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Human 14-3-3 Gamma Protein Results in Abnormal Cell Proliferation in the Developing Eye of Drosophila Melanogaster

Overview
Journal Cell Div
Publisher Biomed Central
Date 2008 Jan 16
PMID 18194556
Citations 3
Authors
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Abstract

Background: 14-3-3 proteins are a family of adaptor proteins that participate in a wide variety of cellular processes. Recent evidence indicates that the expression levels of these proteins are elevated in some human tumors providing circumstantial evidence for their involvement in human cancers. However, the mechanism through which these proteins act in tumorigenesis is uncertain.

Results: To determine whether elevated levels of 14-3-3 proteins may perturb cell growth we overexpressed human 14-3-3 gamma (h14-3-3 gamma) in Drosophila larvae using the heat shock promoter or the GMR-Gal4 driver and then examined the effect that this had on cell proliferation in the eye imaginal discs of third instar larvae. We found that induction of h14-3-3 gamma resulted in the abnormal appearance of replicating cells in the differentiating proneural photoreceptor cells of eye imaginal discs where h14-3-3 gamma was driven by the heat shock promoter. Similarly, we found that driving h14-3-3 gamma expression specifically in developing eye discs with the GMR-Gal4 driver resulted in increased numbers of replicative cells following the morphogenetic furrow. Interestingly, we found that the effects of overexpressing h1433 gamma on eye development were increased in a genetic background where String (cdc25) function was compromised.

Conclusion: Taken together our results indicate that h14-3-3 gamma can promote abnormal cell proliferation and may act through Cdc25. This has important implications for 14-3-3 gamma as an oncogene as it suggests that elevated levels of 14-3-3 may confer a growth advantage to cells that overexpress it.

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References
1.
She Q, Solit D, Ye Q, OReilly K, Lobo J, Rosen N . The BAD protein integrates survival signaling by EGFR/MAPK and PI3K/Akt kinase pathways in PTEN-deficient tumor cells. Cancer Cell. 2005; 8(4):287-97. PMC: 3203692. DOI: 10.1016/j.ccr.2005.09.006. View

2.
Martin D, Brown-Luedi M, Chiquet-Ehrismann R . Tenascin-C signaling through induction of 14-3-3 tau. J Cell Biol. 2003; 160(2):171-5. PMC: 2172641. DOI: 10.1083/jcb.200206109. View

3.
Chan T, Hwang P, Hermeking H, Kinzler K, Vogelstein B . Cooperative effects of genes controlling the G(2)/M checkpoint. Genes Dev. 2000; 14(13):1584-8. PMC: 316737. View

4.
Li W, Skoulakis E, Davis R, Perrimon N . The Drosophila 14-3-3 protein Leonardo enhances Torso signaling through D-Raf in a Ras 1-dependent manner. Development. 1997; 124(20):4163-71. DOI: 10.1242/dev.124.20.4163. View

5.
Thummel C, Boulet A, Lipshitz H . Vectors for Drosophila P-element-mediated transformation and tissue culture transfection. Gene. 1988; 74(2):445-56. DOI: 10.1016/0378-1119(88)90177-1. View