathways.DEGs are notably enriched in phenylpropanoid biosynthesis,flavonoid biosynthesis,glutathione metabolism,linoleic acid metabolism,and inositol phosphate metabolism pathways;4)Terpene synthase-related genes LOC131073238,TPS-1,8cin,TPS-Lin-2,PT5(novel.5099)and PT5(novel.5096)are downregulated,while LOC131042632 and ag5 are upregulated.Notably,DEGs LOC131042632,LOC131073238,and TPS-1,8cin are enriched in diterpenoid biosynthesis pathways;5)In the phenylpropanoid biosynthesis pathway,DEGs CYP71AU50,PER12,PER53,PER65,4CL,UGT84A2,and CCL7 are downregulated,while 36 DEGs are upregulated.[Conclusion]P.schrenkiana may respond to rust infection through strategies such as lignin synthesis,terpenoid compound production,and modulation of signaling transduction capabilities.
赛牙热木·哈力甫;刘国蓉;张思佳;李创新;刘闻慧;邓勋
石河子大学,新疆 石河子 832003石河子大学,新疆 石河子 832003石河子大学,新疆 石河子 832003石河子大学,新疆 石河子 832003石河子大学,新疆 石河子 832003黑龙江省森林保护研究所,黑龙江 哈尔滨 150040
农业科技
雪岭云杉锈病畸形金锈菌转录组
Picea schrenkianarust diseasesChrysomyxa deformanstranscriptome
《中南林业科技大学学报》 2026 (4)
139-148,208,11
国家自然科学基金项目(31670649)黑龙江省自然科学基金项目(LH2023C105)黑龙江省重点研发项目(2023ZX02B05)石河子大学高层次人才科研启动项目(RCZK2021B23)石河子大学自主资助支持专项(ZZZC2022009).
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