• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

腺相关病毒进化过程中突变压力变化的历史:给基因治疗和 DNA 疫苗载体设计者的信息。

The history of mutational pressure changes during the evolution of adeno-associated viruses: A message to gene therapy and DNA-vaccine vectors designers.

机构信息

Department of General Chemistry, Belarusian State Medical University, Dzerzinskogo 83, Minsk, Belarus.

Biochemical Group of Multidisciplinary Diagnostic Laboratory, Institute of Physiology of the National Academy of Sciences of Belarus, Minsk, Belarus.

出版信息

Infect Genet Evol. 2020 Jan;77:104100. doi: 10.1016/j.meegid.2019.104100. Epub 2019 Oct 31.

DOI:10.1016/j.meegid.2019.104100
PMID:31678645
Abstract

The use of virus-associated vectors for gene therapy and vaccination have emerged as safe and effective delivery system. Like all other genetic materials, these vehicles are also prone to spontaneous mutations. To understand what types of nucleotide mutations are expected in the vector, one needs to know distinct characteristics of mutational process in the corresponding virus. In this study we analyzed mutational pressure directions along the length of the genomes of all types of primate adeno-associated viruses (AAV) that are frequently used in gene therapy or DNA-vaccines. We observed clear evidences of transcription-associated mutational pressure in AAV: nucleotide usage biases are changing drastically after each of the three promoters: the higher the rate of transcription, the stronger the bias towards GC to AT mutations. Moreover, the usage of G decreased at the lower transcription rate (after P19 promoter) than the usage of C (after P40 promoter). Since nucleotide usage biases are retrospective indices, we created a scenario of changes in transcriptional map during the AAV evolution. Current mutational pressure directions are different for AAV types, while all of them demonstrate high rates of T to C transitions in the second long ORF. Since transcription rate and cell tropism are the main factors determining the preferable direction of nucleotide mutations in AAV, mutational pressure should be checked experimentally in DNA vectors before their final design with the aim to make the transferred gene more stable against those mutations.

摘要

病毒相关载体在基因治疗和疫苗接种中的应用已成为安全有效的递送系统。与所有其他遗传物质一样,这些载体也容易发生自发突变。为了了解载体中预期会出现哪些类型的核苷酸突变,需要了解相应病毒中突变过程的独特特征。在这项研究中,我们分析了在基因治疗或 DNA 疫苗中经常使用的所有类型灵长类腺相关病毒(AAV)基因组长度上的突变压力方向。我们观察到 AAV 中转录相关突变压力的明显证据:在三个启动子中的每一个之后,核苷酸使用偏倚都会发生剧烈变化:转录率越高,GC 向 AT 突变的偏倚越强。此外,在较低转录率(在 P19 启动子之后)下 G 的使用减少,低于 C 的使用(在 P40 启动子之后)。由于核苷酸使用偏倚是回顾性指标,我们在 AAV 进化过程中创建了转录图谱变化的情景。目前的突变压力方向因 AAV 类型而异,而所有类型在第二个长 ORF 中均显示出 T 到 C 转换的高速率。由于转录率和细胞嗜性是决定 AAV 中核苷酸突变首选方向的主要因素,因此在最终设计 DNA 载体之前,应在实验中检查突变压力,以使转移基因对这些突变更稳定。

相似文献

1
The history of mutational pressure changes during the evolution of adeno-associated viruses: A message to gene therapy and DNA-vaccine vectors designers.腺相关病毒进化过程中突变压力变化的历史:给基因治疗和 DNA 疫苗载体设计者的信息。
Infect Genet Evol. 2020 Jan;77:104100. doi: 10.1016/j.meegid.2019.104100. Epub 2019 Oct 31.
2
Mutational analysis of the adeno-associated virus type 2 (AAV2) capsid gene and construction of AAV2 vectors with altered tropism.2型腺相关病毒(AAV2)衣壳基因的突变分析及嗜性改变的AAV2载体构建
J Virol. 2000 Sep;74(18):8635-47. doi: 10.1128/jvi.74.18.8635-8647.2000.
3
Chromosomal latency and expression at map unit 96 of a wild-type plus adeno-associated virus (AAV)/Neo vector and identification of p81, a new AAV transcriptional promoter.野生型腺相关病毒(AAV)/Neo载体在96图距单位处的染色体潜伏与表达以及新型AAV转录启动子p81的鉴定。
J Hum Virol. 1999 Nov-Dec;2(6):359-68.
4
Novel caprine adeno-associated virus (AAV) capsid (AAV-Go.1) is closely related to the primate AAV-5 and has unique tropism and neutralization properties.新型山羊腺相关病毒(AAV)衣壳(AAV-Go.1)与灵长类动物AAV-5密切相关,并具有独特的嗜性和中和特性。
J Virol. 2005 Dec;79(24):15238-45. doi: 10.1128/JVI.79.24.15238-15245.2005.
5
The Adeno-associated Virus - A Safe and Promising Vehicle for Liverspecific Gene Therapy of Inherited and Non-inherited Disorders.腺相关病毒——用于遗传性和非遗传性疾病肝脏特异性基因治疗的安全且有前景的载体。
Curr Gene Ther. 2017;17(1):4-16. doi: 10.2174/1566523217666170314141931.
6
Expression of the human multidrug resistance and glucocerebrosidase cDNAs from adeno-associated vectors: efficient promoter activity of AAV sequences and in vivo delivery via liposomes.腺相关载体表达人多药耐药和葡萄糖脑苷脂酶cDNA:腺相关病毒序列的高效启动子活性及通过脂质体进行体内递送
Hum Gene Ther. 1996 Jul 10;7(11):1309-22. doi: 10.1089/hum.1996.7.11-1309.
7
A Regulatory Element Near the 3' End of the Adeno-Associated Virus rep Gene Inhibits Adenovirus Replication in cis by Means of p40 Promoter-Associated Short Transcripts.腺相关病毒rep基因3'端附近的一个调控元件通过与p40启动子相关的短转录本顺式抑制腺病毒复制。
J Virol. 2016 Mar 28;90(8):3981-93. doi: 10.1128/JVI.03120-15. Print 2016 Apr.
8
Expressing Transgenes That Exceed the Packaging Capacity of Adeno-Associated Virus Capsids.表达超过腺相关病毒衣壳包装能力的转基因。
Hum Gene Ther Methods. 2016 Feb;27(1):1-12. doi: 10.1089/hgtb.2015.140.
9
Designer gene delivery vectors: molecular engineering and evolution of adeno-associated viral vectors for enhanced gene transfer.定制基因递送载体:腺相关病毒载体的分子工程改造与进化以增强基因转移
Pharm Res. 2008 Mar;25(3):489-99. doi: 10.1007/s11095-007-9431-0. Epub 2007 Sep 1.
10
Generation of Targeted Adeno-Associated Virus (AAV) Vectors for Human Gene Therapy.用于人类基因治疗的靶向腺相关病毒(AAV)载体的生成
Curr Pharm Des. 2015;21(22):3248-56. doi: 10.2174/1381612821666150531171653.

引用本文的文献

1
Translation-Associated Mutational U-Pressure in the First ORF of SARS-CoV-2 and Other Coronaviruses.SARS-CoV-2及其他冠状病毒首个开放阅读框中的翻译相关突变U压力
Front Microbiol. 2020 Sep 22;11:559165. doi: 10.3389/fmicb.2020.559165. eCollection 2020.