In vivo activity of nuclease-resistant siRNAs

被引:457
作者
Layzer, JM
McCaffrey, AP
Tanner, AK
Huang, Z
Kay, MA
Sullenger, BA [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Surg, Ctr Genet & Cellular Therapies, Durham, NC 27710 USA
[2] Stanford Univ, Sch Med, Dept Pediat, Program Human Gene Therapy, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Program Human Gene Therapy, Stanford, CA 94305 USA
关键词
RNAi; siRNA; modified nucleotides; luciferase;
D O I
10.1261/rna.5239604
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemical modifications have been incorporated into short interfering RNAs (siRNAs) without reducing their ability to inhibit gene expression in mammalian cells grown in vitro. In this study, we begin to assess the potential utility of 2'-modified siRNAs in mammals. We demonstrate that siRNA modified with 2'-flouro (2'-F) pyrimidines are functional in cell culture and have a greatly increased stability and a prolonged half-life in human plasma as compared to 2'-OH containing siRNAs. Moreover, we show that the 2'-F containing siRNAs are functional in mice and can inhibit the expression of a target gene in vivo. However, even though the modified siRNAs have greatly increased resistance to nuclease degradation in plasma, this increase in stability did not translate into enhanced or prolonged inhibitory activity of target gene reduction in mice following tail vein injection. Thus, this study shows that 2'-F modified siRNAs are functional in vivo, but that they are not necessarily more potent than unmodified siRNAs in animals.
引用
收藏
页码:766 / 771
页数:6
相关论文
共 27 条
[1]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[2]   RNA interference in mammalian cells by chemically-modified RNA [J].
Braasch, DA ;
Jensen, S ;
Liu, YH ;
Kaur, K ;
Arar, K ;
White, MA ;
Corey, DR .
BIOCHEMISTRY, 2003, 42 (26) :7967-7975
[3]   siRNA function in RNAi: A chemical modification analysis [J].
Chiu, YL ;
Rana, TM .
RNA, 2003, 9 (09) :1034-1048
[4]   Visualizing gene expression in living mammals using a bioluminescent reporter [J].
Contag, CH ;
Spilman, SD ;
Contag, PR ;
Oshiro, M ;
Eames, B ;
Dennery, P ;
Stevenson, DK ;
Benaron, DA .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (04) :523-531
[5]   Structural variations and stabilising modifications of synthetic siRNAs in mammalian cells [J].
Czauderna, F ;
Fechtner, M ;
Dames, S ;
Aygün, H ;
Klippel, A ;
Pronk, GJ ;
Giese, K ;
Kaufmann, J .
NUCLEIC ACIDS RESEARCH, 2003, 31 (11) :2705-2716
[6]   Killing the messenger: Short RNAs that silence gene expression [J].
Dykxhoorn, DM ;
Novina, CD ;
Sharp, PA .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (06) :457-467
[7]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[8]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[9]   A species of small antisense RNA in posttranscriptional gene silencing in plants [J].
Hamilton, AJ ;
Baulcombe, DC .
SCIENCE, 1999, 286 (5441) :950-952
[10]   An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells [J].
Hammond, SM ;
Bernstein, E ;
Beach, D ;
Hannon, GJ .
NATURE, 2000, 404 (6775) :293-296