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Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila
BACKGROUND: The TSC-22 domain family (TSC22DF) consists of putative transcription factors harboring a DNA-binding TSC-box and an adjacent leucine zipper at their carboxyl termini. Both short and long TSC22DF isoforms are conserved from flies to humans. Whereas the short isoforms include the tumor su...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871527/ https://www.ncbi.nlm.nih.gov/pubmed/20149264 http://dx.doi.org/10.1186/jbiol216 |
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author | Gluderer, Silvia Brunner, Erich Germann, Markus Jovaisaite, Virginija Li, Changqing Rentsch, Cyrill A Hafen, Ernst Stocker, Hugo |
author_facet | Gluderer, Silvia Brunner, Erich Germann, Markus Jovaisaite, Virginija Li, Changqing Rentsch, Cyrill A Hafen, Ernst Stocker, Hugo |
author_sort | Gluderer, Silvia |
collection | PubMed |
description | BACKGROUND: The TSC-22 domain family (TSC22DF) consists of putative transcription factors harboring a DNA-binding TSC-box and an adjacent leucine zipper at their carboxyl termini. Both short and long TSC22DF isoforms are conserved from flies to humans. Whereas the short isoforms include the tumor suppressor TSC-22 (Transforming growth factor-β1 stimulated clone-22), the long isoforms are largely uncharacterized. In Drosophila, the long isoform Bunched A (BunA) acts as a growth promoter, but how BunA controls growth has remained obscure. RESULTS: In order to test for functional conservation among TSC22DF members, we expressed the human TSC22DF proteins in the fly and found that all long isoforms can replace BunA function. Furthermore, we combined a proteomics-based approach with a genetic screen to identify proteins that interact with BunA. Madm (Mlf1 adapter molecule) physically associates with BunA via a conserved motif that is only contained in long TSC22DF proteins. Moreover, Drosophila Madm acts as a growth-promoting gene that displays growth phenotypes strikingly similar to bunA phenotypes. When overexpressed, Madm and BunA synergize to increase organ growth. CONCLUSIONS: The growth-promoting potential of long TSC22DF proteins is evolutionarily conserved. Furthermore, we provide biochemical and genetic evidence for a growth-regulating complex involving the long TSC22DF protein BunA and the adapter molecule Madm. See minireview at http://jbiol.com/content/9/1/8. |
format | Text |
id | pubmed-2871527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28715272010-05-17 Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila Gluderer, Silvia Brunner, Erich Germann, Markus Jovaisaite, Virginija Li, Changqing Rentsch, Cyrill A Hafen, Ernst Stocker, Hugo J Biol Research article BACKGROUND: The TSC-22 domain family (TSC22DF) consists of putative transcription factors harboring a DNA-binding TSC-box and an adjacent leucine zipper at their carboxyl termini. Both short and long TSC22DF isoforms are conserved from flies to humans. Whereas the short isoforms include the tumor suppressor TSC-22 (Transforming growth factor-β1 stimulated clone-22), the long isoforms are largely uncharacterized. In Drosophila, the long isoform Bunched A (BunA) acts as a growth promoter, but how BunA controls growth has remained obscure. RESULTS: In order to test for functional conservation among TSC22DF members, we expressed the human TSC22DF proteins in the fly and found that all long isoforms can replace BunA function. Furthermore, we combined a proteomics-based approach with a genetic screen to identify proteins that interact with BunA. Madm (Mlf1 adapter molecule) physically associates with BunA via a conserved motif that is only contained in long TSC22DF proteins. Moreover, Drosophila Madm acts as a growth-promoting gene that displays growth phenotypes strikingly similar to bunA phenotypes. When overexpressed, Madm and BunA synergize to increase organ growth. CONCLUSIONS: The growth-promoting potential of long TSC22DF proteins is evolutionarily conserved. Furthermore, we provide biochemical and genetic evidence for a growth-regulating complex involving the long TSC22DF protein BunA and the adapter molecule Madm. See minireview at http://jbiol.com/content/9/1/8. BioMed Central 2010 2010-02-11 /pmc/articles/PMC2871527/ /pubmed/20149264 http://dx.doi.org/10.1186/jbiol216 Text en Copyright ©2010 Gluderer et al.; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research article Gluderer, Silvia Brunner, Erich Germann, Markus Jovaisaite, Virginija Li, Changqing Rentsch, Cyrill A Hafen, Ernst Stocker, Hugo Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila |
title | Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila |
title_full | Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila |
title_fullStr | Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila |
title_full_unstemmed | Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila |
title_short | Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila |
title_sort | madm (mlf1 adapter molecule) cooperates with bunched a to promote growth in drosophila |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871527/ https://www.ncbi.nlm.nih.gov/pubmed/20149264 http://dx.doi.org/10.1186/jbiol216 |
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