Author
Listed:
- Yoichi Kato
(Children's Hospital, Department of Neurology, Harvard Medical School)
- Raymond Habas
(Children's Hospital, Department of Neurology, Harvard Medical School
The National Institute of Child Health and Human Development, NIH)
- Yu Katsuyama
(Children's Hospital, Department of Neurology, Harvard Medical School
University of California)
- Anders M. Näär
(Harvard Medical School, Massachusetts General Hospital Cancer Center)
- Xi He
(Children's Hospital, Department of Neurology, Harvard Medical School)
Abstract
The transforming growth factor β (TGFβ) family of cytokines, including Nodal, Activin and bone morphogenetic protein (BMP), have essential roles in development and tumorigenesis1,2. TGFβ molecules activate the Smad family of signal transducers, which form complexes with specific DNA-binding proteins to regulate gene expression1,2. Two discrete Smad-dependent signalling pathways have been identified: TGFβ, Activin and Nodal signal via the Smad2 (or Smad3)–Smad4 complex, whereas BMP signals via the Smad1–Smad4 complex1,2. How distinct Smad complexes regulate specific gene expression is not fully understood. Here we show that ARC105, a component of the activator-recruited co-factor (ARC)3 complex or the metazoan Mediator complex, is essential for TGFβ/Activin/Nodal/Smad2/3 signal transduction. Expression of ARC105 stimulates Activin/Nodal/Smad2 signalling in Xenopus laevis embryos, inducing axis duplication and mesendoderm differentiation, and enhances TGFβ response in human cells. Depletion of ARC105 inhibits TGFβ/Activin/Nodal/Smad2/3 signalling and Xenopus axis formation, but not BMP/Smad1 signalling. ARC105 protein binds to Smad2/3–Smad4 in response to TGFβ and is recruited to Activin/Nodal-responsive promoters in chromatin in a Smad2-dependent fashion. Thus ARC105 is a specific and key ARC/Mediator component linking TGFβ/Activin/Nodal/Smad2/3 signalling to transcriptional activation.
Suggested Citation
Yoichi Kato & Raymond Habas & Yu Katsuyama & Anders M. Näär & Xi He, 2002.
"A component of the ARC/Mediator complex required for TGFβ/Nodal signalling,"
Nature, Nature, vol. 418(6898), pages 641-646, August.
Handle:
RePEc:nat:nature:v:418:y:2002:i:6898:d:10.1038_nature00969
DOI: 10.1038/nature00969
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