Yellisetty Varalaxmi, Reddy L A, Mandapaka Maheswari
Division of Crop Sciences, Central Research Institute for Dryland Agriculture, Santhoshnagar, Hyderabad 500 059, India.
J Genet. 2015 Sep;94(3):425-34. doi: 10.1007/s12041-015-0540-y.
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 T1 generation. β-Glucuronidase (GUS) expression in the seedlings and spikelets of emerging cob was the first indication of transformability in T0 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 T1 generation. Transformation efficiencies ranged between 34-38% and 26-34% using pCAMBIA1303 vector and construct pCAMBIA1303TPS1, respectively. Molecular characterization of the T2 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 pCAM-BIA1303 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.
本研究报道了一种利用发芽幼苗的茎尖分生组织对高粱(Sorghum bicolor (L.) Moench)进行植株内转化的方法。分别使用携带pCAMBIA1303载体的根癌农杆菌菌株LBA4404和构建体pCAMBIA1303TPS1进行转化。由于转基因整合到已经分化组织的细胞中,T0代植株是嵌合体,在T1代观察到稳定整合。β-葡萄糖醛酸酶(GUS)在幼苗和新出现的雌穗小穗中的表达是T0代可转化性的第一个指标,这通过使用hpt和TPS1基因特异性引物的PCR分析进一步得到证实。在25 mg/L潮霉素上进行筛选并结合PCR分析用于T1代转化体的选择。使用pCAMBIA1303载体和构建体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T2代转基因植株进行分子表征,进一步揭示了转基因的整合、表达和遗传。这些结果表明用pCAM - BIA1303载体和构建体pCAMBIA1303TPS1产生转基因植株的方法是可行的。本研究中培育的TPS1转基因植株对非生物胁迫的耐受性通过转化体能耐受200 mM NaCl以及更高的根生长和生物量得以体现。