Zhou Dinggang, Wang Chunfeng, Li Zhu, Chen Yun, Gao Shiwu, Guo Jinlong, Lu Wenying, Su Yachun, Xu Liping, Que Youxiong
Key Laboratory of Sugarcane Biology and Genetic Breeding, Fujian Agriculture and Forestry University, Ministry of Agriculture Fuzhou, China.
Front Plant Sci. 2016 Mar 8;7:279. doi: 10.3389/fpls.2016.00279. eCollection 2016.
Genetic engineering offers an attractive alternative in sugarcane breeding for increasing cane and sugar yields as well as disease and insect resistance. Bar transgenic sugarcane employing the herbicide tolerance is a useful agronomical trait in weed control. In this study, a loop-mediated isothermal amplification (LAMP) assay for rapid detection of the bar gene in transgenic sugarcane has been developed and evaluated. A set of six primers was designed for LAMP-based amplification of the bar gene. The LAMP reaction conditions were optimized as follows: 5.25 mM of Mg(2+), 6:1 ratio of inner vs. outer primer, and 6.0 U of Bst DNA polymerase in a reaction volume of 25.0 μL. The detection limit of the recombinant plasmid 1Ac0229 was as low as 10 copies in the developed LAMP, which was 10-fold higher sensitive than that of conventional PCR. In 100 putative transgenic lines, the bar gene was detected in 100/100 cases (100%) by LAMP and 97/100 cases (97%) by conventional PCR, respectively. In conclusion, the developed LAMP assay is visual, rapid, sensitive, reliable, and cost-effective for detection of the bar specific transgenic sugarcane.
基因工程为甘蔗育种提供了一个有吸引力的选择,可提高甘蔗产量和糖分产量以及抗病虫能力。采用除草剂耐受性的转bar基因甘蔗在杂草控制方面是一种有用的农艺性状。在本研究中,已开发并评估了一种用于快速检测转基因甘蔗中bar基因的环介导等温扩增(LAMP)检测方法。设计了一组六条引物用于基于LAMP的bar基因扩增。LAMP反应条件优化如下:在25.0 μL反应体积中,Mg(2+)浓度为5.25 mM,内引物与外引物比例为6:1,Bst DNA聚合酶用量为6.0 U。在开发的LAMP检测中,重组质粒1Ac0229的检测限低至10个拷贝,比传统PCR灵敏度高10倍。在100个推定的转基因株系中,通过LAMP分别在100/100例(100%)中检测到bar基因,通过传统PCR在97/100例(97%)中检测到bar基因。总之,所开发的LAMP检测方法在检测bar特异性转基因甘蔗时具有可视化、快速、灵敏、可靠且经济高效的特点。