• 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AP2/ERF转录因子重鉴定及抗逆相关基因筛选

Re-identification of Tomato AP2/ERF Transcription Factors and Screening of Genes Related to Stress Resistance

  • 摘要:
    目的 本研究深入理解番茄AP2/ERF转录因子的组学特征及生物胁迫响应,促进其在番茄抗病育种中的应用。
    方法 利用最新公共数据进行AP2/ERF鉴定,结合番茄自交系在青枯菌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,主要分为两类;ERF亚家族包含93个(53.8%)成员,可进一步分为六类;DREB亚家族包含49个(28.3%)成员,可进一步分为两类;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,尤其是Solyc01g096860.3(AP2_2)与Solyc08g078190.2(ERF_5),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 To promote the germplasm application in tomato resistance breeding by gaining better insights on the genomic characteristics and biotic stress response of AP2/ERF transcription factors (TFs).
    Method AP2/ERF TFs were identified building on the recent release of genome data and genes related to bacterial wilt resistance were excavated, combined with the transcriptome sequencing of tomato inbred lines with Ralstonia solanacearum infection (RsI).
    Result A total of 173 AP2/ERF TFs were identified in tomato, which were mainly distributed in clusters at the ends of chromosomes, and 50.3% of them had collinearity, especially on chromosomes 3 and 8. Based on phylogenetic relationship, the AP2 subfamily contained 22 (12.7%) genes, which could be divided into two main categories; the ERF subfamily contained 93 (53.8%) genes and were further divided into six categories; the DREB subfamily contained 49 (28.3%) genes and were divided into two categories; and the RAV subfamily had only three genes. The Ka/Ks values of 71 pairs of tomato AP2/ERF homologs were all less than 1. 26.8% of AP2/ERF TFs were mainly expressed in roots, and the expression levels of genes in ERF_4-6 and DREB_2 categories were higher under several biotic stresses, especially Solyc03g005500.1 (ERF_6) and Solyc08g078170.1 (ERF_5). Ten differentially expressed AP2/ERF TFs (belonging to AP2 and ERF) were screened between resistant and susceptible tomato lines with RsI, of which Solyc06g068570.4 (AP2) was a positively regulated gene and the other nine were negatively regulated genes. 50.9% of tomato AP2/ERF TFs formed 193 pairs of interactions, of which the interaction between Solyc01g096860.3 (AP2_2) and Solyc08g078190.2 (ERF_5) was the most reliable, whereas the positive and negative interaction between Solyc06g068570.4 (AP2) and Solyc03g093560.1 (ERF_5) may play an important role in tomato response to bacterial wilt.
    Conclusion Tomato AP2/ERF TFs were comprehensively identified using genomic information and transcriptional expression, and several bacterial wilt response genes were obtained, which enriched the basic theory and genetic resources for tomato resistance breeding.

     

/

返回文章
返回