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EMBO Rep. 2010 Mar;11(3):201-7. doi: 10.1038/embor.2010.1. Epub 2010 Feb 19.

Transcriptional targets of Drosophila JAK/STAT pathway signalling as effectors of haematopoietic tumour formation.

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1
MRC Centre for Developmental & Biomedical Genetics, The University of Sheffield, Western Bank, Sheffield, UK.

Abstract

Although many signal transduction pathways have been implicated in the development of human disease, the identification of pathway targets and the biological processes that mediate disease progression remains challenging. One such disease-related pathway is the Janus kinase (JAK)/signal transducer and activator of transcription (STAT) cascade whose constitutive misactivation by the JAK2 V617F mutation underlies most human myeloproliferative disorders. Here, we use transcript profiling of Drosophila haemocyte-like cells to identify JAK/STAT target genes, combined with an in vivo model for JAK-induced blood cell overproliferation, to identify the main effectors required for haematopoietic tumour development. The identified human homologues of the Drosophila effectors were tested for potential V617F-mediated transcriptional regulation in human HeLa cells and compared with small interfering RNA-derived data, quantify their role in regulating the proliferation of cancer-derived cell lines. Such an inter-species approach is an effective way to identify factors with conserved functions that might be central to human disease.

PMID:
20168330
PMCID:
PMC2838687
DOI:
10.1038/embor.2010.1
[Indexed for MEDLINE]
Free PMC Article
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