◀ Back to SMAD1
BMPR2 — SMAD1
Pathways - manually collected, often from reviews:
-
NCI Pathway Database BMP receptor signaling:
BMP6/BMPR2/BMPR1A-1B complex (BMP6-BMPR2-BMPR1A_BMPR1B)
→
SMAD1 (SMAD1)
(modification, activates)
Ebisawa et al., J Cell Sci 1999
Evidence: assay
-
NCI Pathway Database ALK1 signaling events:
BMP9/BMPR2/Endoglin/ALK1 (dimer) complex (GDF2-ACVRL1-ENG-BMPR2)
→
SMAD1-5-8-active (SMAD1/SMAD9/SMAD5)
(modification, activates)
Scharpfenecker et al., J Cell Sci 2007, Macías-Silva et al., J Biol Chem 1998, Chen et al., J Biol Chem 1999
Evidence: assay
-
NCI Pathway Database ALK1 signaling events:
BMP9/BMPR2/Endoglin/ALK1 (dimer) complex (GDF2-ACVRL1-ENG-BMPR2)
→
SMAD1-5-8 (SMAD1/SMAD9/SMAD5)
(modification, activates)
Scharpfenecker et al., J Cell Sci 2007, Macías-Silva et al., J Biol Chem 1998, Chen et al., J Biol Chem 1999
Evidence: assay
-
NCI Pathway Database ALK2 signaling events:
BMP7/BMPR2/ALK2 (dimer) complex (BMP7-ACVR1-BMPR2)
→
SMAD1-5-8 (SMAD1/SMAD9/SMAD5)
(modification, activates)
Macías-Silva et al., J Biol Chem 1998, Chen et al., J Biol Chem 1999
Evidence: assay, physical interaction
-
NCI Pathway Database BMP receptor signaling:
BMP2-4/BMPR2/BMPR1A-1B/RGM/ENDOFIN/GADD34/PP1CA complex (BMP4_BMP2-BMPR2-BMPR1A_BMPR1B-RGMB_RGMA_HFE2-ZFYVE16-PPP1CA-PPP1R15A)
→
ENDOFIN/SMAD1 complex (ZFYVE16-SMAD1)
(modification, collaborate)
Babitt et al., J Biol Chem 2005, Shi et al., J Cell Sci 2007, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997
Evidence: mutant phenotype, assay, physical interaction, other species
-
NCI Pathway Database BMP receptor signaling:
BMP2-4/BMPR2/BMPR1A-1B/RGM/ENDOFIN/GADD34/PP1CA complex (BMP4_BMP2-BMPR2-BMPR1A_BMPR1B-RGMB_RGMA_HFE2-ZFYVE16-PPP1CA-PPP1R15A)
→
SMAD1 (SMAD1)
(modification, collaborate)
Babitt et al., J Biol Chem 2005, Shi et al., J Cell Sci 2007, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997
Evidence: mutant phenotype, assay, physical interaction, other species
-
NCI Pathway Database BMP receptor signaling:
ENDOFIN/SMAD1 complex (ZFYVE16-SMAD1)
→
BMP2-4/BMPR2/BMPR1A-1B/RGM complex (BMP4_BMP2-BMPR2-BMPR1A_BMPR1B-RGMB_RGMA_HFE2)
(modification, collaborate)
Babitt et al., J Biol Chem 2005, Shi et al., J Cell Sci 2007, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997
Evidence: mutant phenotype, assay, physical interaction, other species
-
NCI Pathway Database BMP receptor signaling:
SMAD1 (SMAD1)
→
BMP2-4/BMPR2/BMPR1A-1B/RGM complex (BMP4_BMP2-BMPR2-BMPR1A_BMPR1B-RGMB_RGMA_HFE2)
(modification, collaborate)
Babitt et al., J Biol Chem 2005, Shi et al., J Cell Sci 2007, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997
Evidence: mutant phenotype, assay, physical interaction, other species
-
NCI Pathway Database BMP receptor signaling:
SMAD1 (SMAD1)
→
BMP2-4/BMPR2/BMPR1A-1B/RGM complex (BMP4_BMP2-BMPR2-BMPR1A_BMPR1B-RGMB_RGMA_HFE2)
(modification, collaborate)
Murakami et al., Mol Biol Cell 2003, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997, Imamura et al., Nature 1997
