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
相关论文
共 50 条
  • [31] The cytomegalovirus promoter-driven short hairpin RNA constructs mediate effective RNA interference in zebrafish in vivo
    Su, Jianguo
    Zhu, Zuoyan
    Wang, Yaping
    Xiong, Feng
    Zou, Jun
    MARINE BIOTECHNOLOGY, 2008, 10 (03) : 262 - 269
  • [32] Construction and Assessment of Short-Hairpin RNA Eukaryotic Expression Vector Targeting TGF-β1 Labeled by GFP
    Li, Na
    Han, Yaling
    Qi, Yanmei
    Guo, Liang
    Yan, Chenhui
    CIRCULATION, 2010, 122 (02) : E94 - E94
  • [33] Adenovirus expression of short hairpin RNA: The road to vector-mediated in vivo RNA interference
    Cautlon, JD
    Clay, CM
    MOLECULAR THERAPY, 2003, 7 (05) : S305 - S305
  • [34] Expression Arrest™ short hairpin RNA libraries:: solutions for transient, stable and in vivo RNA interference
    Fewell, G
    JOURNAL OF NEUROCHEMISTRY, 2005, 94 : 15 - 15
  • [35] Characterization and comparison of chicken U6 promoters for the expression of short hairpin RNAs
    Wise, Terry G.
    Schafer, Darren J.
    Lambeth, Luke S.
    Tyack, Scott G.
    Bruce, Matthew P.
    Moore, Robert J.
    Doran, Tim J.
    ANIMAL BIOTECHNOLOGY, 2007, 18 (03) : 153 - 162
  • [36] Attenuation of SARS coronavirus by a short hairpin RNA expression plasmid targeting RNA-dependent RNA polymerase
    Lu, AL
    Zhang, HQ
    Zhang, XY
    Wang, HX
    Hu, QK
    Shen, L
    Schaffhausen, BS
    Hou, WM
    Li, LS
    VIROLOGY, 2004, 324 (01) : 84 - 89
  • [37] Zebrafish U6 promoter driving short-hairpin RNA expression for PmRab7 knockdown to inhibit yellow head virus infection in shrimp hemocytes
    Thaiprasansup, Wilasinee
    Pewkliang, Yongyut
    Hoa Khanh Tran Kiem
    Nuntakarn, Lalana
    Taengchaiyaphum, Suparat
    Saksmerprome, Vanvimon
    Panyim, Sakol
    Flegel, Timothy W.
    Sritunyalucksana, Kallaya
    Borwornpinyo, Suparerk
    JOURNAL OF THE WORLD AQUACULTURE SOCIETY, 2022, 53 (03) : 724 - 740
  • [38] Effects of short-hairpin RNA-inhibited β-catenin expression on the growth of human multiple myeloma cells in vitro and in vivo
    Liang, Wenqing
    Yang, Chengwei
    Qian, Yu
    Fu, Qiang
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 422 (04) : 681 - 686
  • [39] Short-hairpin RNAs synthesized by T7 phage polymerase do not induce interferon
    Gondai, Takuma
    Yamaguchi, Kazuya
    Miyano-Kurosaki, Naoko
    Habu, Yuichirou
    Takaku, Hiroshi
    NUCLEIC ACIDS RESEARCH, 2008, 36 (03)
  • [40] Recruitment of RNA polymerase III to its target promoters
    Schramm, L
    Hernandez, N
    GENES & DEVELOPMENT, 2002, 16 (20) : 2593 - 2620