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Cited by 175

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Mothers against dpp encodes a conserved cytoplasmic protein required in DPP/TGF-β responsive cells

Newfeld, Stuart J., Chartoff, Elena H., Graff, Jonathan M., Melton, Douglas A., Gelbart, William M.·1996·Development

Abstract

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.

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Metadata

Authors
Newfeld, S. J., Chartoff, E. H., Graff, J. M., Melton, D. A., & Gelbart, W. M.
Venue
Development
Published
1996-07-01
Volume
122
Issue
7
Pages
2099-2108
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2110632663
Cited by
175
References
1
FWCI
11.50
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Mothers against dpp encodes a conserved cytoplasmic protein required in DPP/TGF-β responsive cells. https://app.cochat.ai/papers/10.1242/dev.122.7.2099
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Newfeld, S. J., Chartoff, E. H., Graff, J. M., Melton, D. A., & Gelbart, W. M. (1996). Mothers against dpp encodes a conserved cytoplasmic protein required in DPP/TGF-β responsive cells. Development. https://doi.org/10.1242/dev.122.7.2099

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