Linden R M, Winocour E, Berns K I
Department of Microbiology, Hearst Microbiology Research Center, Cornell University Medical College, NY 10021, USA.
Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7966-72. doi: 10.1073/pnas.93.15.7966.
The adeno-associated virus (AAV) genome integrates site specifically into a defined region of human chromosome 19 (termed AAVS1). Using a functional assay for AAV integration into AAVS1 DNA propagated as an episome, we obtained evidence that a 33-nucleotide AAVS1 DNA sequence contains the minimum signal required for targeted integration. The recombination signal comprises a DNA-binding motif for the AAV regulatory Rep protein [Rep binding site (RBS)] separated by an eight-nucleotide spacer from a sequence that can act as a substrate for Rep endonucleolytic activity [terminal resolution site (TRS)]. Mutations in either the AAVS1-encoded RBS or TRS elements abort targeted integration. Since both the RBS and TRS elements are present in the viral origin of replication and are required for AAV replication, targeted integration into chromosome 19 AAVS1 DNA may involve a replicative type of recombination that is discussed. An additional chromosome 19 element, which is responsible for DNA rearrangements in episomes propagating AAVS1 DNA, was identified and shown not to be required for AAV episomal integration, despite its location adjacent to the recombination signal.
腺相关病毒(AAV)基因组可特异性地整合到人类19号染色体的一个特定区域(称为AAVS1)。通过对AAV整合到作为附加体进行增殖的AAVS1 DNA的功能检测,我们获得了证据,表明一段33个核苷酸的AAVS1 DNA序列包含靶向整合所需的最小信号。该重组信号包括一个用于AAV调节性Rep蛋白的DNA结合基序[Rep结合位点(RBS)],它与一个可作为Rep内切核酸酶活性底物的序列[末端分辨率位点(TRS)]被一个8个核苷酸的间隔区隔开。AAVS1编码的RBS或TRS元件中的突变会导致靶向整合失败。由于RBS和TRS元件都存在于病毒复制起点中,并且是AAV复制所必需的,因此靶向整合到19号染色体AAVS1 DNA中可能涉及一种文中所讨论的复制型重组。另外还鉴定出了一个19号染色体元件,它负责在传播AAVS1 DNA的附加体中发生DNA重排,并且尽管其位于重组信号附近,但已证明它对于AAV附加体整合并非必需。