Dutheil Nathalie, Henckaerts Els, Kohlbrenner Erik, Linden R Michael
Department of Infectious Diseases, King's College London School of Medicine, London SE1 9RT, United Kingdom.
J Virol. 2009 Dec;83(23):12512-25. doi: 10.1128/JVI.01754-09. Epub 2009 Sep 16.
The nonpathogenic human adeno-associated virus type 2 (AAV-2) has adopted a unique mechanism to site-specifically integrate its genome into the human MBS85 gene, which is embedded in AAVS1 on chromosome 19. The fact that AAV has evolved to integrate into this ubiquitously transcribed region and that the chromosomal motifs required for integration are located a few nucleotides upstream of the translation initiation start codon of MBS85 suggests that the transcriptional activity of MBS85 might influence site-specific integration and thus might be involved in the evolution of this mechanism. In order to begin addressing this question, we initiated the characterization of the human MBS85 promoter region and compared its transcriptional activity to that of the AAV-2 p5 promoter. Our results clearly indicate that AAVS1 is defined by a complex transcriptional environment and that the MBS85 promoter shares key regulatory elements with the viral p5 promoter. Furthermore, we provide evidence for bidirectional MBS85 promoter activity and demonstrate that the minimal motifs required for AAV site-specific integration are present in the 5' untranslated region of the gene and play a posttranscriptional role in the regulation of MBS85 expression. These findings should provide a framework to further elucidate the complex interactions between the virus and its cellular host in this unique pathway to latency.
非致病性人类2型腺相关病毒(AAV-2)采用了一种独特机制,将其基因组位点特异性整合到人类MBS85基因中,该基因位于19号染色体上的AAVS1区域。AAV进化到整合到这个普遍转录的区域,且整合所需的染色体基序位于MBS85翻译起始密码子上游几个核苷酸处,这一事实表明MBS85的转录活性可能影响位点特异性整合,因此可能参与了这一机制的进化。为了开始解决这个问题,我们着手对人类MBS85启动子区域进行表征,并将其转录活性与AAV-2 p5启动子的转录活性进行比较。我们的结果清楚地表明,AAVS1由复杂的转录环境定义,并且MBS85启动子与病毒p5启动子共享关键调控元件。此外,我们提供了MBS85启动子双向活性的证据,并证明AAV位点特异性整合所需的最小基序存在于该基因的5'非翻译区,并在MBS85表达调控中发挥转录后作用。这些发现应为进一步阐明病毒与其细胞宿主在这一独特潜伏途径中的复杂相互作用提供一个框架。