Nakanishi-Matsui M, Hayashi Y, Kitamura Y, Koike K
Department of Gene Research, The Cancer Institute (JFCR), Toshima-ku, Tokyo 170-8455, Japan.
J Virol. 2000 Jun;74(12):5562-8. doi: 10.1128/jvi.74.12.5562-5568.2000.
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of YY1 in the intramolecular recombination of linear replicative HBV DNA has been examined (Y. Hayashi et al., unpublished data).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.
累积的研究结果表明,乙型肝炎病毒(HBV)DNA整合到HBV感染的慢性肝炎组织的细胞DNA中。病毒-细胞连接处HBV DNA的整合序列(IS)在与直接重复序列1相邻的一个25bp区域中是保守的。我们从HepG2细胞核提取物中纯化的一种细胞蛋白与该IS结合,并被命名为IS结合蛋白3(ISBP3)。测定了ISBP3的氨基酸序列,发现其与转录起始因子阴阳1(YY1)的氨基酸序列相同。在蛋白质免疫印迹分析和电泳迁移率变动分析中,针对YY1 C末端氨基酸的抗体识别出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是一种已知的转录因子,但该IS对前核心RNA和前基因组RNA的转录没有任何影响。已经研究了YY1可能参与线性复制型HBV DNA分子内重组的情况(Y. Hayashi等人,未发表数据)。数据表明,YY1参与了HBV DNA与细胞DNA之间的连接反应,以形成病毒-细胞连接处。