A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

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Citation Huang, H., Potter, C.J., Tao, W., Li, D.M., Brogiolo, W., Hafen, E., Sun, H., Xu, T. (1999). PTEN affects cell size, cell proliferation and apoptosis during Drosophila eye development.  Development 126(23): 5365--5372.
FlyBase ID FBrf0111917
Type of publication Research paper
Offprint Available Yes
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PubMed ID 10556061
PubMed Abstract Mutations in the tumor suppressor gene PTEN (MMAC1/TEP1) are associated with a large number of human cancers and several autosomal-dominant disorders. Mice mutant for PTEN die at early embryonic stages and the mutant embryonic fibroblasts display decreased sensitivity to cell death. Overexpression of PTEN in different mammalian tissue culture cells affects various processes including cell proliferation, cell death and cell migration. We have characterized the Drosophila PTEN gene and present evidence that both inactivation and overexpression of PTEN affect cell size, while overexpression of PTEN also inhibits cell cycle progression at early mitosis and promotes cell death during eye development in a context-dependent manner. Furthermore, we have shown that PTEN acts in the insulin signaling pathway and all signals from the insulin receptor can be antagonized by either Drosophila or human PTEN, suggesting a potential means for alleviating symptoms associated with altered insulin signaling.
Biosis 2000.89275
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Language of publication English
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Abbreviation Development
Title Development
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Volume range 99-
Year range 1987-
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Place of publication Cambridge
Language of publication English
ISBN/ISSN 0950-1991
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