Characterization of Zebrafish Polymerase III Promoters for the Expression of Short-Hairpin RNA Interference Molecules

被引:11
|
作者
Clarke, Brian D. [1 ,2 ]
Cummins, David M. [1 ]
McColl, Ken A. [1 ]
Ward, Alister C. [2 ]
Doran, Tim J. [1 ]
机构
[1] CSIRO Livestock Ind, Australian Anim Hlth Lab, Geelong, Vic 3220, Australia
[2] Deakin Univ, Mol Med Res Facil, Geelong, Vic 3217, Australia
关键词
DOUBLE-STRANDED-RNA; GENE KNOCKDOWN; SPH ELEMENT; U6; SIRNAS; TRANSCRIPTION; DEFECTS; DRIVEN; TRANSMISSION; INJECTION;
D O I
10.1089/zeb.2012.0782
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNA interference (RNAi) is a powerful, sequence specific, and long-lasting method of gene knockdown, and can be elicited by the expression of short-hairpin RNA (shRNA) molecules driven via polymerase III type 3 promoters from a DNA vector or transgene. To further develop RNAi as a tool in zebrafish, we have characterized the zebrafish U6 and H1 snRNA promoters and compared the efficiency of each of the promoters to express an shRNA and silence a reporter gene, relative to previously characterized U6 promoters from pufferfish, chicken, and mouse. Our results show that the zebrafish polymerase III promoters were capable of effective gene silencing in the zebrafish ZF4 cell line, but were ineffective in mammalian Vero cells. In contrast, mouse and chicken promoters were active in Vero but not ZF4 cells, highlighting the importance of homologous promoters to achieve effective silencing.
引用
收藏
页码:472 / 479
页数:8
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