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腺相关病毒的位点特异性整合由细胞DNA序列指导。

Site-specific integration by adeno-associated virus is directed by a cellular DNA sequence.

作者信息

Giraud C, Winocour E, Berns K I

机构信息

Department of Microbiology, Hearst Microbiology Research Center, Cornell University Medical College, New York, NY 10021.

出版信息

Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):10039-43. doi: 10.1073/pnas.91.21.10039.

Abstract

Different regions of an 8.2-kb cloned DNA segment containing the target for adeno-associated virus (AAV) integration in human chromosome 19q13-3-qter (AAVS1 locus) were subcloned in an Epstein-Barr virus-based shuttle vector and propagated as episomes in a derivative of the 293 human embryonic kidney cell line. Preferential recombination with an infecting AAV genome was assessed by measuring the frequency of recombinants among the shuttle vectors recovered in Escherichia coli. The signals which direct recombination with the AAV genome were localized to a 510-nt region at the 5' end of the 8.2-kb AAVS1 DNA. Hence, the results indicate that site-specific integration of AAV is directed by a specific DNA sequence on human chromosome 19. An unusual degree of DNA heterogeneity in the recovered vector was also associated with the 510 nt at the 5' end of AAVS1 DNA, suggesting that the AAV chromosomal integration locus may be involved in genomic instability.

摘要

包含腺相关病毒(AAV)整合靶点的一个8.2kb克隆DNA片段的不同区域,该靶点位于人类19号染色体q13-3至qter(AAVS1位点),被亚克隆到基于爱泼斯坦-巴尔病毒的穿梭载体中,并在293人胚肾细胞系的一个衍生物中作为附加体进行增殖。通过测量在大肠杆菌中回收的穿梭载体中重组体的频率,评估与感染性AAV基因组的优先重组。与AAV基因组指导重组的信号定位于8.2kb AAVS1 DNA 5'端的一个510nt区域。因此,结果表明AAV的位点特异性整合由人类19号染色体上的一个特定DNA序列指导。回收载体中不同寻常程度的DNA异质性也与AAVS1 DNA 5'端的510nt相关,这表明AAV染色体整合位点可能与基因组不稳定性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5944/44953/142618e80c93/pnas01143-0385-a.jpg

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