玉米大斑病菌小分子热激蛋白基因克隆与表达分析OA北大核心CSTPCD
Cloning and Expression Analysis of Genes of Small Heat Shock Protein in Setosphaeria turcica
[目的]克隆玉米大斑病菌(Setosphaeria turcica)小分子热激蛋白(small heat shock protein,sHSP)基因,分析其结构及在病菌发育和HT-毒素诱导过程中的表达模式.[方法]利用隐马尔可夫模型(hidden Markov model,HMM)筛选玉米大斑病菌全基因组范围内的sHSP家族成员,采用PCR技术克隆玉米大斑病菌 01-23 菌株的sHSP,通过生物信息学方法进行sHSP的理化性质分析、亚细胞定位、结构预测和系统发育分析,RNA-Seq和RT-qPCR分析sHSP在玉米大斑病菌不同发育阶段和HT-毒素诱导过程中的表达情况.[结果]从玉米大斑病菌基因组筛选到 3 个sHSP家族成员(StHSP37.2、StHSP37.0 和StHSP22.6),克隆了 01-23 菌株中 3 个sHSP的DNA序列,编码的sHSP蛋白均属于弱酸、亲水蛋白,无跨膜结构域和信号肽;二级结构中无规则卷曲占 58.97%—60.35%,而β-转角仅为 2.69%—7.83%;亚细胞定位预测StHSP37.2和 StHSP37.0 位于细胞核,而 StHSP22.6 位于细胞核和细胞质;均含有近 C 端的 ACD_sHSP-like 结构域,StHSP37.2、StHSP37.0 和StHSP22.6 分别有 2、3 和 5 个保守基序;利用SWISS-Model和AlphaFill构建了sHSP单体的三级结构模型;系统发育分析结果表明,StHSP22.6 与链格孢(Alternaria alternata)、StHSP37.2 和 StHSP37.0 与玉米小斑病菌(Bipolaris maydis)的sHSP亲缘关系较近;玉米大斑病菌sHSP在菌丝中表达量最高,其次为芽管、附着胞和侵入钉,在分生孢子中表达量最低;StHSP22.6和StHSP37.2与玉米大斑病菌HT-毒素诱导显著负相关,在 14 d时相对基因表达量分别上调 6.45 和 18.12 倍,21、28 d时StHSP37.2表达量仅上调 2.56、1.78 倍,而StHSP22.6表达量与WT无显著差异;StHSP37.0与HT-毒素诱导显著正相关,14、21 和 28 d时相对基因表达量分别下调 59.23%、86.30%和 88.11%;通过与玉米大斑病菌sHSP显著相关的表达基因挖掘,推测StHSP37.2 和StHSP22.6 主要与HSP90、HSP104、分解代谢及线粒体Mg2+转运有关,而StHSP37.0 主要与液泡碱性氨基酸转运、有机合成和分泌有关.[结论]玉米大斑病菌sHSP家族成员既具有高度保守性,又与其他sHSP有结构和系统发育的差异性;不仅与玉米大斑病菌菌丝、芽管、附着胞和侵入钉发育相关,在HT-毒素诱导过程中也发挥重要调控作用.
[Objective]The objective of this study is to clone the small heat shock protein(sHSP)genes in Setosphaeria turcica,elucidate their structural characteristics,and explore their expression profiles during pathogen development and in response to HT-toxin induction.[Method]The hidden Markov model(HMM)was used to identify sHSP family members across the entire S.turcica genome.PCR technology was used to clone sHSP genes from S.turcica strain 01-23.Bioinformatics methods were then applied for the analysis of physicochemical properties,subcellular localization,structural prediction,and phylogenetic analysis of the sHSP genes obtained.Additionally,RNA-Seq and RT-qPCR were performed to determine the expression of sHSP genes across different developmental stages and during HT-toxin induction in S.turcica.[Result]Three sHSP family members(StHSP37.2,StHSP37.0 and StHSP22.6)were identified from the genome of S.turcica.The corresponding DNA sequences were successfully cloned from strain 01-23.The encoded sHSP proteins were weakly acidic and hydrophilic proteins,without transmembrane domain or signal peptide.Random coil in the secondary structure accounted for 58.97%to 60.35%,and β-turn ranged from 2.69%to 7.83%only.Subcellular localization prediction indicated that StHSP37.2 and StHSP37.0 were located in the nucleus,while StHSP22.6 was located in both nucleus and cytoplasm.Conserved ACD_sHSP-like domains were identified near C-terminus,with 2,3,and 5 conserved motifs in StHSP37.2,StHSP37.0,and StHSP22.6,respectively.The monomer tertiary structure models of sHSP were constructed using SWISS-Model and AlphaFill.Phylogenetic analysis indicated close relationships between StHSP22.6 and sHSP in Alternaria alternata,and between StHSP37.2/StHSP37.0 and sHSP in Bipolaris maydis.The sHSP genes of S.turcica had the highest expression levels in hyphae,followed by germ tubes,appressoria,and penetration pegs,with the lowest expression levels in conidia.StHSP22.6 and StHSP37.2 showed significant negative correlations with HT-toxin induction,and the relative gene expression was upregulated by 6.45 and 18.12 folds on day 14,respectively.On day 21 and 28,StHSP37.2 showed modest upregulations of 2.56 and 1.78 folds,respectively,while StHSP22.6 did not differ from the wild-type(WT).StHSP37.0 exhibited significant positive correlations with HT-toxin induction,with a significant downregulation by 59.23%,86.30%,and 88.11%on day 14,21,and 28,respectively.Exploration of expressed genes significantly associated with sHSP of S.turcica suggested that StHSP37.2 and StHSP22.6 were mainly related to HSP90,HSP104,catabolism,and mitochondrial Mg2+transport,while StHSP37.0 appeared to be associated with vacuolar alkaline amino acid transport,organic synthesis,and substance secretion.[Conclusion]The sHSP family members in S.turcica demonstrate a high degree of conservation yet exhibit structural and phylogenetic differences from other sHSPs.They are integral to the development of hyphae,germ tubes,appressoria,and penetration pegs,and also exert significant regulatory functions during HT-toxin induction.
张淑红;巩校东;张运峰;高凤菊;武秋颖;许可;李亚子;李艳梅;谷守芹;范永山
唐山师范学院生命科学系/河北省植物生物技术研究与应用重点实验室/唐山市农业病原真菌与毒素重点实验室,河北唐山 063000河北农业大学生命科学学院/河北省农业微生物生物信息利用技术创新中心,河北保定 071000
玉米大斑病菌小分子热激蛋白基因克隆结构分析HT-毒素诱导
Setosphaeria turcicasmall heat shock protein(sHSP)gene cloningstructure analysisHT-toxin induction
《中国农业科学》 2024 (017)
3384-3397 / 14
国家自然科学基金(22078171)、中央引导地方科技发展资金(236Z6508G)、河北省省级科技计划(21374301D)、唐山师范学院重点培育项目(ZDPY06,ZDPY08)
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