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作 者:陈健[1] 刘启福[1] 魏琦[1] 吴祥褆 王宇[1]
机构地区:[1]广西肿瘤防治研究所,广西医学院,北京医科大学人民医院肝病研究所
出 处:《生物化学杂志》1994年第5期611-615,共5页
摘 要:采用核酸分子杂交Southern印迹法,以32P标记的HBVDNA为探针,检测HBsAg阳性母亲引产的40例胎儿的肝、肾组织。结果有2例胎肝和1例胎肾细胞DNA出现大于3.2kb的杂交带,表明HBVDNA已处于整合状态。胎肾细胞基因组中查出HBVDNA整合为首次报道。This paper reports the detection results of HBV DNA sequences state in liver and kidney cell genomes of fetuses aborted from HBsAg positive mothers by Southern blot hybridization technique and cloned HBV DNA as probe labelled with 32P. In 40 fetuses,specific hybridization bands corresponding to high molecular weight DNA over 3. 2 kb of HBV DNA were observed in cellular DNAs extracted from 2 cases of fetal liver and I case of fetal kidney tissues after digestion by EcoRI and hybridization with 32P HBV DNA probe. The results showed that HBV DNA sequences could integrate into hepatocyte and kidney cell genomes. The integration of HBV DNA in cell genomes might occur randomly since the integrating bands in fetal celluar DNA did not appear at same position. HBV DNA sequence was not found in the remaining tissue samples. None of free HBV DNA hybridization band could be detected in the cellular DNAs extracted from all fetal organs studied.
分 类 号:R512.620.2[医药卫生—内科学]
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