Brief Communication abstract
Nature Cell Biology 4, 976 - 980 (2002)
Published online: 25 November 2002 | doi:10.1038/ncb887
Pointed and Tramtrack69 establish an EGFR-dependent transcriptional switch to regulate mitosis
Antonio Baonza1,2, Christopher M. Murawsky1,2, Andrew A. Travers1 & Matthew Freeman1
Cell division in animals must be regulated; during development, for example, proliferation often occurs in spatially and temporally restricted patterns1, 2, 3, and loss of mitotic control underlies cancer4. The epidermal growth factor receptor (EGFR) has been implicated extensively in the control of cell proliferation in metazoans5, 6, 7; in addition, hyperactivity of the EGFR and its three relatives, ErbB2–ErbB4, are implicated in many cancers8. But little is known about how these receptor tyrosine kinases regulate the cell cycle. In the developing Drosophila melanogaster imaginal eye disc, there is a single patterned mitosis that sweeps across the eye disc epithelium in the third larval instar9. This 'second mitotic wave' is triggered by EGFR signalling5 and depends on expression of String, the Drosophila homologue of Cdc25 phosphatase, the ultimate regulator of mitosis in all eukaryotic cells10, 11, 12. Here we show that two antagonistic transcriptional regulators, Pointed, an activator, and Tramtrack69, a repressor, directly regulate the transcription of string. The activity of at least one of these regulators, Pointed, is controlled by EGFR signalling. This establishes a molecular mechanism for how intercellular signalling can control string expression, and thereby cell proliferation.
- MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK
- These authors contributed equally to this work
Correspondence to: Andrew A. Travers1 e-mail: AAT@mrc-lmb.cam.ac.uk
Correspondence to: Matthew Freeman1 e-mail: MF1@mrc-lmb.cam.ac.uk
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