TGF beta signaling pathway
The Transforming growth factor beta (TGFβ) signaling pathway is involved in many cellular processes in both the adult organism and the developing
embryoincluding cell growth, cell differentiation, apoptosis, cellular homeostasis and other cellular functions. In spite of the wide range of cellular processes that the TGFβ signaling pathway regulates, the process is relatively simple. TGFβ superfamily ligands bind to a type II receptor, which recruits and phosphorylates a type I receptor. The type I receptor then phosphorylates receptor-regulated SMADs ( R-SMADs) which can now bind the coSMAD SMAD4. R-SMAD/coSMAD complexes accumulate in the nucleus where they act as transcription factors and participate in the regulation of target gene expression.
The TGF Beta superfamily of ligands include: Bone morphogenetic proteins (BMPs), Growth and differentiation factors (GDFs), Anti-müllerian hormone (AMH),
Activin, Nodal and TGFβ'scite web|url=http://www.expasy.org/cgi-bin/nicedoc.pl?PS00250 |title=Prosite Documentation PDOC00223 |accessdate=2006-07-01 |accessmonthday= |accessyear= |author= |last= |first= |authorlink= |coauthors= |date= |year= |month= |format= |work= |publisher= |pages= |language= |archiveurl= |archivedate= ] . Signaling begins with the binding of a TGF beta superfamily ligand to a TGF beta type II receptor. The type II receptor is a serine/threonine receptor kinase, which catalyses the phosphorylationof the Type I receptor. Each class of ligand binds to a specific type II receptor cite book
first = Bruce
coauthors = Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, Peter Walter
title = Molecular Biology of the Cell
publisher = Garland Science
location = New York, NY
id = ISBN 0-8153-3218-1] .In mammals there are seven known type II receptors and five type I receptorscite journal
author=Munir S, Xu G, Wu Y, Yang B, Lala PK, Peng C |title=Nodal and ALK7 inhibit proliferation and induce apoptosis in human trophoblast cells |journal=J. Biol. Chem. |volume=279 |issue=30 |pages=31277–86 |year=2004 |month=Jul |pmid=15150278 |doi=10.1074/jbc.M400641200 |url=http://www.jbc.org/cgi/content/full/279/30/31277] .
There are three activins:
Activin A, Activin Band Activin AB. Activins are involved in embryogenesis and osteogenesis. They also regulate many hormonesincluding pituitary, gonadal and hypothalamichormones as well as insulin. They are also nerve cellsurvival factors.
The BMPs bind to the Bone morphogenetic protein receptor type-2 (BMPR2). They are involved in a multitude of cellular functions including osteogenesis,
cell differentiation, anterior/posterior axis specification, growth, and homeostasis.
The TGF beta family include:
TGFβ1, TGFβ2, TGFβ3. Like the BMPS, TGF betas are involved in embryogenesis and cell differentiation, but they are also involved in apoptosis, as well as other functions. They bind to TGF-beta receptor type-2(TGFBR2).
Receptor recruitment and phosphorylation
The TGF beta ligand binds to a type II receptor dimer, which recruits a type I receptor dimer forming a hetero-tetrameric complex with the ligandcite journal
author=Wrana JL, Attisano L, Cárcamo J, "et al" |title=TGF beta signals through a heteromeric protein kinase receptor complex |journal=Cell |volume=71 |issue=6 |pages=1003–14 |year=1992 |month=Dec |pmid=1333888 |doi= |url=http://linkinghub.elsevier.com/retrieve/pii/0092-8674(92)90395-S] . These receptors are serine/threonine kinase receptors. They have a
cysteinerich extracellular domain, a transmembrane domain and a cytoplasmic serine/threonine rich domain. The GS domainof the type I receptor consists of a series of about thirty serine- glycinerepeatscite web|url=http://www.sanger.ac.uk/cgi-bin/Pfam/getacc?PF08515 |title=Pfam entry TGF_beta_GS |accessdate=2006-07-01 |accessmonthday= |accessyear= |author= |last= |first= |authorlink= |coauthors= |date= |year= |month= |format= |work= |publisher= |pages= |language= |archiveurl= |archivedate=] . The binding of a TGF beta family ligand causes the rotation of the receptors so that their cytoplasmic kinase domains are arranged in a catalytically favorable orientation. The Type II receptor phosphorylates serineresidues of the Type I receptor, which activates the protein.
There are five receptor regulated SMADs:
SMAD1, SMAD2, SMAD3, SMAD5and SMAD9. There are essentially two intracellular pathways involving these R-SMADs. TGF beta's, Activins and Nodals are mediated by SMAD2 and SMAD3, while BMPs, GDFs and AMH are mediated by SMAD1, SMAD5and SMAD9. The binding of the R-SMAD to the type I receptor is mediated by a zinc double finger FYVE domain containing protein. Two such proteins that mediate the TGF beta pathway include SARA (The SMAD anchor for receptor activation) and HGS (Hepatocyte growth factor-regulated tyrosine kinase substrate).
