The silent revolution: RNA interference as basic biology, research tool, and therapeutic

被引:248
作者
Dykxhoorn, DM [1 ]
Lieberman, J
机构
[1] Harvard Univ, Sch Med, CBR, Biomed Res Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
来源
ANNUAL REVIEW OF MEDICINE | 2005年 / 56卷
关键词
small interfering RNA; miRNA; posttranscriptional gene silencing gene therapy;
D O I
10.1146/annurev.med.56.082103.104606
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
RNA interference (RNAi) is an evolutionarily conserved mechanism for silencing gene expression. In primitive organisms, RNAi protects the genome from viruses and other insertable genetic elements and regulates gene expression during development. The antisense (guide) strand of short double-stranded RNAs is incorporated into an RNA-induced silencing complex that can either suppress protein expression or direct degradation of messenger RNAs that contain homologous sequence(s). The discovery that RNAi works in mammalian cells has sparked intense investigation into its role in normal mammalian cell function, its use as a tool to understand or screen for genes functioning in cellular pathways in healthy and diseased cells and animals, and its potential for therapeutic gene silencing. RNAi may provide an important new therapeutic modality for treating infection, cancer, neurodegenerative disease, and other illnesses, although in vivo delivery of small interfering RNAs into cells remains a significant obstacle.
引用
收藏
页码:401 / 423
页数:23
相关论文
共 114 条
[41]   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
[42]   Small interfering RNA and gene silencing in transgenic mice and rats [J].
Hasuwa, H ;
Kaseda, K ;
Einarsdottir, T ;
Okabe, M .
FEBS LETTERS, 2002, 532 (1-2) :227-230
[43]   An epi-allelic series of p53 hypomorphs created by stable RNAi produces distinct tumor phenotypes in vivo [J].
Hemann, MT ;
Fridman, JS ;
Zilfou, JT ;
Hernando, E ;
Paddison, PJ ;
Cordon-Cardo, C ;
Hannon, GJ ;
Lowe, SW .
NATURE GENETICS, 2003, 33 (03) :396-400
[44]   Local gene knockdown in the brain using viral-mediated RNA interference [J].
Hommel, JD ;
Sears, RM ;
Georgescu, D ;
Simmons, DL ;
DiLeone, RJ .
NATURE MEDICINE, 2003, 9 (12) :1539-1544
[45]   Embryonic stem cell-specific MicroRNAs [J].
Houbaviy, HB ;
Murray, MF ;
Sharp, PA .
DEVELOPMENTAL CELL, 2003, 5 (02) :351-358
[46]   Expression profiling reveals off-target gene regulation by RNAi [J].
Jackson, AL ;
Bartz, SR ;
Schelter, J ;
Kobayashi, SV ;
Burchard, J ;
Mao, M ;
Li, B ;
Cavet, G ;
Linsley, PS .
NATURE BIOTECHNOLOGY, 2003, 21 (06) :635-637
[47]   Modulation of HIV-1 replication by RNA interference [J].
Jacque, JM ;
Triques, K ;
Stevenson, M .
NATURE, 2002, 418 (6896) :435-438
[48]   ALTERED GENE-EXPRESSION IN PLANTS DUE TO TRANS INTERACTIONS BETWEEN HOMOLOGOUS GENES [J].
JORGENSEN, R .
TRENDS IN BIOTECHNOLOGY, 1990, 8 (12) :340-344
[49]   Small interfering RNAs mediate sequence-independent gene suppression and induce immune activation by signaling through toll-like receptor 3 [J].
Karikó, K ;
Bhuyan, P ;
Capodici, J ;
Weissman, D .
JOURNAL OF IMMUNOLOGY, 2004, 172 (11) :6545-6549
[50]   A conserved siRNA-degrading RNase negatively regulates RNA interference in C-elegans [J].
Kennedy, S ;
Wang, D ;
Ruvkun, G .
NATURE, 2004, 427 (6975) :645-649