Phosphorylation Networks Regulating JNK Activity in Diverse Genetic Backgrounds

Author:

Bakal Chris12345,Linding Rune12345,Llense Flora12345,Heffern Elleard12345,Martin-Blanco Enrique12345,Pawson Tony12345,Perrimon Norbert12345

Affiliation:

1. Department of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02215, USA.

2. Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02215, USA.

3. Cellular & Molecular Logic Team, The Institute for Cancer Research, 237 Fulham Road, London SW3 6JB, UK.

4. Institut de Biologia Molecular de Barcelona, CSIC (Spanish Council for Scientific Research), Parc Científic de Barcelona, 08028 Spain.

5. Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario M5G 1X5, Canada.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference27 articles.

1. Robustness and evolution: concepts, insights and challenges from a developmental model system

2. The JNK signal transduction pathway

3. The control of cell motility and epithelial morphogenesis by Jun kinases

4. Materials and methods are available as supporting material on Science Online.

5. Supplemental tables and files are available at http://genepath.med.harvard.edu/~cbakal/Supplemental.

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