Analysis of gene function in somatic mammalian cells using small interfering RNAs

被引:1060
|
作者
Elbashir, SM
Harborth, J
Weber, K
Tuschl, T
机构
[1] Max Planck Inst Biophys Chem, Dept Biochem & Cell Biol, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37077 Gottingen, Germany
关键词
RNA interference; small interfering RNA; posttranscriptional gene silencing; knockdown; double-stranded RNA;
D O I
10.1016/S1046-2023(02)00023-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RNA interference (RNAi) is a highly conserved gene silencing mechanism that uses double-stranded RNA (dsRNA) as a signal to trigger the degradation of homologous mRNA. The mediators of sequence-specific mRNA degradation are 21- to 23-nt small interfering RNAs (siRNAs) generated by ribonuclease III cleavage from longer dsRNAs. Twenty-one-nuclcotide siRNA duplexes trigger specific gene silencing in mammalian somatic cells without activation of the unspecific interferon response. Here we provide a collection of protocols for siRNA-mediated knockdown of mammalian gene expression. Because of the robustness of the siRNA knockdown technology. genomewide analysis of human gene function in cultured cells has now become possible. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:199 / 213
页数:15
相关论文
共 50 条
  • [21] A system for stable expression of short interfering RNAs in mammalian cells
    Brummelkamp, TR
    Bernards, R
    Agami, R
    SCIENCE, 2002, 296 (5567) : 550 - 553
  • [22] Genomewide view of gene silencing by small interfering RNAs
    Chi, JT
    Chang, HY
    Wang, NN
    Chang, DS
    Dunphy, N
    Brown, PO
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) : 6343 - 6346
  • [23] Nonspecific, concentration-dependent stimulation and repression of mammalian gene expression by small interfering RNAs (siRNAs)
    Persengiev, SP
    Zhu, XC
    Green, MR
    RNA, 2004, 10 (01) : 12 - 18
  • [24] Efficient RNAi-induced Protein Knockdown in Somatic Cells Using Diced or Chemically Produced Small Interfering RNAs (siRNA)
    Simiano Tavares, Kaio Cesar
    de Mello e Pinho, Raquel
    Carneiro, Igor de Sa
    de Aguiar, Luis Henrique
    Mendez Calderon, Carlos Enrique
    Martins, Leonardo Tondello
    Ambrosio, Carlos Eduardo
    Maga, Elizabeth Anne
    Bertolini, Marcelo
    Murray, James Donald
    Bertolini, Luciana Relly
    ACTA SCIENTIAE VETERINARIAE, 2012, 40 (03)
  • [25] Effects of small interfering RNAs targeting Fascin on gene expression in oral cancer cells
    Chen, Su-Feng
    Lin, Chi-Yu
    Chang, Yun-Ching
    Li, Jhy-Wei
    Fu, Earl
    Chang, Fei-Ni
    Lin, Yu-Lu
    Nieh, Shin
    JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2009, 38 (09) : 722 - 730
  • [26] RNA interference by expression of short-interfering RNAs and hairpin RNAs in mammalian cells
    Yu, JY
    DeRuiter, SL
    Turner, DL
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) : 6047 - 6052
  • [27] Selective depletion of the Type I, Type II, and Type III isozymes of hexokinase in mammalian cells using small interfering RNAs
    Sui, DX
    Wilson, JE
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (03) : 768 - 773
  • [28] RNA interference and the use of small interfering RNA to study gene function in mammalian systems
    Bantounas, I
    Phylactou, LA
    Uney, JB
    JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2004, 33 (03) : 545 - 557
  • [29] UPAR inhibition in melanoma cells by small interfering RNAs
    Besch, R
    Schuh, T
    Berking, C
    Kammerbauer, C
    Degitz, K
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 123 (02)
  • [30] Transcriptional targeting of small interfering RNAs into cancer cells
    Huynh, Trang
    Walchli, Seastien
    Sioud, Mouldy
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 350 (04) : 854 - 859