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Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster
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. Ho...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246125/ https://www.ncbi.nlm.nih.gov/pubmed/18194556 http://dx.doi.org/10.1186/1747-1028-3-2 |
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author | Hong, Sophia W Qi, Wenqing Brabant, Marc Bosco, Giovanni Martinez, Jesse D |
author_facet | Hong, Sophia W Qi, Wenqing Brabant, Marc Bosco, Giovanni Martinez, Jesse D |
author_sort | Hong, Sophia W |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2246125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22461252008-02-19 Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster Hong, Sophia W Qi, Wenqing Brabant, Marc Bosco, Giovanni Martinez, Jesse D Cell Div Research 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. BioMed Central 2008-01-14 /pmc/articles/PMC2246125/ /pubmed/18194556 http://dx.doi.org/10.1186/1747-1028-3-2 Text en Copyright © 2008 Hong et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Hong, Sophia W Qi, Wenqing Brabant, Marc Bosco, Giovanni Martinez, Jesse D Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster |
title | Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster |
title_full | Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster |
title_fullStr | Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster |
title_full_unstemmed | Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster |
title_short | Human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of Drosophila melanogaster |
title_sort | human 14-3-3 gamma protein results in abnormal cell proliferation in the developing eye of drosophila melanogaster |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246125/ https://www.ncbi.nlm.nih.gov/pubmed/18194556 http://dx.doi.org/10.1186/1747-1028-3-2 |
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