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database BMP receptor signaling:
SMAD1 (SMAD1)
→
BMP2-4/BMPR2/BMPR1A-1B/RGM/SMAD7/SMURF1 complex (BMP4_BMP2-BMPR2-BMPR1A_BMPR1B-RGMB_RGMA_HFE2-SMAD7-SMURF1)
(modification, collaborate)
Murakami et al., Mol Biol Cell 2003, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997, Imamura et al., Nature 1997
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database BMP receptor signaling:
BMP7/BMPR2/BMPR1A-1B/SMAD6/SMURF1 complex (BMP7-BMPR2-BMPR1A_BMPR1B-SMAD6-SMURF1)
→
SMAD1 (SMAD1)
(modification, collaborate)
Murakami et al., Mol Biol Cell 2003, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997, Imamura et al., Nature 1997
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database BMP receptor signaling:
SMAD1 (SMAD1)
→
BMP7/BMPR2/BMPR1A-1B complex (BMP7-BMPR2-BMPR1A_BMPR1B)
(modification, collaborate)
Murakami et al., Mol Biol Cell 2003, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997, Imamura et al., Nature 1997
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database ALK1 signaling events:
BMP9/BMPR2/Endoglin/ALK1 (dimer)/CK2B complex (GDF2-ACVRL1-CSNK2B-ENG-BMPR2)
→
SMAD1-5-8 (SMAD1/SMAD9/SMAD5)
(modification, activates)
Lee et al., FASEB J 2009, Macías-Silva et al., J Biol Chem 1998
Evidence: mutant phenotype
-
Reactome Reaction:
BMPR2
→
SMAD1
(reaction)
Shi et al., J Cell Sci 2007, Hoodless et al., Cell 1996, Lagna et al., Nature 1996, Kretzschmar et al., Genes Dev 1997
-
Reactome Reaction:
BMPR2
→
SMAD1
(indirect_complex)
Shi et al., J Cell Sci 2007, Hoodless et al., Cell 1996, Kretzschmar et al., Genes Dev 1997
-
WikiPathways Heart Development:
BMPR2/BMPR1A
→
SMAD1
(activation)
Text-mined interactions from Literome
Yu et al., J Biol Chem 2008
:
Although signaling via BMPRII or ActRIIa transiently activated SMAD1/5/8, only
BMPRII signaling
led to persistent
SMAD1/5/8 activation and sustained increases in Id1 mRNA and protein expression
Graham et al., Prostate 2009
(Neoplasm Metastasis...) :
Notably, the activation of
BMPRII by BMP-2 is
required for modulation of
Smad activation by NF-kappaB in PC cells
Johnson et al., J Neuropathol Exp Neurol 2009
(Meningeal Neoplasms...) :
In this study, frozen tissues from 26 World Health Organization Grades I to III meningiomas were analyzed by Western blot for BMP-2/4, BMPR IA, and
BMPR II , and
activation of downstream
p-Smad1 , p38 mitogen activated protein kinase ( MAPK ), and p44/42 MAPK signaling molecules
Yang et al., Ann N Y Acad Sci 2010
(Bone Diseases, Developmental) :
Thus, osteoblast targeted expression of dominant negative
BMPRII leads to inhibited
Smad1 phosphorylation, delayed skeletal development, and decreased bone formation in the adult mice ... This study provides an in vivo tool to study the
role of
BMPRII in
BMP/Smad signaling and the regulation of this pathway by PTH and Wnts
Breen et al., PloS one 2013
(Neoplasm Invasiveness...) :
In contrast
BMPRII regulates
Smad1 in a biphasic manner, promoting Smad1 signaling through its kinase domain but suppressing it through its cytoplasmic tail