Signaling by NOTCH4 (Homo sapiens)
From WikiPathways
Description
Similar to NOTCH1, NOTCH4 is activated by delta-like and jagged ligands (DLL/JAG) expressed in trans on a neighboring cell. The activation triggers cleavage of NOTCH4, first by ADAM10 at the S2 cleavage site, then by gamma-secretase at the S3 cleavage site, resulting in the release of the intracellular domain of NOTCH4, NICD4, into the cytosol. NICD4 subsequently traffics to the nucleus where it acts as a transcriptional regulator.
Original Pathway at Reactome: http://www.reactome.org/PathwayBrowser/#DB=gk_current&FOCUS_SPECIES_ID=48887&FOCUS_PATHWAY_ID=1980150
Quality Tags
Ontology Terms
Bibliography
View all... |
- Raafat A, Bargo S, McCurdy D, Callahan R.; ''The ANK repeats of Notch-4/Int3 activate NF-κB canonical pathway in the absence of Rbpj and causes mammary tumorigenesis.''; PubMed Europe PMC Scholia
- Shawber CJ, Funahashi Y, Francisco E, Vorontchikhina M, Kitamura Y, Stowell SA, Borisenko V, Feirt N, Podgrabinska S, Shiraishi K, Chawengsaksophak K, Rossant J, Accili D, Skobe M, Kitajewski J.; ''Notch alters VEGF responsiveness in human and murine endothelial cells by direct regulation of VEGFR-3 expression.''; PubMed Europe PMC Scholia
- Bargo S, Raafat A, McCurdy D, Amirjazil I, Shu Y, Traicoff J, Plant J, Vonderhaar BK, Callahan R.; ''Transforming acidic coiled-coil protein-3 (Tacc3) acts as a negative regulator of Notch signaling through binding to CDC10/Ankyrin repeats.''; PubMed Europe PMC Scholia
- Raafat A, Bargo S, Anver MR, Callahan R.; ''Mammary development and tumorigenesis in mice expressing a truncated human Notch4/Int3 intracellular domain (h-Int3sh).''; PubMed Europe PMC Scholia
- Raafat A, Zoltan-Jones A, Strizzi L, Bargo S, Kimura K, Salomon D, Callahan R.; ''Kit and PDGFR-alpha activities are necessary for Notch4/Int3-induced tumorigenesis.''; PubMed Europe PMC Scholia
- Qian C, Liu F, Ye B, Zhang X, Liang Y, Yao J.; ''Notch4 promotes gastric cancer growth through activation of Wnt1/β-catenin signaling.''; PubMed Europe PMC Scholia
- Tang Y, Urs S, Liaw L.; ''Hairy-related transcription factors inhibit Notch-induced smooth muscle alpha-actin expression by interfering with Notch intracellular domain/CBF-1 complex interaction with the CBF-1-binding site.''; PubMed Europe PMC Scholia
- James AC, Szot JO, Iyer K, Major JA, Pursglove SE, Chapman G, Dunwoodie SL.; ''Notch4 reveals a novel mechanism regulating Notch signal transduction.''; PubMed Europe PMC Scholia
- Kusano S, Raab-Traub N.; ''An Epstein-Barr virus protein interacts with Notch.''; PubMed Europe PMC Scholia
- Fukusumi T, Guo TW, Sakai A, Ando M, Ren S, Haft S, Liu C, Amornphimoltham P, Gutkind JS, Califano JA.; ''The NOTCH4-HEY1 Pathway Induces Epithelial-Mesenchymal Transition in Head and Neck Squamous Cell Carcinoma.''; PubMed Europe PMC Scholia
- Li Y, Wu S, Pu J, Huang X, Zhang P.; ''Dengue virus up-regulates expression of notch ligands Dll1 and Dll4 through interferon-β signalling pathway.''; PubMed Europe PMC Scholia
- Uyttendaele H, Marazzi G, Wu G, Yan Q, Sassoon D, Kitajewski J.; ''Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene.''; PubMed Europe PMC Scholia
- Welcker M, Clurman BE.; ''FBW7 ubiquitin ligase: a tumour suppressor at the crossroads of cell division, growth and differentiation.''; PubMed Europe PMC Scholia
- Bonyadi Rad E, Hammerlindl H, Wels C, Popper U, Ravindran Menon D, Breiteneder H, Kitzwoegerer M, Hafner C, Herlyn M, Bergler H, Schaider H.; ''Notch4 Signaling Induces a Mesenchymal-Epithelial-like Transition in Melanoma Cells to Suppress Malignant Behaviors.''; PubMed Europe PMC Scholia
