Short hairpin RNA-expressing bacteria elicit RNA interference in mammals

被引:194
作者
Xiang, Shuanglin [1 ]
Fruehauf, Johannes [1 ]
Li, Chiang J. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA 02215 USA
关键词
D O I
10.1038/nbt1211
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA-interference (RNAi) is a potent mechanism, conserved from plants to humans for specific silencing of genes, which holds promise for functional genomics and gene-targeted therapies. Here we show that bacteria engineered to produce a short hairpin RNA (shRNA) targeting a mammalian gene induce trans-kingdom RNAi in vitro and in vivo. Nonpathogenic Escherichia coli were engineered to transcribe shRNAs from a plasmid containing the invasin gene Inv and the listeriolysin O gene HlyA, which encode two bacterial factors needed for successful transfer of the shRNAs into mammalian cells. Upon oral or intravenous administration, E. coli encoding shRNA against CTNNB1 (catenin beta-1) induce significant gene silencing in the intestinal epithelium and in human colon cancer xenografts in mice. These results provide an example of trans-kingdom RNAi in higher organisms and suggest the potential of bacteria-mediated RNAi for functional genomics, therapeutic target validation and development of clinically compatible RNAi-based therapies.
引用
收藏
页码:697 / 702
页数:6
相关论文
共 27 条
[11]   Systematic functional analysis of the Caenorhabditis elegans genome using RNAi [J].
Kamath, RS ;
Fraser, AG ;
Dong, Y ;
Poulin, G ;
Durbin, R ;
Gotta, M ;
Kanapin, A ;
Le Bot, N ;
Moreno, S ;
Sohrmann, M ;
Welchman, DP ;
Zipperlen, P ;
Ahringer, J .
NATURE, 2003, 421 (6920) :231-237
[12]  
Kim SB, 2004, PERITON DIALYSIS INT, V24, P597
[13]   Cytosolic delivery of antisense oligonucleotides by listeriolysin O-containing liposomes [J].
Mathew, E ;
Hardee, GE ;
Bennett, CF ;
Lee, KD .
GENE THERAPY, 2003, 10 (13) :1105-1115
[14]   RNA interference spreading in C-elegans [J].
May, RC ;
Plasterk, RHA .
RNA INTERFERENCE, 2005, 392 :308-315
[16]   OLIGORIBONUCLEOTIDE SYNTHESIS USING T7 RNA-POLYMERASE AND SYNTHETIC DNA TEMPLATES [J].
MILLIGAN, JF ;
GROEBE, DR ;
WITHERELL, GW ;
UHLENBECK, OC .
NUCLEIC ACIDS RESEARCH, 1987, 15 (21) :8783-8798
[17]  
MILLIGAN JF, 1989, METHOD ENZYMOL, V180, P51
[18]   DNA modification and functional delivery into human cells using Escherichia coli DH10B -: art. no. 51 [J].
Narayanan, K ;
Warburton, PE .
NUCLEIC ACIDS RESEARCH, 2003, 31 (09) :e51
[19]   Bacteria as tumour-targeting vectors [J].
Pawelek, JM ;
Low, KB ;
Bermudes, D .
LANCET ONCOLOGY, 2003, 4 (09) :548-556
[20]   Non-pathogenic Escherichia coli versus mesalazine for the treatment of ulcerative colitis:: a randomised trial [J].
Rembacken, BJ ;
Snelling, AM ;
Hawkey, PM ;
Chalmers, DM ;
Axon, ATR .
LANCET, 1999, 354 (9179) :635-639