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Packaging of Human Chromosome 19-Specific Adeno-Associated Virus (AAV) Integration Sites in AAV Virions during AAV Wild-Type and Recombinant AAV Vector Production

机译:在AAV野生型和重组AAV载体生产过程中,在AAV病毒颗粒中包装人染色体19特异性腺相关病毒(AAV)整合位点

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摘要

Adeno-associated virus type 2 (AAV-2) establishes latency by site-specific integration into a unique locus on human chromosome 19, called AAVS1. During the development of a sensitive real-time PCR assay for site-specific integration, AAV-AAVS1 junctions were reproducibly detected in highly purified AAV wild-type and recombinant AAV vector stocks. A series of controls documented that the junctions were packaged in AAV capsids and were newly generated during a single round of AAV production. Cloned junctions displayed variable AAV sequences fused to AAVS1. These data suggest that packaged junctions represent footprints of AAV integration during productive infection. Apparently, AAV latency established by site-specific integration and the helper virus-dependent, productive AAV cycle are more closely related than previously thought.
机译:腺相关病毒2型(AAV-2)通过将位点特异性整合到人类19号染色体上称为AAVS1的独特基因座中来建立潜伏期。在开发针对位点特异性整合的实时荧光定量PCR检测方法的过程中,在高纯度AAV野生型和重组AAV载体中可重复检测AAV-AAVS1连接。一系列控制记录表明,这些连接处被包装在AAV衣壳中,是在单轮AAV生产中新产生的。克隆的接头显示了与AAVS1融合的可变AAV序列。这些数据表明,包装的路口代表了生产性感染期间AAV整合的足迹。显然,通过特定于站点的整合和依赖辅助病毒的生产性AAV周期建立的A​​AV潜伏期比以前认为的更为紧密。

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