Sui J M, Li G, Chen G X, Yu M Y, Ding S T, Wang J S, Qiao L X
College of Life Science, Qingdao Agricultural University, Key Laboratory of Qingdao Major Crop Germplasm Resource Innovation and Application, Key Lab of Plant Biotechnology in Universities of Shandong, Qingdao, Shandong, China.
College of Foreign Languages, Qingdao Agricultural University, Qingdao, Shandong, China.
Genet Mol Res. 2017 Mar 8;16(1):gmr-16-01-gmr.16019432. doi: 10.4238/gmr16019432.
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.
Rab蛋白家族是小GTP结合蛋白中最大的家族。其中,已知RabG基因对非生物胁迫有响应,但植物中RabG基因介导的胁迫响应分子机制尚不清楚。为了研究花生中AhRabG基因的分子机制,获得了过表达AhRabG基因(S6)的转基因植株,其耐盐性相对高于非转基因植株(S7)。对盐胁迫处理前后S6和S7植株的叶片进行了数字基因表达(DGE)测序。发现花生中的AhRabG基因参与了“光合作用”、“氧化磷酸化”、“AMPK信号通路”、“植物激素信号转导”等一些途径。基于S6和S7植株的比较,在五个采样时间点共发现298个差异表达基因(DEG)上调或下调。其中,132个DEG在盐胁迫处理后对S6和/或S7中的盐胁迫有响应。这132个DEG包括编码各种转录因子的基因以及参与耐盐胁迫的蛋白质,如MYB、AP2、RING-H2锌指蛋白、晚期胚胎丰富(LEA)蛋白、脱水响应蛋白RD22、过氧化物酶、CBL相互作用蛋白激酶、钙结合蛋白等。本研究的信息将有助于进一步研究阐明RabG基因赋予花生耐盐性的机制。