- Aste-Amézaga M, Zhang N, Lineberger JE, Arnold BA, Toner TJ, Gu M, Huang L, Vitelli S, Vo KT, Haytko P, Zhao JZ, Baleydier F, L'Heureux S, Wang H, Gordon WR, Thoryk E, Andrawes MB, Tiyanont K, Stegmaier K, Roti G, Ross KN, Franlin LL, Wang H, Wang F, Chastain M, Bett AJ, Audoly LP, Aster JC, Blacklow SC, Huber HE.; ''Characterization of Notch1 antibodies that inhibit signaling of both normal and mutated Notch1 receptors.''; PubMed Europe PMC Scholia
- MacKenzie F, Duriez P, Wong F, Noseda M, Karsan A.; ''Notch4 inhibits endothelial apoptosis via RBP-Jkappa-dependent and -independent pathways.''; PubMed Europe PMC Scholia
- Shawber CJ, Das I, Francisco E, Kitajewski J.; ''Notch signaling in primary endothelial cells.''; PubMed Europe PMC Scholia
- Das I, Craig C, Funahashi Y, Jung KM, Kim TW, Byers R, Weng AP, Kutok JL, Aster JC, Kitajewski J.; ''Notch oncoproteins depend on gamma-secretase/presenilin activity for processing and function.''; PubMed Europe PMC Scholia
- Wu G, Lyapina S, Das I, Li J, Gurney M, Pauley A, Chui I, Deshaies RJ, Kitajewski J.; ''SEL-10 is an inhibitor of notch signaling that targets notch for ubiquitin-mediated protein degradation.''; PubMed Europe PMC Scholia
- Ramakrishnan G, Davaakhuu G, Chung WC, Zhu H, Rana A, Filipovic A, Green AR, Atfi A, Pannuti A, Miele L, Tzivion G.; ''AKT and 14-3-3 regulate Notch4 nuclear localization.''; PubMed Europe PMC Scholia
- Tsunematsu R, Nakayama K, Oike Y, Nishiyama M, Ishida N, Hatakeyama S, Bessho Y, Kageyama R, Suda T, Nakayama KI.; ''Mouse Fbw7/Sel-10/Cdc4 is required for notch degradation during vascular development.''; PubMed Europe PMC Scholia
- Gallahan D, Callahan R.; ''Mammary tumorigenesis in feral mice: identification of a new int locus in mouse mammary tumor virus (Czech II)-induced mammary tumors.''; PubMed Europe PMC Scholia
- Strohmaier H, Spruck CH, Kaiser P, Won KA, Sangfelt O, Reed SI.; ''Human F-box protein hCdc4 targets cyclin E for proteolysis and is mutated in a breast cancer cell line.''; PubMed Europe PMC Scholia
- Lai PY, Tsai CB, Tseng MJ.; ''Active form Notch4 promotes the proliferation and differentiation of 3T3-L1 preadipocytes.''; PubMed Europe PMC Scholia
- Saxena MT, Schroeter EH, Mumm JS, Kopan R.; ''Murine notch homologs (N1-4) undergo presenilin-dependent proteolysis.''; PubMed Europe PMC Scholia
- Simões BM, O'Brien CS, Eyre R, Silva A, Yu L, Sarmiento-Castro A, Alférez DG, Spence K, Santiago-Gómez A, Chemi F, Acar A, Gandhi A, Howell A, Brennan K, Rydén L, Catalano S, Andó S, Gee J, Ucar A, Sims AH, Marangoni E, Farnie G, Landberg G, Howell SJ, Clarke RB.; ''Anti-estrogen Resistance in Human Breast Tumors Is Driven by JAG1-NOTCH4-Dependent Cancer Stem Cell Activity.''; PubMed Europe PMC Scholia
- Robbins J, Blondel BJ, Gallahan D, Callahan R.; ''Mouse mammary tumor gene int-3: a member of the notch gene family transforms mammary epithelial cells.''; PubMed Europe PMC Scholia
- Uyttendaele H, Ho J, Rossant J, Kitajewski J.; ''Vascular patterning defects associated with expression of activated Notch4 in embryonic endothelium.''; PubMed Europe PMC Scholia
- Andersson ER, Lendahl U.; ''Therapeutic modulation of Notch signalling--are we there yet?''; PubMed Europe PMC Scholia
- Raafat A, Lawson S, Bargo S, Klauzinska M, Strizzi L, Goldhar AS, Buono K, Salomon D, Vonderhaar BK, Callahan R.; ''Rbpj conditional knockout reveals distinct functions of Notch4/Int3 in mammary gland development and tumorigenesis.''; PubMed Europe PMC Scholia
- Wei SJ, Williams JG, Dang H, Darden TA, Betz BL, Humble MM, Chang FM, Trempus CS, Johnson K, Cannon RE, Tennant RW.; ''Identification of a specific motif of the DSS1 protein required for proteasome interaction and p53 protein degradation.''; PubMed Europe PMC Scholia
