Combinatorial RNAi for quantitative protein network analysis

被引:46
作者
Sahin, Ozgur
Loebke, Christian
Korf, Ulrike
Appelhans, Heribert
Sueltmann, Holger
Poustka, Annemarie
Wiemann, Stefan
Arlt, Dorit
机构
[1] Deutsch Krebsforschungszentrum, Div Mol Genome Anal, D-69120 Heidelberg, Germany
[2] Inst Immunol & Mol Genet, D-76133 Karlsruhe, Germany
关键词
combinatorial protein knockdown; reverse-phase protein arrays; signaling pathways; cross-talk; systems biology;
D O I
10.1073/pnas.0606827104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The elucidation of cross-talk events between intersecting signaling pathways is one main challenge in biological research. The complexity of protein networks, composed of different pathways, requires novel strategies and techniques to reveal relevant interrelations. Here, we established a combinatorial RNAi strategy for systematic single, double, and triple knockdown, and we measured the residual mRNAs and proteins quantitatively by quantitative real-time PCR and reverse-phase protein arrays, respectively, as a prerequisite for data analysis. Our results show that the parallel knockdown of at least three different genes is feasible while keeping both untargeted silencing and cytotoxicity low. The technique was validated by investigating the interplay of tyrosine kinase receptor ErbB2 and its downstream targets Akt-1 and MEK1 in cell invasion. This experimental approach combines multiple gene knockdown with a subsequent quantitative validation of reduced protein expression and is a major advancement toward the analysis of signaling pathways in systems biology.
引用
收藏
页码:6579 / 6584
页数:6
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