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纸质出版:2011
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郭艳,兰林,何长龙,洪国祜,程玲,毛青.基于pJFH-1的HCV全基因组扩增方法的建立[J].陆军军医大学学报(原第三军医大学学报),2011,33(11):1144-1147.
Guo Yan,Lan Lin,He Changlong,Hong Guohu,Cheng Ling,Mao Qing.Amplification of full-length hepatitis C virus genome based on plasmid pJFH-1[J].J Amry Med Univ (J Third Mil Med Univ),2011,33(11):1144-1147.
郭艳,兰林,何长龙,洪国祜,程玲,毛青.基于pJFH-1的HCV全基因组扩增方法的建立[J].陆军军医大学学报(原第三军医大学学报),2011,33(11):1144-1147. DOI:
Guo Yan,Lan Lin,He Changlong,Hong Guohu,Cheng Ling,Mao Qing.Amplification of full-length hepatitis C virus genome based on plasmid pJFH-1[J].J Amry Med Univ (J Third Mil Med Univ),2011,33(11):1144-1147. DOI:
目的 基于pJFH-1建立能稳定扩增HCV全基因组的长链PCR方法。 方法 以pJFH-1为测试模板,通过优化PCR扩增中各个重要环节,包括引物的选择、甘油和/或DMSO最适浓度的筛选、循环条件的摸索等,建立能稳定扩增HCV全基因组的长链PCR方案。 结果 高Tm值(>65 ℃)的引物更有利于HCV全基因组的扩增;5%、10%甘油或5% DMSO可显著提高PCR扩增的特异性和扩增效率,且甘油的促进作用优于DMSO;双温法较三温法能获得更高产量的PCR产物。 结论 通过优化长链PCR反应体系及条件,成功实现HCV基因全长的扩增。
Objective To optimize the protocols of long-PCR for amplifying full-length HCV genome based on plasmid pJFH-1. Methods Optimization of long-PCR strategies was performed by testing a series of primers
adding various concentrations of glycerol
DMSO or both
using different cycle systems to select the optimal long PCR conditions. Results Primers that have higher melting temperatures (65 ℃)could improve the efficiency of amplification. Glycerol of 5% and 10% or DMSO of 5% improved the specificity and efficiency of PCR amplification of full-length HCV genome. The promoting effect of glycerol was better than that of DMSO. Compared to three-stage temperature method
two-step temperature produced more PCR product. Conclusion Through the optimization of long-PCR protocol
full-length HCV genome is successfully achieved.
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