高山离子芥冷诱导基因转化甘蔗二元植物表达载体构建
【目的】利用载体重组技术分别将高山离子芥冷诱导基因(Cbcor15a)和报告基因eGFP插入载体pCambia1300-bar,并引入玉米泛素基因启动子UBi-1代替载体本身启动子CaMV35s,重组为适合甘蔗转基因的二元植物表达载体pCambia1300-cbcor15a-bar。【方法】参照pCambia1300-bar载体多克隆位点和基因Cbcor15a、eGFP和启动子UBi-1的核苷酸序列设计引物,通过载体重组技术将基因和启动子分别插入相应的位点。利用基因枪分别将pCambia1300-bar载体和重组载体导入洋葱表皮细胞,用荧光显微镜和激光共聚焦显微镜观察。【结果】与导入pCamb...
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| Published in | 南方农业学报 Vol. 43; no. 9; pp. 1262 - 1268 |
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| Main Author | |
| Format | Journal Article |
| Language | Chinese |
| Published |
广西大学生命科学与技术学院,南宁530005
2012
广西作物遗传改良重点开放实验室,南宁530007%广西大学农学院,南宁,530005%广西甘蔗遗传改良重点实验室/广西农业科学院甘蔗研究所,南宁,530007%广西作物遗传改良重点开放实验室,南宁530007 广西甘蔗遗传改良重点实验室/广西农业科学院甘蔗研究所,南宁530007%亚热带农业生物资源保护利用重点实验室,南宁,530005 |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2095-1191 |
| DOI | 10.3969/j:issn.2095-1191.2012.09.1262 |
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| Summary: | 【目的】利用载体重组技术分别将高山离子芥冷诱导基因(Cbcor15a)和报告基因eGFP插入载体pCambia1300-bar,并引入玉米泛素基因启动子UBi-1代替载体本身启动子CaMV35s,重组为适合甘蔗转基因的二元植物表达载体pCambia1300-cbcor15a-bar。【方法】参照pCambia1300-bar载体多克隆位点和基因Cbcor15a、eGFP和启动子UBi-1的核苷酸序列设计引物,通过载体重组技术将基因和启动子分别插入相应的位点。利用基因枪分别将pCambia1300-bar载体和重组载体导入洋葱表皮细胞,用荧光显微镜和激光共聚焦显微镜观察。【结果】与导入pCambia1300-bar载体的洋葱表皮细胞相比较,导入重组载体pCambia1300-cbcor15a-bar的洋葱表皮细胞内有强烈的绿色荧光信号。【结论】重组甘蔗转基因二元植物表达载体启动子Ubi-1能够调控下游冷诱导基因Cbcor15a和报告基因eGFP的正常高效表达,为外源基因Cbcor15a转化甘蔗提供保障。 |
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| Bibliography: | 45-1381/S [Objective]A new bivalent plant expression vector,named pCambia1300-cbcor15a-bar,was recombined by inserting two genes,i.e.Cbcor15a and eGFP,into the vector pCambia1300-bar and replacing the promoter CaMV 35s with Ubi-1.[Method]Based on the multiple cloning sites of the expression vector pCambia1300-bar,the primers were designed according to the nucleotide sequence of gene Cbcor15a and eGFP and the promoter Ubi-1,and then the fragments of the genes and promoter were inserted into the vector pCambia1300-bar.The plasmids of the vector pCambia1300-cbcor15a-bar were transduced into onion epidermal cells via particle bombardment.The results were observed through fluorescence microscopy and confocal laser scanning microscope,respectively.[Result]Compared to onion epidermal cell with pCambia1300-bar,onion epidermal cell transduced with the recombinant vector plasmid had a very bright green florescence.[Conclusion]Downstream cold-induced gene Cbcor15a and reporter gene eGFP regulated by up-stream promoter Ub |
| ISSN: | 2095-1191 |
| DOI: | 10.3969/j:issn.2095-1191.2012.09.1262 |