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Integrated Hepatitis B Virus DNA Preserves the Binding Sequence of Transcription Factor Yin and Yang 1 at the Virus-Cell Junction

机译:整合的乙型肝炎病毒DNA在病毒-细胞交界处保留转录因子Yin和Yang 1的结合序列。

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摘要

Accumulated findings have indicated that hepatitis B virus (HBV) DNA integrates into the cellular DNA of HBV-infected chronic hepatitis tissues. The integrated sequence (IS) of HBV DNA at the virus-cell junction is conserved in a 25-bp region which is adjacent to direct repeat 1. A cellular protein which we purified from the nuclear extract of HepG2 cells binds to the IS and was designated IS binding protein 3 (ISBP3). The amino acid sequence of ISBP3 was determined and found to be identical to that of transcription initiation factor Yin and Yang 1 (YY1). An antibody against C-terminal amino acids of YY1 recognized ISBP3 in a Western blot analysis and an electrophoretic mobility shift assay. Furthermore, ISBP3 also interacted with Y3, which corresponds to the YY1 binding sequence, to enhance intramolecular recombination of polyomavirus DNA. Although YY1 is known as a transcription factor, the IS did not exhibit any effect on the transcription of precore and pregenome RNAs. The possible involvement of YY1 in the intramolecular recombination of linear replicative HBV DNA has been examined (Y. Hayashi et al., unpublished data). Data suggest that YY1 is involved in the joining reaction between HBV DNA and cellular DNA to form the virus-cell junction.
机译:累积的发现表明,乙型肝炎病毒(HBV)DNA整合入感染HBV的慢性肝炎组织的细胞DNA中。 HBV DNA在病毒-细胞连接处的整合序列(IS)保留在25 bp区域内,该区域与直接重复序列1相邻。我们从HepG2细胞的核提取物中纯化的细胞蛋白与IS结合,并且被称为IS结合蛋白3(ISBP3)。确定了ISBP3的氨基酸序列,发现其与转录起始因子Yin和Yang 1(YY1)的氨基酸序列相同。在Western印迹分析和电泳迁移率变动分析中,针对YY1的C末端氨基酸的抗体识别了ISBP3。此外,ISBP3还与对应于YY1结合序列的Y3相互作用,以增强多瘤病毒DNA的分子内重组。尽管YY1被称为转录因子,但IS对前核心和前基因组RNA的转录没有任何影响。已经检查了YY1可能参与线性复制HBV DNA的分子内重组(Y. Hayashi等人,未发表的数据)。数据表明,YY1参与了HBV DNA和细胞DNA之间的连接反应以形成病毒-细胞连接。

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