一种基于RNA的转染试剂的合成、表征和功能。

Harsh V. Jain, Jessica F. Boehler, Kanneboyina Nagaraju, Serge L. Beaucage
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引用次数: 0

摘要

可以使用固相合成方案制备合成的8聚体、两亲性、反式作用的聚2'-O-甲基脲基硫代磷酸三酯RNA元件(2'-OMeUtaPS)。流式细胞术测量证明,2'-OMeUtaPS有效介导HeLa pLuc 705细胞中不带电的聚A尾磷酸二酰胺吗啉(PMO)序列的递送。在该细胞系中,2'-OMeUtaPS介导的反义polyA尾PMO序列的转染诱导异常萤光素酶前mRNA剪接位点的选择性剪接,导致功能性萤光素酶的恢复,如使用典型萤光素酶测定法定量测量的。2'-OMeUtaPS在肌营养不良的mdx小鼠模型的肌肉细胞中也能有效地递送不带电的反义polyA尾PMO序列;如琼脂糖凝胶电泳所示,针对编码突变的肌营养不良蛋白的前mRNA的剪接位点靶向polyA尾PMO序列触发交替剪接事件,该交替剪接事件导致从前mRNA切除突变的外显子(外显子23)并产生功能性肌营养不良素。©2018 John Wiley&Sons,股份有限公司版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthesis, Characterization, and Function of an RNA-Based Transfection Reagent

A synthetic 8-mer, amphipathic, trans-acting poly-2′-O-methyluridylic thiophosphate triester RNA element (2′-OMeUtaPS) can be prepared using solid-phase synthesis protocols. 2′-OMeUtaPS efficiently mediates the delivery of uncharged polyA-tailed phosphorodiamidate morpholino (PMO) sequences in HeLa pLuc 705 cells, as evidenced by flow cytometry measurements. In this cell line, 2′-OMeUtaPS-mediated transfection of an antisense polyA-tailed PMO sequence induces alternative splicing of an aberrant luciferase pre-mRNA splice site, leading to restoration of functional luciferase, as quantitatively measured using a typical luciferase assay. 2′-OMeUtaPS is also potent at delivering an uncharged antisense polyA-tailed PMO sequence in muscle cells of the mdx mouse model of muscular dystrophy; targeting the polyA-tailed PMO sequence against a splice site of the pre-mRNA encoding mutated dystrophin triggers an alternate splicing event that results in excision of the mutated exon (exon 23) from the pre-mRNA and production of functional dystrophin, as demonstrated by agarose gel electrophoresis. © 2018 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Nucleic Acid Chemistry
Current Protocols in Nucleic Acid Chemistry Chemistry-Organic Chemistry
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期刊介绍: Published in association with International Society for Nucleosides, Nucleotides & Nucleic Acids (IS3NA) , Current Protocols in Nucleic Acid Chemistry is equally valuable for biotech, pharmaceutical, and academic labs. It is the resource for designing and running successful research projects in the rapidly growing and changing field of nucleic acid, nucleotide, and nucleoside research.
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