• 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

番茄APETALA2乙烯响应因子重鉴定及抗逆相关基因筛选

Re-identification of AP2/ERF Transcription Factors in Search for Disease Resistance-related Genes in Tomato Plant

  • 摘要:
    目的 探明番茄APETALA2乙烯响应因子(APETALA2/ethylene-responsive factor, AP2/ERF)的组学特征及生物胁迫响应机制,促进其在番茄抗病育种中的应用。
    方法 利用新版公共数据进行AP2/ERF鉴定,结合番茄自交系在青枯菌(Ralstonia solanacearum)侵染下的转录测序数据,挖掘青枯病抗性相关AP2/ERF。
    结果 173个番茄AP2/ERF转录因子家族成员被鉴定,主要成簇分布在染色体端部,50.3%的AP2/ERF具有共线性,尤其是3号和8号染色体。基于系统进化关系,AP2亚家族包含22个(12.7%)成员,主要分为2类;ERF亚家族包含93个(53.8%)成员,可进一步分为6类;DREB亚家族包含49个(28.3%)成员,可进一步分为2类;RAV亚家族仅有3个成员。71对AP2/ERF同源基因的Ka/Ks值均小于1。26.8%的AP2/ERF主要在根中表达,几种生物胁迫下,ERF_4-6和DREB_2基因转录表达水平较高,尤其是Solyc03g005500.1(ERF_6)和Solyc08g078170.1(ERF_5)。青枯菌侵染下,在抗、感材料间筛选到10个差异表达AP2/ERF(分属AP2和ERF),其中Solyc06g068570.4(AP2)为正调控基因,其他9个为负调控基因。50.9%的AP2/ERF形成193对互作关系,Solyc01g096860.3(AP2_2)与Solyc08g078190.2(ERF_5)互作可信度最大,而Solyc06g068570.4(AP2)与Solyc03g093560.1(ERF_5)正负互作在番茄青枯病响应中可能发挥重要作用。
    结论 综合基因组分析和转录表达鉴定了番茄AP2/ERF转录因子,获得若干青枯病响应基因,丰富了番茄抗病育种基础理论和基因资源。

     

    Abstract:
    Objective Genomics and stress response of tomato AP2/ERF transcription factors (TFs) were studied for breeding applications.
    Method Based on the recently available genetic information related to bacterial wilt resistance, tomato AP2/ERF TFs were reexamined for confirmation. Using the transcriptome sequence of tomato inbred lines infected by Ralstonia solanacearum (Rs), the re-identified TFs were analyzed to search for genes related to disease-resistance.
    Result One-hundred-seventy-three AP2/ERF TFs were identified from the data bank. They were mainly in the clusters at the ends of chromosomes, especially Chromosomes 3 and 8, with 50.3% of them collinearity. Phylogenetically, the AP2 subfamily had 22 genes (i.e., 12.7% of total) in two main categories; the ERF subfamily, 93 genes (i.e., 53.8% of total) in 6 categories; the DREB subfamily, 49 genes (i.e., 28.3% of total) in two categories; and the RAV subfamily, 3 genes. The Ka/Ks of the 71 pairs of tomato AP2/ERF homologs were all lower than 1. Of the AP2/ERF TFs, 26.8% were expressed largely in the roots and more highly under certain biotic stresses in the ERF_4-6 and DREB_2 categories, especially Solyc03g005500.1 (ERF_6) and Solyc08g078170.1 (ERF_5). Ten AP2/ERF TFs, belonging separately to AP2 and ERF, differentially expressed in the Rs-resistant and Rs-susceptible tomato lines. Among them, Solyc06g068570.4 (AP2) was positively regulated, and the remainders negatively regulated. The other 50.9% of the AP2/ERF TFs became 193 interacting pairs, of which the one between Solyc01g096860.3 (AP2_2) and Solyc08g078190.2 (ERF_5) was most reliable. The positive and negative interactions between Solyc06g068570.4 (AP2) and Solyc03g093560.1 (ERF_5) might also involve in the response of a tomato plant to the bacterial wilt.
    Conclusion The AP2/ERF TFs associated with the response of a tomato plant to bacterial wilt were confirmed using the newly available information on the genome and transcriptome. By studying the differential genes in the Rs-resistant and Rs-susceptible inbred tomato lines, specific genes were identified for further studies and breeding applications.

     

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