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Projekt Druckansicht

Functional analysis of JAK/STAT signalling using genome-wide RNAi

Antragsteller Dr. Martin Zeidler
Fachliche Zuordnung Zellbiologie
Förderung Förderung von 2005 bis 2008
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 5446281
 
Erstellungsjahr 2010

Zusammenfassung der Projektergebnisse

We undertook genome wide RNAi screens to identify and characterise regulators of the JAK/STAT signal transduction pathway – a signalling cascade whose mis-regulation is a key factor in the development of many human cancers including a wide range of leukaemias. We describe the RNAi screen itself (published in Nature) as well as studies into pathway function that arose from this screen. These include an analysis of the role of endocytosis / trafficking on JAK/STAT signalling as well as a transcript profiling approach to identify cancer-relevant downstream factors. In addition, this support has contributed to the initial work required for the set up of the Wellcome Trust supported Sheffield RNAi Screening Facility.

Projektbezogene Publikationen (Auswahl)

  • (2005). “Identification of JAK/STAT signalling components by genome-wide RNAi”. Nature 436 871-875
    Müller, P., Kuttenkeuler, D., Gesellchen, V., Zeidler, M.P. and Boutros M.
  • (2008). ‘Identification of JAK/STAT pathway regulators - results from RNAi-based reverse genetic screens’. Seminars in Cell and Developmental Biology 19 360-369
    Müller, P., Boutros, M., Zeidler, M.P.
  • (2008). “JAK/STAT pathway signalling in Drosophila melanogaster”. In: “JAK-STAT Pathway in Disease”, edited by Dr. Anastasis Stephanou, (2008 Landes Bioscience)
    Bina, S. and Zeidler, M.P.
  • (2010). “Negative Regulation of Drosophila JAK/STAT signalling by endocytic trafficking”. J. Cell Sci Sep 14. [Epub ahead of print]
    Vidal, O-M., Bausek, N., Smythe, E., Zeidler, M.P.
    (Siehe online unter https://doi.org/10.1242/jcs.066902)
  • (2010). “Transcriptional targets of Drosophila JAK/STAT pathway signalling as effectors of haematopoietic tumour formation”. EMBO Reports 11(3) 201-207
    Bina, S., Wright, VM., Fisher, KH., Milo, M., Zeidler, MP.
 
 

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