大鼠免疫球蛋白样转录物3过表达腺病毒载体的构建及鉴定
投稿时间:2016-01-23  修订日期:2016-01-27  点此下载全文
引用本文:周恒,唐其柱,邓伟,袁园,倪健,靳亚阁.大鼠免疫球蛋白样转录物3过表达腺病毒载体的构建及鉴定[J].医学研究杂志,2016,45(8):24-28
DOI: 10.11969/j.issn.1673-548X.2016.08.008
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作者单位E-mail
周恒 430060 武汉大学人民医院心内科、武汉大学心血管病研究所  
唐其柱 430060 武汉大学人民医院心内科、武汉大学心血管病研究所 qztang@whu.edu.cn 
邓伟 430060 武汉大学人民医院心内科、武汉大学心血管病研究所  
袁园 430060 武汉大学人民医院心内科、武汉大学心血管病研究所  
倪健 430060 武汉大学人民医院心内科、武汉大学心血管病研究所  
靳亚阁 430060 武汉大学人民医院心内科、武汉大学心血管病研究所  
基金项目:国家自然科学基金资助项目(81300070,81270303,81470516,81530012);教育部高等学校博士学科点专项科研基金资助项目(20130141130010)
中文摘要:目的 构建免疫球蛋白样转录物3(immunoglobulin-like transcript 3,ILT3)过表达腺病毒载体,以期进一步研究ILT3基因功能及其在心血管疾病中的作用。方法 针对大鼠ILT3设计引物,通过PCR扩增获取目的基因,以琼脂糖凝胶电泳鉴定,行胶回收与PCR产物纯化。使用限制性内切酶BamHⅠ与AgeⅠ对载体质粒以及纯化后的PCR产物进行双酶切,将酶切后的PCR产物与载体连接,连接产物加入至感受态细胞培养后挑取菌落进行PCR鉴定、测序、比对及质粒抽提。将ILT3重组质粒与腺病毒辅助包装质粒共转染至 HEK293细胞,获取病毒粗提液并进行扩增、纯化,终点稀释法进行病毒效价检测,在荧光显微镜下观察腺病毒转染效率。结果 PCR与测序鉴定表明GV314-ILT3重组质粒构建成功。终点稀释法测得病毒效价为1×109 PFU/ml,荧光显微镜下观察显示病毒转染效率较高。结论 携带ILT3基因的腺病毒载体构建成功,获取的腺病毒具有较高的效价与转染效率。
中文关键词:免疫球蛋白样转录物3  质粒  腺病毒  过表达  基因重组
 
Construction and Identification of Recombinant Adenovirus Vector which Overexpresses Rat Immunoglobulin-like Transcript 3
Abstract:Objective To construct recombinant adenovirus vector which overexpresses immunoglobulin-like transcript 3 (ILT3) in order to further study the function of ILT3 and its effect in cardiovascular diseases. Methods The primers of rat ILT3 were designed, and the target gene were amplified by PCR and identified by agarose gel electrophoresis. The gel was recovered and PCR products were purified. Digested plasmid vector and PCR products using restriction endonuclease BamHI and ageI were connected and added to competent cells, and the cultured colonies were identified by PCR and sequencing. ILT3 recombinant plasmid and adenovirus packaging plasmid were co-transfected into HEK293 cells, and the obtained adenovirus were amplified and purified. Virus titer were detected using the endpoint dilution assay, and the transfection efficiency was observed under the fluorescence microscope. Results PCR and sequencing analysis showed that the recombinant plasmid of GV314-ILT3 was successfully constructed. The virus titer was 1×109 PFU/ml and the transfection efficiency was high under fluorescence microscope. Conclusion The adenovirus vector which overexpresses ILT3 was constructed successfully, and the obtained adenovirus exhibited high titer and transfection efficiency.
keywords:Immunoglobulin-like transcript 3  Plasmid  Adenovirus  Overexpression  Gene recombination
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