SARA is present in an early
endosomewhich, by clathrin-mediated endocytosis, internalizes the receptor complexcite journal
author=Runyan CE, Schnaper HW, Poncelet AC |title=The role of internalization in transforming growth factor beta1-induced Smad2 association with Smad anchor for receptor activation (SARA) and Smad2-dependent signaling in human mesangial cells |journal=J. Biol. Chem. |volume=280 |issue=9 |pages=8300–8 |year=2005 |month=Mar |pmid=15613484 |doi=10.1074/jbc.M407939200 |url=] . SARA recruits an
R-SMAD. SARA permits the binding of the R-SMAD to the L45 region of the Type I receptor [cite journal
author=Moustakas A |title=Smad signalling network |journal=J. Cell. Sci. |volume=115 |issue=Pt 17 |pages=3355–6 |year=2002 |month=Sep |pmid=12154066 |doi= |url=http://jcs.biologists.org/cgi/content/full/115/17/3355] . SARA orients the R-SMAD such that serine residue on its
C-terminusfaces the catalytic region of the Type I receptor. The Type I receptor phosphorylates the serine residue of the R-SMAD. Phosphorylation induces a conformational change in the MH2 domain of the R-SMAD and its subsequent dissociation from the receptor complex and SARA [cite journal
author=Souchelnytskyi S, Rönnstrand L, Heldin CH, ten Dijke P |title=Phosphorylation of Smad signaling proteins by receptor serine/threonine kinases |journal=Methods Mol. Biol. |volume=124 |issue= |pages=107–20 |year=2001 |pmid=11100470 |doi= |url=] .
The phosphorylated RSMAD has a high affinity for a coSMAD (eg.
SMAD4) and forms a complex with one. The phosphate group does not act as a docking site for coSMAD, rather the phosphorylation opens up an amino acid stretch allowing interaction.
The phosphorylated RSMAD/coSMAD complex enters the nucleus where it binds transcription promoters/cofactors and causes the transcription of DNA.
Bone morphogenetic proteins cause the transcription of
mRNAs involved in osteogenesis, neurogenesis, and ventral mesoderm specification.
TGF betas cause the transcription of mRNAs involved in
apoptosis, extracellular matrixneogenesis and immunosuppression. It is also involved in G1 arrest in the cell cycle.
Activin causes the transcription of mRNAs involved in
gonadal growth, embryo differentiation and placenta formation.
Nodal causes the transcription of mRNAs involved in left and right axis specification, and
The TGF beta signaling pathway is involved in a wide range of cellular process and subsequently is very heavily regulated. There are a variety of mechanisms that the pathway is modulated both positively and negatively: There are agonists for ligands and R-SMADs; there are decoy receptors; and R-SMADs and receptors are ubiquitinated.
chordinand noggin are antagonistsof BMP's. They bind BMP's preventing the binding of the ligand to the receptor. It has been demonstrated that Chordin and Noggin dorsalize mesoderm. They are both found in the dorsal lip of " Xenopus" and convert otherwise epidermis specified tissue into neural tissue (see neurulation). Noggin plays a key role in cartilage and bone patterning. Mice Noggin-/- have excess cartilage and lacked joint formationcite journal
author=Massagué J, Chen YG |title=Controlling TGF-beta signaling |journal=Genes Dev. |volume=14 |issue=6 |pages=627–44 |year=2000 |month=Mar |pmid=10733523 |doi= |url=http://intl.genesdev.org/cgi/content/full/14/6/627#B65] .
Members of the DAN family of proteins also antagonize TGF beta family members. They include Cerberus, DAN, and Gremlin. These proteins contain nine conserved
cysteines which can form disulfide bridges. It is believed that DAN antagonizes GDF5, GDF6and GDF7. Follistatininhibits Activin, which it binds. It directly affects follicle-stimulating hormone(FSH) secretion. Follistatin also is implicated in prostate cancers where mutations in its gene may preventing it from acting on activin which has anti-proliferative properties.
Lefty is a regulator of TGFβ and is involved in the axis patterning during embryogenesis. It is also a member of the TGF superfamily of proteins. It is asymmetrically expressed in the left side of murine embryos and subsequently plays a role in left-right specification. Lefty acts by preventing the phosphorylation of R-SMADs. It does so through a constitutively active TGFβ type I receptor and through a process downstream of its activationcite journal
author=Ulloa L, Tabibzadeh S |title=Lefty inhibits receptor-regulated Smad phosphorylation induced by the activated transforming growth factor-beta receptor |journal=J. Biol. Chem. |volume=276 |issue=24 |pages=21397–404 |year=2001 |month=Jun |pmid=11278746 |doi=10.1074/jbc.M010783200 |url=http://www.jbc.org/cgi/content/full/276/24/21397] .
