SANE, a Novel LEM Domain Protein, Regulates Bone Morphogenetic Protein Signaling through Interaction with Smad1
Bone morphogenetic proteins (BMPs) are members of the transforming growth factor-β (TGF-β) superfamily that play important roles in bone formation, embryonic patterning, and epidermal-neural cell fate decisions. BMPs signal through pathway specific mediators such as Smads1 and 5, but the upstream re...
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Veröffentlicht in: | The Journal of biological chemistry 2003-01, Vol.278 (1), p.428-437 |
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Sprache: | eng |
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Zusammenfassung: | Bone morphogenetic proteins (BMPs) are members of the transforming growth factor-β (TGF-β) superfamily that play important roles in bone formation, embryonic patterning, and epidermal-neural cell fate decisions. BMPs signal through pathway specific mediators such as Smads1 and 5, but the upstream regulation of BMP-specific Smads has not been fully characterized. Here we report the identification of SANE (Smad1 AntagonisticEffector), a novel protein with significant sequence similarity to nuclear envelop proteins such as MAN1. SANE binds to Smad1/5 and to BMP type I receptors and regulates BMP signaling. SANE specifically blocks BMP-dependent signaling inXenopus embryos and in a mammalian model of bone formation but does not inhibit the TGF-β/Smad2 pathway. Inhibition of BMP signaling by SANE requires interaction between SANE and Smad1, because a SANE mutant that does not bind Smad1 does not inhibit BMP signaling. Furthermore, inhibition appears to be mediated by inhibition of BMP-induced Smad1 phosphorylation, blocking ligand-dependent nuclear translocation of Smad1. These studies define a new mode of regulation for intracellular BMP/Smad1 signaling. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M210505200 |