Phosphorylation networks regulating JNK activity in diverse genetic backgrounds

被引:97
作者
Bakal, Chris [1 ,2 ]
Linding, Rune [3 ]
Llense, Flora [4 ]
Heffern, Elleard [2 ]
Martin-Blanco, Enrique [4 ]
Pawson, Tony [5 ]
Perrimon, Norbert [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02215 USA
[3] Inst Canc Res, Cellular & Mol Log Team, London SW3 6JB, England
[4] CSIC, Spanish Council Sci Res, Inst Biol Mol Barcelona, E-08028 Barcelona, Spain
[5] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
关键词
D O I
10.1126/science.1158739
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
Cellular signaling networks have evolved to enable swift and accurate responses, even in the face of genetic or environmental perturbation. Thus, genetic screens may not identify all the genes that regulate different biological processes. Moreover, although classical screening approaches have succeeded in providing parts lists of the essential components of signaling networks, they typically do not provide much insight into the hierarchical and functional relations that exist among these components. We describe a high-throughput screen in which we used RNA interference to systematically inhibit two genes simultaneously in 17,724 combinations to identify regulators of Drosophila JUN NH(2)-terminal kinase (JNK). Using both genetic and phosphoproteomics data, we then implemented an integrative network algorithm to construct a JNK phosphorylation network, which provides structural and mechanistic insights into the systems architecture of JNK signaling.
引用
收藏
页码:453 / 456
页数:4
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