Approaches for the sequence-specific knockdown of mRNA

被引:372
作者
Scherer, LJ [1 ]
Rossi, JJ [1 ]
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Div Mol Biol, Duarte, CA 91010 USA
关键词
D O I
10.1038/nbt915
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
Over the past 25 years there have been thousands of published reports describing applications of antisense nucleic acid derivatives for targeted inhibition of gene function. The major classes of antisense agents currently used by investigators for sequence- specific mRNA knockdowns are antisense oligonucleotides (ODNs), ribozymes, DNAzymes and RNA interference (RNAi). Whatever the method, the problems for effective application are remarkably similar: efficient delivery, enhanced stability, minimization of off- target effects and identification of sensitive sites in the target RNAs. These challenges have been in existence from the first attempts to use antisense research tools, and need to be met before any antisense molecule can become widely accepted as a therapeutic agent.
引用
收藏
页码:1457 / 1465
页数:9
相关论文
共 100 条
[1]  
BARTEL D, 2003, NAT CELL BIOL, V5, P489
[2]   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
[3]   COMPARISON OF BINDING OF MIXED RIBOSE DEOXYRIBOSE ANALOGS OF CUCU TO A RIBOZYME AND TO GGAGAA BY EQUILIBRIUM DIALYSIS - EVIDENCE FOR RIBOZYME SPECIFIC INTERACTIONS WITH 2' OH GROUPS [J].
BEVILACQUA, PC ;
TURNER, DH .
BIOCHEMISTRY, 1991, 30 (44) :10632-10640
[4]   The efficacy of small interfering RNAs targeted to the type 1 insulin-like growth factor receptor (IGF1R) is influenced by secondary structure in the IGF1R transcript [J].
Bohula, EA ;
Salisbury, AJ ;
Sohail, M ;
Playford, MP ;
Riedemann, J ;
Southern, EM ;
Macaulay, VM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (18) :15991-15997
[5]   A Hitchhiker's guide to antisense and nonantisense biochemical pathways [J].
Branch, AD .
HEPATOLOGY, 1996, 24 (06) :1517-1529
[6]   Induction of an interferon response by RNAi vectors in mammalian cells [J].
Bridge, AJ ;
Pebernard, S ;
Ducraux, A ;
Nicoulaz, AL ;
Iggo, R .
NATURE GENETICS, 2003, 34 (03) :263-264
[7]   NUCLEOTIDE-SEQUENCE AND NEWLY FORMED PHOSPHODIESTER BOND OF SPONTANEOUSLY LIGATED SATELLITE TOBACCO RINGSPOT VIRUS-RNA [J].
BUZAYAN, JM ;
HAMPEL, A ;
BRUENING, G .
NUCLEIC ACIDS RESEARCH, 1986, 14 (24) :9729-9743
[8]   A NUCLEOTIDE-SEQUENCE REARRANGEMENT DISTINGUISHES 2 ISOLATES OF SATELLITE TOBACCO RINGSPOT VIRUS-RNA [J].
BUZAYAN, JM ;
MCNINCH, JS ;
SCHNEIDER, IR ;
BRUENING, G .
VIROLOGY, 1987, 160 (01) :95-99
[9]   Catalytic DNA: A novel tool for gene suppression [J].
Cairns, MJ ;
Saravolac, EG ;
Sun, LQ .
CURRENT DRUG TARGETS, 2002, 3 (03) :269-279
[10]   Specific inhibition of gene expression by small double-stranded RNAs in invertebrate and vertebrate systems [J].
Caplen, NJ ;
Parrish, S ;
Imani, F ;
Fire, A ;
Morgan, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9742-9747