Sequence-non-specific effects generated by various types of RNA interference triggers

被引:15
作者
Olejniczak, Marta [1 ]
Urbanek, Martyna O. [1 ]
Jaworska, Edyta [1 ]
Witucki, Lukasz [1 ]
Szczesniak, Michal W. [2 ]
Makalowska, Izabela [2 ]
Krzyzosiak, Wlodzimierz J. [1 ]
机构
[1] Polish Acad Sci, Inst Bioorgan Chem, Dept Mol Biomed, Noskowskiego 12-14, PL-61704 Poznan, Poland
[2] Adam Mickiewicz Univ, Dept Bioinformat, Umultowska 89, PL-61614 Poznan, Poland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2016年 / 1859卷 / 02期
关键词
RNA interference; siRNA; Immune response; miRNA; Off-target; isomiRs; RNAimmuno; SHORT HAIRPIN RNAS; SIRNA; DNA; EXPRESSION; MICRORNAS; DELIVERY;
D O I
10.1016/j.bbagrm.2015.11.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA interference triggers such as short interfering RNA (siRNA) or genetically encoded short hairpin RNA (shRNA) and artificial miRNA (sh-miR) are widely used to silence the expression of specific genes. In addition to silencing selected targets, RNAi reagents may induce various side effects, including immune responses. To determine the molecular markers of immune response activation when using RNAi reagents, we analyzed the results of experiments gathered in the RNAimmuno (v 2.0) and GEO Profiles databases. To better characterize and compare cellular responses to various RNAi reagents in one experimental system, we designed a reagent series in corresponding siRNA, D-siRNA, 5hRNA and sh-miR forms. To exclude sequence-specific effects the reagents targeted 3 different transcripts (Luc, ATXN3 and HIT). We demonstrate that RNAi reagents induce a broad variety of sequence-non-specific effects, including the deregulation of cellular miRNA levels. Typical siRNAs are weak stimulators of interferon response but may saturate the miRNA biogenesis pathway, leading to the downregulation of highly expressed miRNAs, whereas plasmid-based reagents induce known markers of immune response and may alter miRNA levels and their isomiR composition. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:306 / 314
页数:9
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