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作 者:王勇[1] 王志中[1] 钟兵[1] 王恒[1] 邹庆华[1] 陈渝[2]
机构地区:[1]解放军第三军医大学西南医院风湿科研究所创伤,烧伤,复合伤国家重点实验室,重庆市400038 [2]解放军第三军医大学西南医院烧伤研究所创伤,烧伤,复合伤国家重点实验室,重庆市400038
出 处:《中国组织工程研究与临床康复》2011年第41期7719-7722,共4页Journal of Clinical Rehabilitative Tissue Engineering Research
基 金:the Natural Science Foundation of Chongqing Science and Technology Commission(General Program),No.2008BB5133;the National Natural Science Foundation of China,No.30973827~~
摘 要:背景:抗炎药物高通量筛选体系的建立,可为相关药物的研究提供一个理想的技术平台。目的:构建以核因子κB顺式作用元件4×CCL20基序为增强子,以SV40为启动子,以ZsGreen1-DR为报告基因的真核表达载体p4CCL20-ZsGreen1-DR。方法:以PGL2-control质粒为模板,PCR扩增目的片段SV40,两侧引入KpnⅠ/BamHⅠ酶切位点,克隆至pZsGreen1-DR质粒的Kpn Ⅰ/BamH Ⅰ酶切位点中,构建成pSV40-ZsGreen1-DR载体。将4×CCL20基序双链DNA克隆到pSV40-ZsGreen1-DR载体的BglⅡ和EcoRⅠ酶切位点之间,构建p4CCL20-ZsGreen1-DR重组质粒。结果与结论:经过DNA测序分析证实p4CCL20-ZsGreen1-DR重组质粒构建成功。该重组质粒可作为抗炎药物高通量筛选体系的基础。BACKGROUND:It is necessary to establish a high throughput screening system for anti-inflammatory drugs for rheumatoid arthritis.OBJECTIVE:To construct an eukaryotic expression vector p4CCL20-ZsGreen1-DR with the NF-?B cis-acting element 4×CCL20 motif as an enhancer,SV40 as a promoter,and ZsGreen1-DR as a reporter gene.METHODS:The target fragment SV40 was PCR amplified using PGL2-control plasmid as a template.KpnⅠ/Bam HⅠ restriction sites were introduced into the flank of the target fragment.Then,pSV40-ZsGreen1-DR vector was constructed by cloning the target fragment into pZsGreen1-DR plasmid.Finally,p4CCL20-ZsGreen1-DR plasmid was constructed by cloning the double strand DNA of 4×CCL20 motif(with BglⅡ and EcoRⅠ sticky ends at the 5' and 3' terminus,respectively) into the corresponding restriction sites of pSV40-ZsGreen1-DR vector(upstream of SV40 promoter).RESULTS AND CONCLUSION:DNA sequencing demonstrated successful construction of p4CCL20-ZsGreen1-DR plasmid.The construction of p4CCL20-ZsGreen1-DR plasmid might be useful to establish a high throughput screening system for anti-inflammatory drugs.
关 键 词:载体构建 CC亚族趋化因子配体20 不稳定型绿色荧光蛋白 测序分析
分 类 号:R318[医药卫生—生物医学工程]
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