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Digital expression analysis of the genes associated with salinity resistance after overexpression of a stress-responsive small GTP-binding RabG protein in peanut

机译:花生中胁迫响应小GTP结合RabG蛋白过表达后与耐盐性相关基因的数字表达分析

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The Rab protein family is the largest family of the small GTP-binding proteins. Among them, the RabG genes are known to be responsive to abiotic stresses, but the molecular mechanisms of the stress responses mediated by RabG genes in plants is poorly understood. To investigate the molecular mechanism of AhRabG gene in peanut, transgenic plants overexpressing the AhRabG gene (S6) with relatively higher salinity resistance than the non-transgenic plants (S7) were obtained. Digital gene expression (DGE) sequencing was performed with the leaves of S6 and S7 plants before and after salinity-stress treatment. The AhRabG gene in peanut was found to be involved in a few pathways such as “photosynthesis”, “oxidative phosphorylation”, “AMPK signaling pathway”, “plant hormone signal transduction”, etc. A total of 298 differentially expressed genes (DEGs) were found to be upregulated or downregulated at five sampling time points based on the comparison between S6 and S7 plants. Among them, 132 DEGs were responsive to salinity stress in S6 and/or S7 after salinity-stress treatment. These 132 DEGs included genes encoding various transcription factors and proteins involved in resistance to salinity stress such as MYB, AP2, RING-H2 zinc finger proteins, late embryogenesis abundant (LEA) proteins, dehydration-responsive protein RD22, peroxidases, CBL-interacting protein kinases, calcium-binding proteins, and others. The information from this study will be useful for further studies on elucidating the mechanism of salinity resistance conferred by RabG genein peanut.
机译:Rab蛋白家族是小GTP结合蛋白的最大家族。其中,已知RabG基因对非生物胁迫有反应,但是对植物中由RabG基因介导的胁迫反应的分子机制了解甚少。为了研究花生中的AhRabG基因的分子机制,获得了过表达AhRabG基因的转基因植物(S6),其耐盐性比非转基因植物(S7)高。在盐胁迫处理之前和之后,对S6和S7植物的叶片进行数字基因表达(DGE)测序。发现花生中的AhRabG基因参与了一些途径,例如“光合作用”,“氧化磷酸化”,“ AMPK信号传导途径”,“植物激素信号传导”等。共有298个差异表达基因(DEG)根据S6和S7植物之间的比较,发现在五个采样时间点上调或下调浓度。其中,在盐胁迫处理后,S6和/或S7中的132个DEG对盐胁迫响应。这132个DEG包括编码各种转录因子的基因和与盐分抗性有关的蛋白质,例如MYB,AP2,RING-H2锌指蛋白,晚期胚胎生成(LEA)蛋白,脱水反应蛋白RD22,过氧化物酶,CBL相互作用蛋白激酶,钙结合蛋白等。这项研究提供的信息将有助于进一步研究阐明RabG基因在花生中赋予耐盐性的机制。

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