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首页> 外文期刊>Journal of genetics >In planta transformation of sorghum (Sorghum bicolor (L.) Moench) using TPS1 gene for enhancing tolerance to abiotic stresses
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In planta transformation of sorghum (Sorghum bicolor (L.) Moench) using TPS1 gene for enhancing tolerance to abiotic stresses

机译:使用TPS1基因增强对非生物胁迫的耐受性在高粱(高粱)中进行植物转化

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An in planta transformation protocol for sorghum (Sorghum bicolor (L.) Moench) using shoot apical meristem of germinating seedlings is reported in this study. Agrobacterium tumefaciens strain, LBA4404 with pCAMBIA1303 vector and construct pCAMBIA1303TPS1 were individually used for transformation. Since, the transgene is integrated into the cells of already differentiated tissues, the T-0 plants were chimeric and stable integration was observed in T-1 generation. -Glucuronidase (GUS) expression in the seedlings and spikelets of emerging cob was the first indication of transformability in T-0 generation which was further confirmed by PCR analysis using hpt and TPS1 gene-specific primers. Screening on 25 mg/L hygromycin combined with PCR analysis was used for selection of transformants in the T-1 generation. Transformation efficiencies ranged between 34-38% and 26-34% using pCAMBIA1303 vector and construct pCAMBIA1303TPS1, respectively. Molecular characterization of the T-2 transgenics using PCR, RT-PCR and Southern blot analyses further revealed the integration, expression and inheritance of the transgene. These results indicate the feasibility of the method to generate transgenics with pCAMBIA1303 vector and construct pCAMBIA1303TPS1. The abiotic stress tolerance of TPS1 transgenics developed in the present study was evident by the ability of the transformants to tolerate 200 mM NaCl as well as higher root growth and biomass.
机译:在这项研究中报道了使用发芽幼苗的茎尖分生组织对高粱(高粱)进行植物内转化的方案。带有pCAMBIA1303载体的根癌农杆菌菌株LBA4404和构建体pCAMBIA1303TPS1分别用于转化。由于转基因已整合到已经分化的组织的细胞中,因此T-0植物是嵌合的,并且在T-1世代中观察到了稳定的整合。 -葡糖醛酸糖苷酶(GUS)在萌芽穗轴的幼苗和小穗中的表达是T-0代可转化性的第一个指示,这通过使用hpt和TPS1基因特异性引物的PCR分析进一步证实。 25 mg / L潮霉素的筛选与PCR分析相结合,用于选择T-1代中的转化子。使用pCAMBIA1303载体和构建pCAMBIA1303TPS1的转化效率分别在34-38%和26-34%之间。使用PCR,RT-PCR和Southern印迹分析对T-2转基因进行分子鉴定,进一步揭示了转基因的整合,表达和遗传。这些结果表明了用pCAMBIA1303载体产生转基因并构建pCAMBIA1303TPS1的方法的可行性。本研究中开发的TPS1转基因生物的非生物胁迫耐受性通过转化体耐受200 mM NaCl以及更高的根系生长和生物量的能力得到了证明。

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