CAJ | 학술논문

目的制备含有增强型绿色荧光蛋白(enhanced green fluorescent protein,EGFP)报告基因的辛德毕斯病毒,并对其进行鉴定.方法采用融合PCR技术将报告基因EGFP融合到辛德毕斯病毒XJ-160感染性克隆pBR-XJ160的结构基因编码框后,并在报告基因前面添加亚基因启动子SP6,通过反向遗传学技术拯救得到EGFP标记的辛德毕斯病毒.结果成功拯救并获得了EGFP标记的XJ-160病毒,该重组病毒具有良好的荧光表达特性和遗传稳定性.结论 EGFP标记的辛德毕斯病毒可用于观测病毒的侵染轨迹,为进一步研究辛德毕斯病毒嗜性、生物学功能,以及感染机制奠定了基础.
목적 제비함유증강형록색형광단백(enhanced green fluorescent protein,EGFP)보고기인적신덕필사병독,병대기진행감정.방법 채용융합PCR기술장보고기인EGFP융합도신덕필사병독XJ-160감염성극륭pBR-XJ160적결구기인편마광후,병재보고기인전면첨가아기인계동자SP6,통과반향유전학기술증구득도EGFP표기적신덕필사병독.결과 성공증구병획득료EGFP표기적XJ-160병독,해중조병독구유량호적형광표체특성화유전은정성.결론 EGFP표기적신덕필사병독가용우관측병독적침염궤적,위진일보연구신덕필사병독기성、생물학공능,이급감염궤제전정료기출.
Objective To construct and characterize EGFP reporter gene labeled Sindbis virus (SINV).Methods The reporter gene EGFP was inserted into the genome of infectious clone pBR-XJ160 by using multi-fusion long fragment PCR method.Then apply reverse genetic manipulation technique to rescue and obtain EGFP labeled SINV.Results We successively obtained labeled SINV,which has good fluorescent expression characteristics and genetic stability.Conclusion The labeled virus can be seen in living cells and living body,and this serves as a good tool for cell and tissue tropism and biological function study of viruses.This study laid a foundation for further studying the cell tropism,biological functions and infection mechanism of SINV.