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乙型肝炎病毒DNA序列在人肝癌细胞系中的整合模式。

Integration pattern of hepatitis B virus DNA sequences in human hepatoma cell lines.

作者信息

Twist E M, Clark H F, Aden D P, Knowles B B, Plotkin S A

出版信息

J Virol. 1981 Jan;37(1):239-43. doi: 10.1128/JVI.37.1.239-243.1981.

Abstract

Four human hepatoma cell lines established from primary hepatocellular carcinomas were examined for the presence of hepatitis B virus DNA sequences. Reassociation kinetic analysis indicated that the cell lines HEp-3B 217, HEp-3B 14, HEp-3B F1, and PLC/PRF/5 contained two, one, one, and four genome equivalents per cell, respectively. Southern blot hybridization analysis demonstrated that hepatitis B virus DNA was integrated into the cellular DNAs of these cell lines. Further liquid hybridization studies with 32P-labeled HincII restriction fragments of hepatitis B virus DNA established that DNA sequences from all regions of the HBV genome were represented in the integrated viral sequences. Although the three HEp-3B cell lines were derived from the same tumor, they differed significantly in their patterns of integration of hepatitis B virus DNA, the number of copies of viral DNA per cell, and their ability to produce the virus-coded surface antigen.

摘要

对从原发性肝细胞癌建立的四个人肝癌细胞系进行了乙型肝炎病毒DNA序列检测。重缔合动力学分析表明,HEp-3B 217、HEp-3B 14、HEp-3B F1和PLC/PRF/5细胞系每个细胞分别含有两个、一个、一个和四个基因组当量。Southern印迹杂交分析表明,乙型肝炎病毒DNA已整合到这些细胞系的细胞DNA中。用32P标记的乙型肝炎病毒DNA的HincII限制性片段进行的进一步液相杂交研究证实,HBV基因组所有区域的DNA序列都存在于整合的病毒序列中。虽然三个HEp-3B细胞系来源于同一肿瘤,但它们在乙型肝炎病毒DNA的整合模式、每个细胞的病毒DNA拷贝数以及产生病毒编码表面抗原的能力方面存在显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c7a/171000/2d86470895a6/jvirol00001-0261-a.jpg

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