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转座子介导的剪接突变细胞和小鼠模型的构建,以评估基于小核仁RNA的治疗方法的疗效。

Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based Therapeutics.

作者信息

Barbon Elena, Ferrarese Mattia, van Wittenberghe Laetitia, Sanatine Peggy, Ronzitti Giuseppe, Collaud Fanny, Colella Pasqualina, Pinotti Mirko, Mingozzi Federico

机构信息

Genethon, Evry, France.

INSERM U951, Evry, France.

出版信息

Mol Ther Nucleic Acids. 2016 Nov 29;5(11):e392. doi: 10.1038/mtna.2016.97.

Abstract

Disease-causing splicing mutations can be rescued by variants of the U1 small nuclear RNA (U1snRNAs). However, the evaluation of the efficacy and safety of modified U1snRNAs as therapeutic tools is limited by the availability of cellular and animal models specific for a given mutation. Hence, we exploited the hyperactive Sleeping Beauty transposon system (SB100X) to integrate human factor IX (hFIX) minigenes into genomic DNA in vitro and in vivo. We generated stable HEK293 cell lines and C57BL/6 mice harboring splicing-competent hFIX minigenes either wild type (SChFIX-wt) or mutated (SChFIXex5-2C). In both models the SChFIXex5-2C variant, found in patients affected by Hemophilia B, displayed an aberrant splicing pattern characterized by exon 5 skipping. This allowed us to test, for the first time in a genomic DNA context, the efficacy of the snRNA U1-fix9, delivered with an adeno-associated virus (AAV) vector. With this approach, we showed rescue of the correct splicing pattern of hFIX mRNA, leading to hFIX protein expression. These data validate the SB100X as a versatile tool to quickly generate models of human genetic mutations, to study their effect in a stable DNA context and to assess mutation-targeted therapeutic strategies.

摘要

致病剪接突变可通过U1小核RNA(U1snRNAs)的变体得到挽救。然而,作为治疗工具的修饰U1snRNAs的疗效和安全性评估受到特定突变的细胞和动物模型可用性的限制。因此,我们利用超活性睡美人转座子系统(SB100X)在体外和体内将人凝血因子IX(hFIX)小基因整合到基因组DNA中。我们生成了稳定的HEK293细胞系和C57BL/6小鼠,它们携带具有剪接能力的野生型(SChFIX-wt)或突变型(SChFIXex5-2C)hFIX小基因。在这两种模型中,在患有B型血友病的患者中发现的SChFIXex5-2C变体均表现出以第5外显子跳跃为特征的异常剪接模式。这使我们能够在基因组DNA背景下首次测试用腺相关病毒(AAV)载体递送的snRNA U1-fix9的疗效。通过这种方法,我们展示了hFIX mRNA正确剪接模式的挽救,导致hFIX蛋白表达。这些数据验证了SB100X作为一种通用工具,可快速生成人类基因突变模型,研究其在稳定DNA背景下的作用,并评估针对突变的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ee/5155329/43a276310008/mtna201697f1.jpg

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