Hüser Daniela, Weger Stefan, Heilbronn Regine
Department of Virology, Institute of Infectious Diseases, Free University of Berlin, Berlin, Germany.
J Virol. 2002 Aug;76(15):7554-9. doi: 10.1128/jvi.76.15.7554-7559.2002.
Adeno-associated virus type 2 (AAV-2) integrates specifically into a site on human chromosome 19 (chr-19) called AAVS1. To study the kinetics and frequency of chr-19-specific integration after AAV infection, we developed a rapid, sensitive, and quantitative real-time PCR assay for AAV inverted terminal repeat-chr-19-specific junctions. Despite the known variability of junction sites, conditions were established that ensured reliable quantification of integration rates within hours after AAV infection. The overall integration frequency was calculated to peak at between 10 and 20% of AAV-infected, unselected HeLa cells. At least 1 in 1,000 infectious AAV-2 particles was found to integrate site specifically up to day 4 postinfection in the absence of selection. Chromosomal breakpoints within AAVS1 agreed with those found in latently infected clonal cell lines and transgenic animals. Use of this quantitative real-time PCR will greatly facilitate the study of the early steps of wild-type and recombinant AAV vector integration.
2型腺相关病毒(AAV-2)特异性整合到人类19号染色体(chr-19)上一个名为AAVS1的位点。为了研究AAV感染后chr-19特异性整合的动力学和频率,我们开发了一种针对AAV反向末端重复序列-chr-19特异性连接的快速、灵敏且定量的实时PCR检测方法。尽管已知连接位点存在变异性,但我们建立了相关条件,确保在AAV感染后数小时内可靠地定量整合率。计算得出总体整合频率在未筛选的AAV感染的HeLa细胞中达到峰值,为10%至20%。在没有筛选的情况下,发现至少每1000个感染性AAV-2颗粒中有1个在感染后第4天特异性地整合到位点。AAVS1内的染色体断点与潜伏感染的克隆细胞系和转基因动物中的断点一致。这种定量实时PCR的应用将极大地促进对野生型和重组AAV载体整合早期步骤的研究。