Christel Carl J, Schmied Patricia, Jagusch Verena, Schrödel Silke, Thirion Christian, Schmitt Kathrin, Salomon Michael
SIRION Biotech GmbH, Martinsried, Germany
SIRION Biotech GmbH, Martinsried, Germany.
J Biomol Screen. 2015 Sep;20(8):976-84. doi: 10.1177/1087057115581803. Epub 2015 Apr 14.
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.
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。