Inhibition of porcine endogenous retrovirus in PK15 cell line by efficient multitargeting RNA interference

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Title
Inhibition of porcine endogenous retrovirus in PK15 cell line by efficient multitargeting RNA interference
Author(s)
H C Chung; V G Nguyen; H J Moon; Hye Kwon Kim; Seong-Jun Park; J H Lee; M G Choi; A R Kim; B K Park
Bibliographic Citation
Transplant International, vol. 27, no. 1, pp. 96-105
Publication Year
2014
Abstract
To effectively suppress porcine endogenous retroviruses (PERV)s, RNAi technique was utilized. RNAi is the up-to-date skill for gene knockdown which simultaneously multitargets both gag and pol genes critical for replication of PERVs. Previously, two of the most effective siRNAs (gag2, pol2) were found to reduce the expression of PERVs. Concurrent treatment of these two siRNAs (gag2+pol2) showed knockdown efficiency of up to 88% compared to negative control. However, despite the high initial knockdown efficiency 48 h after transfection caused by siRNA, it may only be a transient effect of suppressing PERVs. The multitargeting vector was designed, containing both gag and pol genes and making use of POL II miR Expression Vector, which allowed for persistent and multiple targeting. This is the latest shRNA system technique expressing and targeting like miRNA. Through antibiotics resistance characteristics utilizing this vector, miRNA-transfected PK15 cells (gag2-pol2) were selected during 10 days. An 88.1% reduction in the level of mRNA expression was found. In addition, we performed RT-activity analysis and fluorescence in situ hybridization assay, and it demonstrated the highest knockdown efficiency in multitargeting (gag2+pol2) miRNA group. Therefore, according to the results above, gene knockdown system (siRNA and shRNA) through multitargeting strategy could effectively inhibit PERVs.
Keyword
inhibitionmultitargetingPK15 cellsporcine endogenous retrovirusRNA interference
ISSN
0934-0874
Publisher
Wiley
DOI
http://dx.doi.org/10.1111/tri.12219
Type
Article
Appears in Collections:
1. Journal Articles > Journal Articles
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