• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

铁皮石斛LBD转录因子家族对瘤菌根菌侵染的表达响应及DoLOB1的分子特征分析

Response of LBD Transcription Factors to Epulorhiza Infection and Molecular Characterization of LOB1 in Dendrobium officinale

  • 摘要:
    目的 解析铁皮石斛LBD(LOB domain-containing)转录因子家族对瘤菌根菌共生的表达响应,并对其中显著响应的DoLOB1进行分子特征分析。
    方法 基于前期瘤菌根菌(Epulorhiza sp.)与铁皮石斛共生体系根系转录组数据,鉴定铁皮石斛LBD家族成员及其保守结构特征,并利用qRT-PCR分析接菌与未接菌根系中LBD家族成员的表达差异,对显著响应的DoLOB1基因进行克隆及功能相关特征分析。
    结果 基于转录组数据,从铁皮石斛根系中鉴定出23个LBD家族成员,其中20个属于Class I,3个成员属于Class II。qRT-PCR分析显示,接种瘤菌根菌(Epulorhiza sp.)后,LBD家族中11个基因显著差异表达。对显著响应的DoLOB1进一步分析发现,其开放阅读框长681 bp,编码226个氨基酸,预测蛋白分子量为24.7 kDa,理论等电点为6.21;原核表达获得约26 kDa的重组蛋白。系统进化分析表明,DoLOB1与单子叶植物LOB家族蛋白聚为一支,与美人蕉(Canna indica)亲缘关系最近,同源率为82.35%。亚细胞定位分析显示,DoLOB1-GFP融合蛋白荧光信号分布于细胞核、质膜和细胞质,具有明显的核定位特征。
    结论 铁皮石斛LBD家族多个成员对瘤菌根菌侵染表现出显著的表达响应,DoLOB1的结构和亚细胞定位特征,提示其可能参与铁皮石斛对菌根共生的响应。本研究为进一步解析LBD转录因子参与兰科植物菌根共生及根系发育的分子机制提供基础。

     

    Abstract:
    Objective Expression of LOB domain-containing transcription factors in response to Epulorhiza sp. inoculation and molecular characteristics of LOB1 in Dendrobium officinale were studied.
    Method Based on the previously obtained data on the root transcriptome in the symbiotic system of D. officinale and Epulorhiza sp., members and conserved structures of the LOB domain-containing (LBD) family were identified. Differential expressions of LBDs in the roots with and without Epulorhiza sp. infection were determined using qRT-PCR. Gene cloning, prokaryotic expression, phylogeny, and subcellular localization of the significantly responsive DoLOB1 was analyzed.
    Result Twenty-three LBDs were identified from the D. officinale root transcriptome that included 20 Class I members and 3 Class II DoLBD38, DoLBD39, and DoLBD40. They all contained the characteristic conserved LOB domain but were different in the compositions of GAS, leucine zipper-like, and other conserved motifs. The qRT-PCR analysis showed 11 of the 23 LBDs significantly differentially expressed by the Epulorhiza sp. inoculation. DoLOB1 had an ORF of 681 bp in length and encoded 226 amino acids with a molecular weight of 24.7 kDa and a theoretical isoelectric point of 6.21. The prokaryotic expression produced a recombinant protein of approximately 26 kDa. Phylogenetically, it clustered with LOBs of monocotyledonous plants and closely related with 82.35% sequence identity to Canna indica. Exhibiting a pronounced nuclear localization pattern, the DoLOB1-GFP fusion protein was distributed in the nucleus, plasma membrane, and cytoplasm.
    Conclusion Multiple DoLBDs showed significant expressions in response to Epulorhiza inoculation. Among them, DoLOB1 had the characteristic structural and subcellular localization features of LOB proteins and might participate in the mycorrhizal symbiosis of the medicinal plant.

     

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