Mothers against dpp encodes a conserved cytoplasmic protein required in DPP/TGF-β responsive cells
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چکیده
The proteins necessary for signal transduction in cells responding to ligands of the TGF-β family are largely unknown. We have previously identified Mad (Mothers against dpp), a gene that interacts with the TGF-β family member encoded by decapentaplegic (dpp) in Drosophila. Assay of Mad’s role in the DPP-dependent events of embryonic midgut development demonstrates that Mad is required for any response of the visceral mesoderm or endoderm to DPP signals from the visceral mesoderm. Replacement of the normal DPP promoter with a heterologous (hsp70) promoter fails to restore DPP-dependent responses in Mad mutant midguts. Experiments utilizing Mad transgenes regulated by tissue-specific promoters show that MAD is required specifically in cells responding to DPP. Immunohistochemical studies localize MAD to the cytoplasm in all tissues examined. Experiments in Xenopus embryos demonstrate that Drosophila MAD can function in the signaling pathway of BMP-4, a vertebrate homolog of dpp. Based on these results, we propose that Mad is a highly conserved and essential element of the DPP signal transduction pathway.
منابع مشابه
Mothers against dpp encodes a conserved cytoplasmic protein required in DPP/TGF-beta responsive cells.
The proteins necessary for signal transduction in cells responding to ligands of the TGF-beta family are largely unknown. We have previously identified Mad (Mothers against dpp), a gene that interacts with the TGF-beta family member encoded by decapentaplegic (dpp) in Drosophila. Assay of Mad's role in the DPP-dependent events of embryonic midgut development demonstrates that Mad is required fo...
متن کاملMothers against dpp participates in a DDP/TGF-beta responsive serine-threonine kinase signal transduction cascade.
Mothers against dpp (Mad) is the prototype of a family of genes required for signaling by TGF-beta related ligands. In Drosophila, Mad is specifically required in cells responding to Decapentaplegic (DPP) signals. We further specify the role of Mad in DPP-mediated signaling by utilizing tkvQ199D, an activated form of the DPP type I receptor serine-threonine kinase thick veins (tkv). In the embr...
متن کاملMedea is a Drosophila Smad4 homolog that is differentially required to potentiate DPP responses.
Mothers against dpp (Mad) mediates Decapentaplegic (DPP) signaling throughout Drosophila development. Here we demonstrate that Medea encodes a MAD-related protein that functions in DPP signaling. MEDEA is most similar to mammalian Smad4 and forms heteromeric complexes with MAD. Like dpp, Medea is essential for embryonic dorsal/ventral patterning. However, Mad is essential in the germline for oo...
متن کاملMothers against dpp participates in a DPP/TGF-β responsive serine-threonine kinase signal transduction cascade
Stuart J. Newfeld1, Arun Mehra2, Matthew A. Singer1, Jeffrey L. Wrana3, Liliana Attisano2 and William M. Gelbart1,* 1Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA 2Department of Anatomy and Cell Biology, University of Toronto, Toronto, ON, Canada, M5S 1A8 3Program in Developmental Biology, The Hospital for Sick Children, Toronto, ON, Canad...
متن کاملGenetic characterization and cloning of mothers against dpp, a gene required for decapentaplegic function in Drosophila melanogaster.
The decapentaplegic (dpp) gene of Drosophila melanogaster encodes a growth factor that belongs to the transforming growth factor-beta (TGF-beta) superfamily and that plays a central role in multiple cell-cell signaling events throughout development. Through genetic screens we are seeking to identify other functions that act upstream, downstream or in concert with dpp to mediate its signaling ro...
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تاریخ انتشار 1996