共 30 条
Genome-wide resources of endoribonuclease-prepared short interfering RNAs for specific loss-of-function studies
被引:134
作者:

Kittler, Ralf
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Surendranath, Vineeth
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Heninger, Anne-Kristin
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Slabicki, Mikolaj
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Theis, Mirko
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Putz, Gabriele
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Franke, Kristin
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Caldarelli, Antonio
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Grabner, Hannes
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Kozak, Karol
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Wagner, Jan
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Rees, Effi
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Korn, Bernd
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Frenzel, Corina
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Sachse, Christoph
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Soennichsen, Birte
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Guo, Jie
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Schelter, Janell
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Burchard, Julja
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Linsley, Peter S.
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Jackson, Aimee L.
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Habermann, Bianca
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany

Buchholz, Frank
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机构: Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
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.
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页码:337 / 344
页数:8
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