Detection of IFN Response of Non-Specific Effects on RNAi

Background and objective The RNA interference (RNAi) approach is an efficient and widely used method for silencing specific genes and exploring their functions. However, numerous studies have highlightedthe non-specific effects of RNAi experiments and the IFN response is one of the most common non-s...

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Published in:Chinese Journal of Lung Cancer
Main Authors: Yonggang LIANG, Hongyu LIU, Baoxing LIU, Yun BAI, Heng WU, Qinghua ZHOU, Jun CHEN
Format: Article
Language:Chinese
Published: Chinese Anti-Cancer Association; Chinese Antituberculosis Association 2009-01-01
Subjects:
Online Access:http://www.lungca.org/index.php?journal=01&page=article&op=view&path%5B%5D=10.3779%2Fj.issn.1009-3419.2009.01.017&path%5B%5D=195
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author Yonggang LIANG
Hongyu LIU
Baoxing LIU
Yun BAI
Heng WU
Qinghua ZHOU
Jun CHEN
author_facet Yonggang LIANG
Hongyu LIU
Baoxing LIU
Yun BAI
Heng WU
Qinghua ZHOU
Jun CHEN
author_sort Yonggang LIANG
collection DOAJ
container_title Chinese Journal of Lung Cancer
description Background and objective The RNA interference (RNAi) approach is an efficient and widely used method for silencing specific genes and exploring their functions. However, numerous studies have highlightedthe non-specific effects of RNAi experiments and the IFN response is one of the most common non-specific effects. In this research, we will study how to detect the IFN response in RNAi experiments. Methods Five different FLJ20420 siRNAs was transfected into human lung adenocarinoma cell line A549 using LipofectamineTM2000. The alternation of the interferon stimulated genes (ISGs) expression profile was analysed by real-time PCR and microarray assay. Results① Different FLJ20420 siRNA had different effect on silencing FLJ20420 mRNA expression in A549 cells, and FLJsiRNA-1 and -4 had the better effects to knockdown the expression of FLJ20420 (80% and 90% down-regulation, respectively); ② In analyzed 16 major ISGs, the expression of 14 of these genes was significantly increased in A549-FLJsiRNA-1 cells (P <0.05), while only 2 of these genes had a significant change in A549-FLJ-siRNA-4 cells. These results indicated an IFN response existed in A549-FLJ-siRNA-1 cells. ③ Microarray assay indicated that the expression of 51 ISGs were increased over 2 times in A549-FLJ-siRNA-1 cells, while only the expression of 6 ISGs were over 2-time in A549-FLJ-siRNA-4 cells. These results confirmed that there was an IFN response of non-specific effects of RNAi in A549 cells transfected with FLJ-siRNA-1. Conclusion In RNAi experiments, siRNA can not only silence the target genes, but also may activate IFN response. The analysis of the expression change of the major ISGs by real-time PCR is auseful approach to explore the IFN response in RNAi experiments.
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spelling doaj-art-3ffc9b1e82fe4591a565a5ab714a2abc2025-08-19T19:15:47ZzhoChinese Anti-Cancer Association; Chinese Antituberculosis AssociationChinese Journal of Lung Cancer1009-34191999-61872009-01-011211622Detection of IFN Response of Non-Specific Effects on RNAiYonggang LIANGHongyu LIUBaoxing LIUYun BAIHeng WUQinghua ZHOUJun CHENBackground and objective The RNA interference (RNAi) approach is an efficient and widely used method for silencing specific genes and exploring their functions. However, numerous studies have highlightedthe non-specific effects of RNAi experiments and the IFN response is one of the most common non-specific effects. In this research, we will study how to detect the IFN response in RNAi experiments. Methods Five different FLJ20420 siRNAs was transfected into human lung adenocarinoma cell line A549 using LipofectamineTM2000. The alternation of the interferon stimulated genes (ISGs) expression profile was analysed by real-time PCR and microarray assay. Results① Different FLJ20420 siRNA had different effect on silencing FLJ20420 mRNA expression in A549 cells, and FLJsiRNA-1 and -4 had the better effects to knockdown the expression of FLJ20420 (80% and 90% down-regulation, respectively); ② In analyzed 16 major ISGs, the expression of 14 of these genes was significantly increased in A549-FLJsiRNA-1 cells (P <0.05), while only 2 of these genes had a significant change in A549-FLJ-siRNA-4 cells. These results indicated an IFN response existed in A549-FLJ-siRNA-1 cells. ③ Microarray assay indicated that the expression of 51 ISGs were increased over 2 times in A549-FLJ-siRNA-1 cells, while only the expression of 6 ISGs were over 2-time in A549-FLJ-siRNA-4 cells. These results confirmed that there was an IFN response of non-specific effects of RNAi in A549 cells transfected with FLJ-siRNA-1. Conclusion In RNAi experiments, siRNA can not only silence the target genes, but also may activate IFN response. The analysis of the expression change of the major ISGs by real-time PCR is auseful approach to explore the IFN response in RNAi experiments.http://www.lungca.org/index.php?journal=01&page=article&op=view&path%5B%5D=10.3779%2Fj.issn.1009-3419.2009.01.017&path%5B%5D=195RNAiFLJ20420IFN responseISGs
spellingShingle Yonggang LIANG
Hongyu LIU
Baoxing LIU
Yun BAI
Heng WU
Qinghua ZHOU
Jun CHEN
Detection of IFN Response of Non-Specific Effects on RNAi
RNAi
FLJ20420
IFN response
ISGs
title Detection of IFN Response of Non-Specific Effects on RNAi
title_full Detection of IFN Response of Non-Specific Effects on RNAi
title_fullStr Detection of IFN Response of Non-Specific Effects on RNAi
title_full_unstemmed Detection of IFN Response of Non-Specific Effects on RNAi
title_short Detection of IFN Response of Non-Specific Effects on RNAi
title_sort detection of ifn response of non specific effects on rnai
topic RNAi
FLJ20420
IFN response
ISGs
url http://www.lungca.org/index.php?journal=01&page=article&op=view&path%5B%5D=10.3779%2Fj.issn.1009-3419.2009.01.017&path%5B%5D=195
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