Reference Report
| Reference | |||
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| Citation | Gluderer, S., Oldham, S., Rintelen, F., Sulzer, A., Schütt, C., Wu, X., Raftery, L.A., Hafen, E., Stocker, H. (2008). Bunched, the Drosophila homolog of the mammalian tumor suppressor TSC-22, promotes cellular growth. BMC Dev. Biol. 8(): 10. (Export to RIS) | ||
| FlyBase ID | FBrf0205279 | ||
| Publication Type | Research paper | ||
| PubMed ID | 18226226 | ||
| PubMed Abstract | Transforming Growth Factor-beta1 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).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.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. | ||
| DOI | 10.1186/1471-213X-8-10 | ||
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| Language of Publication | English | ||
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| Publication Type | Journal | ||
| Abbreviation | BMC Dev. Biol. | ||
| Title | BMC Developmental Biology | ||
| Publication Year | 2002 | ||
| ISBN/ISSN | 1471-213X | ||
Data from Reference
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Aberrations (3)
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Alleles (36)
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Constructs (10)
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Genes (3)
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Insertions (7)
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Natural transposons (1)
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