枝孢菌SYC23中重寄生相关转录因子基因挖掘及表达分析OA
Genome-wide identification and expression analysis of mycoparasitic transcription factors in Cladosporium anthropophilum SYC23
[目的]挖掘与枝孢菌(Cladosporium anthropophilum)SYC23重寄生相关的MYB和bHLH家族基因,明确其数目及在重寄生过程中发挥的作用,为进一步研究枝孢菌SYC23的重寄生机制提供理论基础.[方法]本研究利用生物信息学方法对菌株SYC23基因组进行转录因子MYB和bHLH家族基因挖掘与分析,并利用RT-qPCR对其在锈孢子诱导下的表达情况进行检测.[结果]共鉴定出6个MYB和2个bHLH家族基因,分别命名为CaMYB1~CaMYB6及CabHLH1~CabHLH2.6个MYB转录因子都含有SANT保守结构域,2个bHLH转录因子都含有HLH结构域.8个转录因子的分子质量为49.25~155.66 ku,等电点为4.75~9.90,均为亲水蛋白;除CaMYB5基因定位于线粒体,其余均定位于细胞核,均含有响应病原菌的启动子结合位点.RT-qPCR定量结果显示,在锈孢子诱导初期,8个转录因子相对表达量差异不明显;CaMYB3和CaMYB5两个基因在24 h表达量呈下调趋势,但在48~72 h时的表达量相较于0 h显著增加,且CaMYB4基因在72 h时的表达量约为0 h的37.5倍.说明CaMYBs和CabHLHs基因可能在锈孢子诱导中后期参与枝孢菌SYC23的胁迫调控作用,且在锈孢子诱导后48 h时大量响应真菌侵染过程.[结论]在枝孢菌SYC23中成功挖掘鉴定得到8个与重寄生相关的MYB和bHLH转录因子.
[Objective]Identification of MYB and bHLH family genes associated with the mycoparasitism of Cladosporium anthropo-philum SYC23 and clarification on their numbers and roles in the mycoparasitic process were carried out,to provide a theoretical ba-sis for further research on the mycoparasitic mechanism of strain SYC23.[Method]Bioinformatics methods were applied to identify and analyze the genes of transcription factors MYB and bHLH families in the genome of strain SYC23,and then RT-qPCR was used to detect their expressions under rust spore induction.[Result]A total of 6 MYB and 2 bHLH family genes were identified,which were named CaMYB1-CaMYB6 and CabHLH1-CabHLH2.All the 6 CaMYBs genes contained a SANT conserved domain,and the 2 CabHLHs contained a HLH domain,respectively.All the 8 transcription factors were hydrophilic proteins with molecular weights of 49.25-155.66 ku,and theoretical isoelectric points of 4.75-9.90.Except for CaMYB5 which was located in the mitochondria,the rest were all located in the nucleus,and all contained promoter binding sites corresponding to pathogenic bacteria.RT-qPCR results revealed that there was no significant difference in the expressions of the 8 transcription factor genes at the early stage of rust spore induction;at 24 h after the induction,the relative expression levels of CaMYB3 and CaMYB5 genes were down-regulated,however,at 48-72 h after the induction,their expression levels were significantly higher in comparison to those at 0 h,especially the expres-sion level of CaMYB4 gene at 72 h,which was approximately 37.5-fold greater.The expression patterns unveiled the functions of CaMYBs and CabHLHs genes in the stress regulation of strain SYC23 in the middle to late stages of rust spore induction,and respon-ded in large quantities to fungal infection at 48 h after rust spore induction.[Conclusion]A total of 8 MYB and bHLH transcription factors which were related to mycoparasitism were successfully mined and identified in C.anthropophilum SYC23.
李明娇;严梦玲;汤艳萍;陈晨;李进秋;高若天;李靖
西南林业大学生物与食品工程学院,云南 昆明 650224西南林业大学生物与食品工程学院,云南 昆明 650224西南林业大学生物与食品工程学院,云南 昆明 650224西南林业大学生物与食品工程学院,云南 昆明 650224西南林业大学生物与食品工程学院,云南 昆明 650224西南林业大学生物与食品工程学院,云南 昆明 650224西南林业大学生物与食品工程学院,云南 昆明 650224
农业科技
枝孢菌SYC23MYB转录因子bHLH转录因子RT-qPCR重寄生机制
Cladosporium anthropophilum SYC23MYB transcription factorbHLH transcription factorRT-qPCRmycoparasitism
《福建农林大学学报(自然科学版)》 2026 (2)
257-268,12
云南省农业基础研究专项重点项目(202301BD07000-159).
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