首页> 美国卫生研究院文献>Journal of Virology >Expression Profiles of Bovine Adeno-Associated Virus and Avian Adeno-Associated Virus Display Significant Similarity to That of Adeno-Associated Virus Type 5
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Expression Profiles of Bovine Adeno-Associated Virus and Avian Adeno-Associated Virus Display Significant Similarity to That of Adeno-Associated Virus Type 5

机译:牛腺相关病毒和禽腺相关病毒的表达谱显示与5型腺相关病毒的表达显着相似。

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摘要

We present the first detailed expression profiles of nonprimate-derived adeno-associated viruses, namely, bovine adeno-associated virus (B-AAV) and avian adeno-associated virus (A-AAV), which were obtained after the infection of cell lines derived from their natural hosts. In general, the profiles of B-AAV and A-AAV were quite similar to that of AAV5; however, both exhibited features found for AAV2 as well. Like adeno-associated virus type 5 (AAV5), B-AAV and A-AAV utilized an internal polyadenylation site [(pA)p]; however, it was used to greater relative levels by B-AAV than by A-AAV. Similar to AAV5, >99% of B-AAV RNAs generated from upstream promoters were polyadenylated at (pA)p and hence not spliced. In contrast, ca. 50% of the A-AAV RNAs generated from upstream promoters read through (pA)p, as seen for AAV2. However, A-AAV generated lower levels of spliced P5 and P19 products than does AAV2, suggesting that A-AAV generates lower relative levels of Rep 68 and Rep 40. An additional difference in the expression profile of these viruses was that B-AAV generated a greater level of ITR-initiated RNAs than did A-AAV or AAV5. In addition, we demonstrate that, like AAV2, transactivation of transcription of the capsid-gene promoter of B-AAV required both adenovirus and targeting of its Rep protein to the transcription template; however, expression of the capsid-gene promoter of A-AAV was, like AAV5, largely independent of both adenovirus and its Rep proteins.
机译:我们介绍了非灵长类动物的腺相关病毒,即牛腺相关病毒(B-AAV)和禽腺相关病毒(A-AAV)的第一个详细的表达谱,它们是在感染细胞系后获得的从他们的自然宿主。通常,B-AAV和A-AAV的谱与AAV5的谱非常相似。但是,它们都具有针对AAV2的功能。像5型腺相关病毒(AAV5)一样,B-AAV和A-AAV也使用了内部聚腺苷酸化位点[(pA)p];但是,与A-AAV相比,B-AAV使用的相对水平更高。与AAV5相似,从上游启动子生成的B-AAV RNA中,有99%以上在(pA)p处被聚腺苷酸化,因此没有被剪接。相反,ca。如上游AAV2所见,由上游启动子产生的A-AAV RNA的50%会读通(pA)p。但是,与AAV2相比,A-AAV产生的剪接P5和P19产物水平较低,这表明A-AAV产生的Rep 68和Rep 40相对水平较低。这些病毒的表达谱的另一个差异是B-AAV产生ITR启动的RNA的水平比A-AAV或AAV5高。此外,我们证明,与AAV2一样,B-AAV衣壳基因启动子的转录反式激活既需要腺病毒,又需要将其Rep蛋白靶向转录模板。然而,A-AAV的衣壳基因启动子的表达与AAV5一样,很大程度上独立于腺病毒及其Rep蛋白。

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