Suppr超能文献

2型腺相关病毒载体的高效复制:末端重复序列之外的顺式作用元件及最小尺寸

Efficient replication of adeno-associated virus type 2 vectors: a cis-acting element outside of the terminal repeats and a minimal size.

作者信息

Tullis G E, Shenk T

机构信息

Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544-1014, USA.

出版信息

J Virol. 2000 Dec;74(24):11511-21. doi: 10.1128/jvi.74.24.11511-11521.2000.

Abstract

Recombinant adeno-associated virus type 2 (AAV2) can be produced in adenovirus-infected cells by cotransfecting a plasmid containing the recombinant AAV2 genome, which is generally comprised of the viral terminal repeats flanking a transgene, together with a second plasmid expressing the AAV2 rep and cap genes. However, recombinant viruses generally replicate inefficiently, often producing 100-fold fewer virus particles per cell than can be obtained after transfection with a plasmid containing a wild-type AAV2 genome. We demonstrate that this defect is due, at least in part, to the presence of a positive-acting cis element between nucleotides 194 and 1882 of AAV2. Recombinant AAV2 genomes lacking this region accumulated 14-fold less double-stranded, monomer-length replicative-form DNA than did wild-type AAV2. In addition, we demonstrate that a minimum genome size of 3.5 kb is required for efficient production of single-stranded viral DNA. Relatively small recombinant genomes (2,992 and 3,445 bp) accumulated three- to eightfold less single-stranded DNA per monomer-length replicative-form DNA molecule than wild-type AAV2. In contrast, recombinant AAV2 with larger genomes (3,555 to 4,712 bp) accumulated similar amounts of single-stranded DNA per monomer-length replicative-form DNA compared to wild-type AAV2. Analysis of two recombinant AAV2 genomes less than 3.5 kb in size indicated that they were deficient in the production of the extended form of monomer-length replicative-form DNA, which is thought to be the immediate precursor to single-stranded AAV2 DNA.

摘要

重组腺相关病毒2型(AAV2)可通过共转染包含重组AAV2基因组的质粒在腺病毒感染的细胞中产生,该基因组通常由侧翼为转基因的病毒末端重复序列组成,同时转染表达AAV2 rep和cap基因的第二个质粒。然而,重组病毒通常复制效率低下,每个细胞产生的病毒颗粒通常比用包含野生型AAV2基因组的质粒转染后获得的病毒颗粒少100倍。我们证明,这种缺陷至少部分是由于AAV2核苷酸194至1882之间存在一个正向作用的顺式元件。缺乏该区域的重组AAV2基因组积累的双链单体长度复制形式DNA比野生型AAV2少14倍。此外,我们证明,有效产生单链病毒DNA需要最小基因组大小为3.5 kb。相对较小的重组基因组(2992和3445 bp)每个单体长度复制形式DNA分子积累的单链DNA比野生型AAV2少三至八倍。相比之下,基因组较大(3555至4712 bp)的重组AAV2与野生型AAV2相比,每个单体长度复制形式DNA积累的单链DNA量相似。对两个大小小于3.5 kb的重组AAV2基因组的分析表明,它们在产生单体长度复制形式DNA的延伸形式方面存在缺陷,而这种延伸形式被认为是单链AAV2 DNA的直接前体。

相似文献

引用本文的文献

1
Construction of an rAAV Producer Cell Line through Synthetic Biology.通过合成生物学构建 rAAV 生产细胞系。
ACS Synth Biol. 2022 Oct 21;11(10):3285-3295. doi: 10.1021/acssynbio.2c00207. Epub 2022 Oct 11.

本文引用的文献

6
cis requirements for the efficient production of recombinant DNA vectors based on autonomous parvoviruses.
Hum Gene Ther. 1999 Jul 1;10(10):1619-32. doi: 10.1089/10430349950017626.
7
Optimization of packaging of adeno-associated virus gene therapy vectors using plasmid transfections.
J Virol Methods. 1998 Dec;76(1-2):31-41. doi: 10.1016/s0166-0934(98)00120-7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验