Algorithm for selection of functional siRNA sequences

被引:271
作者
Amarzguioui, M [1 ]
Prydz, H [1 ]
机构
[1] Univ Oslo, Ctr Biotechnol, N-0349 Oslo, Norway
关键词
siRNA; RNAi; duplex instability; asymmetry; GC content; sequence motifs; target sequence selection;
D O I
10.1016/j.bbrc.2004.02.157
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Randomly designed siRNA targeting different positions within the same mRNA display widely differing activities. We have performed a statistical analysis of 46 siRNA, identifying various features of the 19bp duplex that correlate significantly with functionality at the 70% knockdown level and verified these results against an independent data set of 34 siRNA recently reported by others. Features that consistently correlated positively with functionality across the two data sets included an asymmetry in the stability of the duplex ends (measured as the A/U differential of the three terminal basepairs at either end of the duplex) and the motifs S1, A6, and W19. The presence of the motifs U1 or G19 was associated with lack of functionality. A selection algorithm based on these findings strongly differentiated between the two functional groups of siRNA in both data sets and proved highly effective when used to design siRNA targeting new endogenous human genes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1050 / 1058
页数:9
相关论文
共 33 条
[1]
Secondary structure prediction and in vitro accessibility of mRNA as tools in the selection of target sites for ribozymes [J].
Amarzguioui, M ;
Brede, G ;
Babaie, E ;
Grotli, M ;
Sproat, B ;
Prydz, H .
NUCLEIC ACIDS RESEARCH, 2000, 28 (21) :4113-4124
[2]
Tolerance for mutations and chemical modifications in a siRNA [J].
Amarzguioui, M ;
Holen, T ;
Babaie, E ;
Prydz, H .
NUCLEIC ACIDS RESEARCH, 2003, 31 (02) :589-595
[3]
microRNAs: Tiny regulators with great potential [J].
Ambros, V .
CELL, 2001, 107 (07) :823-826
[4]
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
[5]
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
[6]
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
[7]
RNAi in human cells: Basic structural and functional features of small interfering RNA [J].
Chiu, YL ;
Rana, TM .
MOLECULAR CELL, 2002, 10 (03) :549-561
[8]
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
[9]
Functional anatomy of siRNAs for mediating efficient RNAi in Drosophila melanogaster embryo lysate [J].
Elbashir, SM ;
Martinez, J ;
Patkaniowska, A ;
Lendeckel, W ;
Tuschl, T .
EMBO JOURNAL, 2001, 20 (23) :6877-6888
[10]
The activity of siRNA in mammalian cells is related to structural target accessibility: a comparison with antisense oligonucleotides [J].
Far, RKK ;
Sczakiel, G .
NUCLEIC ACIDS RESEARCH, 2003, 31 (15) :4417-4424