摘要
目的克隆并表达HDAg基因,确定HDAg蛋白在细胞内定位。方法常规分子克隆、错配PCR、Western blot、RT-PCR及免疫细胞化学等。结果通过RT-PCR及错配PCR方法从1例HBV/HDV重叠感染患者血清中成功克隆出HDAg基因,生物信息学分析证实其来源于我国流行的基因I型河南株。将HDAg基因克隆于真核载体转染肝细胞,证实两种不同形式的HDAg主要定位在细胞核。结论 HDAg定位于细胞核可能是其发挥相应生物学作用的基础。
Objective To identify the cellular localization of HDAg protein after the cloning and expression of HDAg gene. Methods Routine molecular cloning, mismatch amplification mutation assay, Western blot, RT-PCR and immu nofluorescenee assay were adopted. Results In this study, HDAg gene was cloned from a patient' s serum co-infected with HBV/HDV. The analysis of bioinformaties supported the evidence of genotype I from Henan strain. The entire cod ing sequence of HDAg was cloned into an eukaryotic vector. The expression vector was transfected into human liver HepG2 cells. Expression products of both L-HDAg and S-HDAg were observed to loealizate in the nuclei by immunofluo rescence assay. Conclusion HDAg may play an important role through its cell localization in the nucleus.
出处
《胃肠病学和肝病学杂志》
CAS
2013年第6期538-541,共4页
Chinese Journal of Gastroenterology and Hepatology
基金
国家自然科学基金(30972594)
王宝恩肝纤维化基金(2010-14)