• 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

用于筛选后靶点验证和RNA干扰作用靶点控制的通用病毒载体策略

Versatile Viral Vector Strategies for Postscreening Target Validation and RNAi ON-Target Control.

作者信息

Christel Carl J, Schmied Patricia, Jagusch Verena, Schrödel Silke, Thirion Christian, Schmitt Kathrin, Salomon Michael

机构信息

SIRION Biotech GmbH, Martinsried, Germany

SIRION Biotech GmbH, Martinsried, Germany.

出版信息

J Biomol Screen. 2015 Sep;20(8):976-84. doi: 10.1177/1087057115581803. Epub 2015 Apr 14.

DOI:10.1177/1087057115581803
PMID:25873558
Abstract

Our approach aims to optimize postscreening target validation strategies using viral vector-driven RNA interference (RNAi) cell models. The RNAiONE validation platform is an array of plasmid-based expression vectors that each drives tandem expression of the gene of interest (GOI) with one small hairpin RNA (shRNA) from a set of computed candidate sequences. The best-performing shRNA (>85% silencing efficiency) is then integrated in an inducible, all-in-one lentiviral vector to transduce pharmacologically relevant cell types that endogenously express the GOI. VariCHECK is used subsequently to combine the inducible knockdown with an equally inducible rescue of the GOI for ON-target phenotype verification. The complete RNAiONE-VariCHECK system relies on three key elements to ensure high predictability: (1) maximized silencing efficiencies by a focused shRNA validation process, (2) homogeneity of the RNAi cell pools by application of sophisticated viral vector technologies, and (3) exploiting the advantages of inducible expression systems. By using a reversible expression system, our strategy adds critical information to hot candidates from RNAi screens and avoids potential side effects that may be caused by other, irreversible genomic manipulation methods such as transcription activator-like effector nucleases (TALEN) or clustered regularly interspaced short palindromic repeats/Cas9 (CRISPR/Cas). This approach will add credibility to top-hit screening candidates and protect researchers from costly misinterpretations early in the preclinical drug development process.

摘要

我们的方法旨在利用病毒载体驱动的RNA干扰(RNAi)细胞模型优化筛选后靶点验证策略。RNAiONE验证平台是一系列基于质粒的表达载体,每个载体驱动感兴趣基因(GOI)与一组通过计算得出的候选序列中的一个小发夹RNA(shRNA)串联表达。然后,将表现最佳的shRNA(沉默效率>85%)整合到一个可诱导的一体化慢病毒载体中,以转导内源性表达GOI的药理学相关细胞类型。随后使用VariCHECK将诱导型敲低与同样可诱导的GOI拯救相结合,用于验证靶标表型。完整的RNAiONE-VariCHECK系统依赖三个关键要素来确保高预测性:(1)通过聚焦的shRNA验证过程实现最大沉默效率;(2)应用先进的病毒载体技术使RNAi细胞池同质化;(3)利用诱导型表达系统的优势。通过使用可逆表达系统,我们的策略为RNAi筛选中的热门候选物增添了关键信息,并避免了其他不可逆基因组操作方法(如转录激活样效应核酸酶(TALEN)或成簇规律间隔短回文重复序列/Cas9(CRISPR/Cas))可能导致的潜在副作用。这种方法将为筛选出的顶级候选物增加可信度,并在临床前药物开发过程早期保护研究人员免受代价高昂的错误解读。

相似文献

1
Versatile Viral Vector Strategies for Postscreening Target Validation and RNAi ON-Target Control.用于筛选后靶点验证和RNA干扰作用靶点控制的通用病毒载体策略
J Biomol Screen. 2015 Sep;20(8):976-84. doi: 10.1177/1087057115581803. Epub 2015 Apr 14.
2
Short-term cytotoxic effects and long-term instability of RNAi delivered using lentiviral vectors.使用慢病毒载体递送RNAi的短期细胞毒性作用和长期不稳定性。
BMC Mol Biol. 2004 Aug 3;5:9. doi: 10.1186/1471-2199-5-9.
3
DNA vector-based RNA interference to study gene function in cancer.基于DNA载体的RNA干扰技术在癌症基因功能研究中的应用
J Vis Exp. 2012 Jun 4(64):e4129. doi: 10.3791/4129.
4
[The construction of lentivirus-mediated RNAi vector containing hTERT].[慢病毒介导的含人端粒酶逆转录酶的RNA干扰载体的构建]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):27-31.
5
Doxycycline-dependent inducible and reversible RNA interference mediated by a single lentivirus vector.由单一慢病毒载体介导的强力霉素依赖性诱导性和可逆性RNA干扰
Biosci Biotechnol Biochem. 2013;77(4):776-81. doi: 10.1271/bbb.120917. Epub 2013 Apr 7.
6
Conditional RNAi Using the Lentiviral GLTR System.使用慢病毒GLTR系统的条件性RNA干扰
Methods Mol Biol. 2016;1448:121-38. doi: 10.1007/978-1-4939-3753-0_10.
7
Viral vectors expressing a single microRNA-based short-hairpin RNA result in potent gene silencing in vitro and in vivo.表达单个基于 microRNA 的短发夹 RNA 的病毒载体在体外和体内导致有效的基因沉默。
J Biotechnol. 2014 Jan;169:71-81. doi: 10.1016/j.jbiotec.2013.11.004. Epub 2013 Nov 16.
8
CFTR inactivation by lentiviral vector-mediated RNA interference and CRISPR-Cas9 genome editing in human airway epithelial cells.慢病毒载体介导的RNA干扰和CRISPR-Cas9基因组编辑对人气道上皮细胞中CFTR的失活作用
Curr Gene Ther. 2015;15(5):447-59. doi: 10.2174/1566523215666150812115939.
9
Construction of simple and efficient DNA vector-based short hairpin RNA expression systems for specific gene silencing in mammalian cells.构建用于哺乳动物细胞中特定基因沉默的基于简单高效DNA载体的短发夹RNA表达系统。
Methods Mol Biol. 2007;408:223-41. doi: 10.1007/978-1-59745-547-3_13.
10
Gene down-regulation with short hairpin RNAs and validation of specificity by inducible rescue in mammalian cells.利用短发夹RNA进行基因下调以及通过哺乳动物细胞中的诱导性拯救验证特异性。
Curr Protoc Cell Biol. 2010 Dec;Chapter 27:Unit 27.2. doi: 10.1002/0471143030.cb2702s49.

引用本文的文献

1
Toward Tightly Tuned Gene Expression Following Lentiviral Vector Transduction.实现慢病毒载体转导后基因表达的紧密调控。
Viruses. 2020 Dec 11;12(12):1427. doi: 10.3390/v12121427.