首页> 美国卫生研究院文献>Frontiers in Plant Science >Evaluation on the effectiveness of 2-deoxyglucose-6-phosphate phosphatase (DOGR1) gene as a selectable marker for oil palm (Elaeis guineensis Jacq.) embryogenic calli transformation mediated by Agrobacterium tumefaciens
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Evaluation on the effectiveness of 2-deoxyglucose-6-phosphate phosphatase (DOGR1) gene as a selectable marker for oil palm (Elaeis guineensis Jacq.) embryogenic calli transformation mediated by Agrobacterium tumefaciens

机译:评估农杆菌介导的2-脱氧葡萄糖-6-磷酸磷酸酶(DOGR1)基因作为油棕(Elaeis guineensis Jacq。)胚发生愈伤组织转化选择标记的有效性

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摘要

DOGR1, which encodes 2-deoxyglucose-6-phosphate phosphatase, has been used as a selectable marker gene to produce transgenic plants. In this study, a transformation vector, pBIDOG, which contains the DOGR1 gene, was transformed into oil palm embryogenic calli (EC) mediated by Agrobacterium tumefaciens strain LBA4404. Transformed EC were exposed to 400 mg l-1 2-deoxyglucose (2-DOG) as the selection agent. 2-DOG resistant tissues were regenerated into whole plantlets on various regeneration media containing the same concentration of 2-DOG. The plantlets were later transferred into soil and grown in a biosafety screenhouse. PCR and subsequently Southern blot analyses were carried out to confirm the integration of the transgene in the plantlets. A transformation efficiency of about 1.0% was obtained using DOGR1 gene into the genome of oil palm. This result demonstrates the potential of using combination of DOGR1 gene and 2-DOG for regenerating transgenic oil palm.
机译:编码2-脱氧葡萄糖-6磷酸磷酸酶的DOG R 1已被用作生产转基因植物的选择标记基因。在这项研究中,将包含DOG R 1基因的转化载体pBIDOG转化为根癌农杆菌LBA4404介导的油棕胚发生愈伤组织(EC)。将转化的EC暴露于400 mg l -1 2-脱氧葡萄糖(2-DOG)作为选择剂。 2-DOG抗性组织在含有相同浓度2-DOG的各种再生培养基上再生为整株苗。随后将小植株转移到土壤中,并在生物安全筛选室中生长。进行PCR和随后的Southern印迹分析以确认转基因在小植株中的整合。利用DOG R 1基因向油棕基因组转化的效率约为1.0%。该结果证明了使用DOG R 1基因和2-DOG的组合再生转基因油棕的潜力。

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