|Title||The Drosophila gene brinker reveals a novel mechanism of Dpp target gene regulation.|
|Publication Type||Journal Article|
|Year of Publication||1999|
|Authors||Jaźwińska, A, Kirov, N, Wieschaus, E, Roth, S, Rushlow, C|
|Date Published||1999 Feb 19|
|Keywords||Animals, Bone Morphogenetic Protein Receptors, Type I, Cloning, Molecular, DNA-Binding Proteins, Drosophila, Drosophila Proteins, Gene Expression Regulation, Developmental, Homeodomain Proteins, Insect Proteins, Molecular Sequence Data, Nerve Tissue Proteins, Phenotype, Promoter Regions, Genetic, Protein-Serine-Threonine Kinases, Receptors, Cell Surface, Receptors, Growth Factor, Repressor Proteins, Sequence Homology, Amino Acid, Signal Transduction, Smad6 Protein, T-Box Domain Proteins, Trans-Activators, Transcription Factors, Wing|
decapentaplegic (dpp), a Drosophila member of the TGFbeta family of secreted molecules, functions as a long-range morphogen in patterning of the embryo and the adult appendages. Dpp signals via the SMAD proteins Mad and Medea. Here we show that in the absence of brinker (brk), Mad is not required for the activation of Dpp target genes that depend on low levels of Dpp. brk encodes a novel protein with features of a transcriptional repressor. brk itself is negatively regulated by Dpp. Dpp signaling might relieve brk's repression of low-level target genes either by transcriptional repression of brk or by antagonizing a repressor function of brk at the target gene promoters.