Effects of Self-Complementarity, Codon Optimization, Transgene, and Dose on Liver Transduction with AAV8.

Q1 Immunology and Microbiology Human Gene Therapy Methods Pub Date : 2016-12-01 DOI:10.1089/HGTB.2016.039
Peter Bell, Lili Wang, Shu-Jen Chen, Hongwei Yu, Yanqing Zhu, Mohamad Nayal, Zhenning He, J. White, Deborah Lebel-Hagan, James M. Wilson
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引用次数: 17

Abstract

Numerous methods of vector design and delivery have been employed in an attempt to increase transgene expression following AAV-based gene therapy. Here, a gene transfer study was conducted in mice to compare the effects of vector self-complementarity (double- or single-stranded DNA), codon optimization of the transgene, and vector dose on transgene expression levels in the liver. Two different reporter genes were used: human ornithine transcarbamylase (hOTC) detected by immunofluorescence, and enhanced green fluorescent protein (EGFP) detected by direct fluorescence. The AAV8 capsid was chosen for all experiments due to its strong liver tropism. While EGFP is already a codon-optimized version of the original gene, both wild-type (WT) and codon-optimized (co) versions of the hOTC transgene were compared in this study. In addition, the study evaluated which of the two hOTC modifications-codon optimization or self-complementarity-would confer the highest increase in expression levels at a given dose. Interestingly, based on morphometric image analysis, it was observed that the difference in detectable expression levels between self-complementary (sc) and single-stranded (ss) hOTCco vectors was dose dependent, with a sevenfold increase in OTC-positive area using sc vectors at a dose of 3 × 109 genome copies (GC) per mouse, but no significant difference at a dose of 1 × 1010 GC/mouse. In contrast, with EGFP as a transgene, the increases in expression levels when using the sc vector were observed at both the 3 × 109 GC/mouse and 1 × 1010 GC/mouse doses. Furthermore, codon optimization of the hOTC transgene generated a more significant improvement in expression than the use of self-complementarity did. Overall, the results demonstrate that increases in expression levels gained by using sc vectors instead of ss vectors can vary between different transgenes, and that codon optimization of the transgene can have an even more powerful effect on the resulting expression levels.
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自互补、密码子优化、转基因和剂量对AAV8肝转导的影响。
在以aav为基础的基因治疗后,已经采用了许多载体设计和递送方法来增加转基因表达。本研究在小鼠中进行了一项基因转移研究,比较了载体自互补(双链或单链DNA)、转基因密码子优化和载体剂量对肝脏中转基因表达水平的影响。采用两种不同的报告基因:免疫荧光法检测人鸟氨酸转氨基甲酰基酶(hOTC),直接荧光法检测增强型绿色荧光蛋白(EGFP)。所有实验均选用AAV8衣壳,因为其具有较强的肝向性。虽然EGFP已经是原始基因的密码子优化版本,但本研究比较了野生型(WT)和密码子优化(co)版本的hOTC转基因。此外,该研究评估了两种hOTC修饰——密码子优化或自互补——在给定剂量下,哪一种修饰会使表达水平增加最多。有趣的是,基于形态图像分析,观察到自互补(sc)和单链(ss) hOTCco载体之间可检测表达水平的差异是剂量依赖性的,在每只小鼠3 × 109个基因组拷贝(GC)剂量下,sc载体的otc阳性面积增加了7倍,但在1 × 1010个GC/小鼠剂量下无显著差异。相比之下,EGFP作为转基因,当使用sc载体时,在3 × 109 GC/小鼠和1 × 1010 GC/小鼠剂量下均观察到表达水平的增加。此外,hOTC转基因的密码子优化比使用自互补产生更显著的表达改善。总的来说,结果表明,使用sc载体而不是ss载体获得的表达水平的增加在不同的转基因之间是不同的,并且转基因的密码子优化可以对最终的表达水平产生更强大的影响。
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来源期刊
Human Gene Therapy Methods
Human Gene Therapy Methods BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Human Gene Therapy is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes in-depth coverage of DNA, RNA, and cell therapies by delivering the latest breakthroughs in research and technologies. Human Gene Therapy provides a central forum for scientific and clinical information, including ethical, legal, regulatory, social, and commercial issues, which enables the advancement and progress of therapeutic procedures leading to improved patient outcomes, and ultimately, to curing diseases. The Journal is divided into three parts. Human Gene Therapy, the flagship, is published 12 times per year. HGT Methods, a bimonthly journal, focuses on the applications of gene therapy to product testing and development. HGT Clinical Development, a quarterly journal, serves as a venue for publishing data relevant to the regulatory review and commercial development of cell and gene therapy products.
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