Genome-wide resources of endoribonuclease-prepared short interfering RNAs for specific loss-of-function studies

被引:134
作者
Kittler, Ralf
Surendranath, Vineeth
Heninger, Anne-Kristin
Slabicki, Mikolaj
Theis, Mirko
Putz, Gabriele
Franke, Kristin
Caldarelli, Antonio
Grabner, Hannes
Kozak, Karol
Wagner, Jan
Rees, Effi
Korn, Bernd
Frenzel, Corina
Sachse, Christoph
Soennichsen, Birte
Guo, Jie
Schelter, Janell
Burchard, Julja
Linsley, Peter S.
Jackson, Aimee L.
Habermann, Bianca
Buchholz, Frank
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] Scion Comp Innovat GmbH, D-01307 Dresden, Germany
[3] Technol Dev Studio, D-01307 Dresden, Germany
[4] RZPD Ressourcenzentrum Genomforsch, D-69120 Heidelberg, Germany
[5] Cenix BioSci GmbH, D-01307 Dresden, Germany
[6] Rosetta Inpharmat LLC, Kirkland, WA 98034 USA
关键词
D O I
10.1038/NMETH1025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RNA interference (RNAi) has become an important technique for loss-of-gene-function studies in mammalian cells. To achieve reliable results in an RNAi experiment, efficient and specific silencing triggers are required. Here we present genome-wide data sets for the production of endoribonuclease-prepared short interfering RNAs (esiRNAs) for human, mouse and rat. We used an algorithm to predict the optimal region for esiRNA synthesis for every protein-coding gene of these three species. We created a database, RiDDLE, for retrieval of target sequences and primer information. To test this in silico resource experimentally, we generated 16,242 esiRNAs that can be used for RNAi screening in human cells. Comparative analyses with chemically synthesized siRNAs demonstrated a high silencing efficacy of esiRNAs and a 12-fold reduction of downregulated off-target transcripts as detected by microarray analysis. Hence, the presented esiRNA libraries offer an efficient, cost-effective and specific alternative to presently available mammalian RNAi resources.
引用
收藏
页码:337 / 344
页数:8
相关论文
共 30 条
[1]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[2]   shRNA libraries and their use in cancer genetics [J].
Bernards, Rene ;
Brummelkamp, Thijn R. ;
Beijersbergen, Roderick L. .
NATURE METHODS, 2006, 3 (09) :701-706
[3]   3′ UTR seed matches, but not overall identity, are associated with RNAi off-targets [J].
Birmingham, A ;
Anderson, EM ;
Reynolds, A ;
Ilsley-Tyree, D ;
Leake, D ;
Fedorov, Y ;
Baskerville, S ;
Maksimova, E ;
Robinson, K ;
Karpilow, J ;
Marshall, WS ;
Khvorova, A .
NATURE METHODS, 2006, 3 (03) :199-204
[4]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[5]   Enzymatically prepared RNAi libraries [J].
Buchholz, Frank ;
Kittler, Ralf ;
Slabicki, Mikolaj ;
Theis, Mirko .
NATURE METHODS, 2006, 3 (09) :696-700
[6]   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
[7]   Unlocking the potential of the human genome with RNA interference [J].
Hannon, GJ ;
Rossi, JJ .
NATURE, 2004, 431 (7006) :371-378
[8]   siRNA target site secondary structure predictions using local stable substructures [J].
Heale, BSE ;
Soifer, HS ;
Bowers, C ;
Rossi, JJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (03) :1-10
[9]   DEQOR: a web-based tool for the design and quality control of siRNAs [J].
Henschel, A ;
Buchholz, F ;
Habermann, B .
NUCLEIC ACIDS RESEARCH, 2004, 32 :W113-W120
[10]   Expression profiling using microarrays fabricated by an ink-jet oligonucleotide synthesizer [J].
Hughes, TR ;
Mao, M ;
Jones, AR ;
Burchard, J ;
Marton, MJ ;
Shannon, KW ;
Lefkowitz, SM ;
Ziman, M ;
Schelter, JM ;
Meyer, MR ;
Kobayashi, S ;
Davis, C ;
Dai, HY ;
He, YDD ;
Stephaniants, SB ;
Cavet, G ;
Walker, WL ;
West, A ;
Coffey, E ;
Shoemaker, DD ;
Stoughton, R ;
Blanchard, AP ;
Friend, SH ;
Linsley, PS .
NATURE BIOTECHNOLOGY, 2001, 19 (04) :342-347