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Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth
BACKGROUND: Transforming Growth Factor-β1 stimulated clone-22 (TSC-22) is assumed to act as a negative growth regulator and tumor suppressor. TSC-22 belongs to a family of putative transcription factors encoded by four distinct loci in mammals. Possible redundancy among the members of the TSC-22/Dip...
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/PMC2253523/ https://www.ncbi.nlm.nih.gov/pubmed/18226226 http://dx.doi.org/10.1186/1471-213X-8-10 |
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author | Gluderer, Silvia Oldham, Sean Rintelen, Felix Sulzer, Andrea Schütt, Corina Wu, Xiaodong Raftery, Laurel A Hafen, Ernst Stocker, Hugo |
author_facet | Gluderer, Silvia Oldham, Sean Rintelen, Felix Sulzer, Andrea Schütt, Corina Wu, Xiaodong Raftery, Laurel A Hafen, Ernst Stocker, Hugo |
author_sort | Gluderer, Silvia |
collection | PubMed |
description | BACKGROUND: Transforming Growth Factor-β1 stimulated clone-22 (TSC-22) is assumed to act as a negative growth regulator and tumor suppressor. TSC-22 belongs to a family of putative transcription factors encoded by four distinct loci in mammals. Possible redundancy among the members of the TSC-22/Dip/Bun protein family complicates a genetic analysis. In Drosophila, all proteins homologous to the TSC-22/Dip/Bun family members are derived from a single locus called bunched (bun). RESULTS: We have identified bun in an unbiased genetic screen for growth regulators in Drosophila. Rather unexpectedly, bun mutations result in a growth deficit. Under standard conditions, only the long protein isoform BunA – but not the short isoforms BunB and BunC – is essential and affects growth. Whereas reducing bunA function diminishes cell number and cell size, overexpression of the short isoforms BunB and BunC antagonizes bunA function. CONCLUSION: Our findings establish a growth-promoting function of Drosophila BunA. Since the published studies on mammalian systems have largely neglected the long TSC-22 protein version, we hypothesize that the long TSC-22 protein is a functional homolog of BunA in growth regulation, and that it is antagonized by the short TSC-22 protein. |
format | Text |
id | pubmed-2253523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22535232008-02-23 Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth Gluderer, Silvia Oldham, Sean Rintelen, Felix Sulzer, Andrea Schütt, Corina Wu, Xiaodong Raftery, Laurel A Hafen, Ernst Stocker, Hugo BMC Dev Biol Research Article BACKGROUND: Transforming Growth Factor-β1 stimulated clone-22 (TSC-22) is assumed to act as a negative growth regulator and tumor suppressor. TSC-22 belongs to a family of putative transcription factors encoded by four distinct loci in mammals. Possible redundancy among the members of the TSC-22/Dip/Bun protein family complicates a genetic analysis. In Drosophila, all proteins homologous to the TSC-22/Dip/Bun family members are derived from a single locus called bunched (bun). RESULTS: We have identified bun in an unbiased genetic screen for growth regulators in Drosophila. Rather unexpectedly, bun mutations result in a growth deficit. Under standard conditions, only the long protein isoform BunA – but not the short isoforms BunB and BunC – is essential and affects growth. Whereas reducing bunA function diminishes cell number and cell size, overexpression of the short isoforms BunB and BunC antagonizes bunA function. CONCLUSION: Our findings establish a growth-promoting function of Drosophila BunA. Since the published studies on mammalian systems have largely neglected the long TSC-22 protein version, we hypothesize that the long TSC-22 protein is a functional homolog of BunA in growth regulation, and that it is antagonized by the short TSC-22 protein. BioMed Central 2008-01-28 /pmc/articles/PMC2253523/ /pubmed/18226226 http://dx.doi.org/10.1186/1471-213X-8-10 Text en Copyright © 2008 Gluderer 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 Article Gluderer, Silvia Oldham, Sean Rintelen, Felix Sulzer, Andrea Schütt, Corina Wu, Xiaodong Raftery, Laurel A Hafen, Ernst Stocker, Hugo Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth |
title | Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth |
title_full | Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth |
title_fullStr | Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth |
title_full_unstemmed | Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth |
title_short | Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth |
title_sort | bunched, the drosophila homolog of the mammalian tumor suppressor tsc-22, promotes cellular growth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253523/ https://www.ncbi.nlm.nih.gov/pubmed/18226226 http://dx.doi.org/10.1186/1471-213X-8-10 |
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