The Transforming growth factor receptor 3 (TGFBR3) is the most abundant of the TGF-β receptors yetcite journal
author=Blobe GC, Liu X, Fang SJ, How T, Lodish HF |title=A novel mechanism for regulating transforming growth factor beta (TGF-beta) signaling. Functional modulation of type III TGF-beta receptor expression through interaction with the PDZ domain protein, GIPC |journal=J. Biol. Chem. |volume=276 |issue=43 |pages=39608–17 |year=2001 |month=Oct |pmid=11546783 |doi=10.1074/jbc.M106831200 |url=http://www.jbc.org/cgi/content/full/276/43/39608] , it has no known signaling domainOMIM|600742|TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE III; TGFBR3] . It however may serve to enhance the binding of TGF beta ligands to TGF beta type II receptors by binding TGFβ and presenting it to TGFBR2. One of the downstream targets of TGF β signaling, "GIPC", binds to its PDZ domain, which prevents its proteosomal degradation, which subsequently increases TGFβ activity. It may also serve as an
inhibincoreceptor to ActivinRII.
BMP and Activin membrane bound inhibitor (BAMBI), has a similar extracellular domain as type I receptors. It lacks an intracellular serine/threonine protein kinase domain and hence is a pseudoreceptor. It binds to the type I receptor preventing it from being activated. It serves as a negative regulator of TGF beta signaling and may limit tgf-beta expression during embryogeneis. It requires BMP signaling for its expression
FKBP12 binds the GS region of the type I receptor preventing phosphorylation of the receptor by the type II receptors. It is believed that FKBP12 and its homologs help to prevent type I receptor activation in the absence of a ligands, since ligand binding causes its dissociation.
Role of inhibitory SMADs
There are two other SMADs which complete the SMAD family, the inhibitory SMADs (
I-SMADS), SMAD6and SMAD7. They play a key role in the regulation of TFG beta signaling and are involved in negative feeback. Like other SMADs they have an MH1 and an MH2 domain. SMAD7 competes with other R-SMADs with the Type I receptor and prevents their phosphorylationcite journal
author=Itoh F, Asao H, Sugamura K, Heldin CH, ten Dijke P, Itoh S |title=Promoting bone morphogenetic protein signaling through negative regulation of inhibitory Smads |journal=EMBO J. |volume=20 |issue=15 |pages=4132–42 |year=2001 |month=Aug |pmid=11483516 |pmc=149146 |doi=10.1093/emboj/20.15.4132 |url=] . It resides in the nucleus and upon TGF beta receptor activation translocates to the cytoplasm where it binds the type I receptor.
SMAD6binds SMAD4 preventing the binding of other R-SMADs with the coSMAD. The levels of I-SMAD increase with TGF beta signaling suggesting that they are downstream targets of TGF-beta signaling.
The E3 ubiquitin-protein
ligases SMURF1and SMURF2regulate the levels of SMADs. They accept ubiquitinfrom a E2 conjugating enzyme where they transfer ubiquitin to the RSMADs which causes their ubiquitination and subsequent proteosomal degradation. SMURF1 binds to SMAD1and SMAD5while SMURF2 binds SMAD1, SMAD2, SMAD3, SMAD6and SMAD7. It enhances the inhibitory action of SMAD7 while reducing the transcriptional activities of SMAD2.
*Kyoto Encyclopedia of Genes and Genomes - [http://www.genome.ad.jp/dbget-bin/show_pathway?hsa04350+7040 TGF beta signaling pathway] map
Wikimedia Foundation. 2010.
Look at other dictionaries:
TGF beta receptor 2 — Transforming growth factor, beta receptor II (70/80kDa) PDB rendering based on 1ktz … Wikipedia
TGF beta — Transforming growth factor beta (TGF β) controls proliferation, cellular differentiation, and other functions in most cells. It plays a role in immunity, cancer, heart disease and Marfan syndrome.Some cells secrete TGF β, and also have receptors… … Wikipedia
TGF-beta 1 — Factor de crecimiento transformante beta 1 Estructura tridimensional de la proteína TGF β1. HUGO … Wikipedia Español
Notch signaling pathway — Structure of the ligand binding region of the human NOTCH 1 receptor … Wikipedia
Signaling molecule — A signaling molecule is a chemical involved in transmitting information between cells. Such molecules are released from the cell sending the signal, cross over the gap between cells by diffusion, and interact with specific receptors in another… … Wikipedia
Cell signaling — is part of a complex system of communication that governs basic cellular activities and coordinates cell actions. [Witzany, G. (2000). Life: The Communicative Structure. Norderstedt, Libri BoD.] The ability of cells to perceive and correctly… … Wikipedia
Nodal signaling — is a signal transduction pathway that is important in pattern formation and differentiation during embryo development. The nodal family of proteins, a subset of the transforming growth factor beta (TGFβ) superfamily, is responsible for… … Wikipedia
Interleukin 8 receptor, beta — Chemokine (C X C motif) receptor 2 Identifiers Symbols CXCR2; CD182; CDw128b; CMKAR2; IL8R2; IL8RA; IL8RB External IDs … Wikipedia
Epoetin beta — Erythropoetin Oberflächenmodell von Erythropoetin (Mitte) im Komplex mit seinem Rezeptor, nach PDB … Deutsch Wikipedia
Mothers against decapentaplegic homolog 2 — SMAD family member 2 PDB rendering based on 1dev … Wikipedia