- Lin SE, Oyama T, Nagase T, Harigaya K, Kitagawa M.; ''Identification of new human mastermind proteins defines a family that consists of positive regulators for notch signaling.''; PubMed Europe PMC Scholia
- Voges D, Zwickl P, Baumeister W.; ''The 26S proteasome: a molecular machine designed for controlled proteolysis.''; PubMed Europe PMC Scholia
History
View all... |
External references
DataNodes
View all... |
Name | Type | Database reference | Comment |
---|---|---|---|
12xFucT-11xGlcS-6xFucS-NOTCH4 | Protein | Q99466 (Uniprot-TrEMBL) | |
ADAM10 Zn++ | Complex | REACT_3937 (Reactome) | |
ADAM10 | Protein | O14672 (Uniprot-TrEMBL) | |
APH1A | Protein | Q96BI3 (Uniprot-TrEMBL) | |
APH1B | Protein | Q8WW43 (Uniprot-TrEMBL) | |
DLL/JAG NOTCH4 | Complex | REACT_2938 (Reactome) | |
DLL/JAG | Protein | REACT_5356 (Reactome) | |
DLL1 | Protein | O00548 (Uniprot-TrEMBL) | |
DLL4 | Protein | Q9NR61 (Uniprot-TrEMBL) | |
JAG1 | Protein | P78504 (Uniprot-TrEMBL) | |
JAG2 | Protein | Q9Y219 (Uniprot-TrEMBL) | |
NCSTN | Protein | Q92542 (Uniprot-TrEMBL) | |
NICD4 | Protein | Q99466 (Uniprot-TrEMBL) | |
NOTCH4 fragment DLL/JAG | Complex | REACT_5162 (Reactome) | |
NOTCH4 | Protein | Q99466 (Uniprot-TrEMBL) | |
NOTCH4 | Complex | REACT_3481 (Reactome) | |
PSEN2 | Protein | P49810 (Uniprot-TrEMBL) | |
PSENEN | Protein | Q9NZ42 (Uniprot-TrEMBL) | |
Pre-NOTCH Expression and Processing | Pathway | REACT_118744 (Reactome) | In humans and other mammals the NOTCH gene family has four members, NOTCH1, NOTCH2, NOTCH3 and NOTCH4, encoded on four different chromosomes. Their transcription is developmentally regulated and tissue specific, but very little information exists on molecular mechanisms of transcriptional regulation. Translation of NOTCH mRNAs is negatively regulated by a number of recently discovered microRNAs (Li et al. 2009, Pang et al.2010, Ji et al. 2009, Kong et al. 2010, Marcet et al. 2011, Ghisi et al. 2011, Song et al. 2009, Hashimoto et al. 2010, Costa et al. 2009). The nascent forms of NOTCH precursors, Pre-NOTCH1, Pre-NOTCH2, Pre-NOTCH3 and Pre-NOTCH4, undergo extensive posttranslational modifications in the endoplasmic reticulum and Golgi apparatus to become functional. In the endoplasmic reticulum, conserved serine and threonine residues in the EGF repeats of NOTCH extracellular domain are fucosylated and glucosylated by POFUT1 and POGLUT1, respectively (Yao et al. 2011, Stahl et al. 2008, Wang et al. 2001, Shao et al. 2003, Acar et al. 2008, Fernandez Valdivia et al. 2011). In the Golgi apparatus, fucose groups attached to NOTCH EGF repeats can be elongated by additional glycosylation steps initiated by fringe enzymes (Bruckner et al. 2000, Moloney et al. 2000, Cohen et al. 1997, Johnston et al. 1997, Chen et al. 2001). Fringe-mediated modification modulates NOTCH signaling but is not an obligatory step in Pre-NOTCH processing. Typically, processing of Pre-NOTCH in the Golgi involves cleavage by FURIN convertase (Blaumueller et al. 1997, Logeat et al. 1998, Gordon et al. 2009, Rand et al. 2000, Chan et al. 1998). The cleavage of NOTCH results in formation of mature NOTCH heterodimers that consist of NOTCH extracellular domain (NEC i.e. NECD) and NOTCH transmembrane and intracellular domain (NTM i.e. NTMICD). NOTCH heterodimers translocate to the cell surface where they function in cell to cell signaling. |
Zn2+ | Metabolite | CHEBI:29105 (ChEBI) | |
gamma-secretase complex | Complex | REACT_5292 (Reactome) |
Annotated Interactions
View all... |
Source | Target | Type | Database reference | Comment |
---|---|---|---|---|
ADAM10 Zn++ | mim-catalysis | REACT_1011 (Reactome) | ||
DLL/JAG | REACT_1381 (Reactome) | |||
NICD4 | Arrow | REACT_965 (Reactome) | ||
NOTCH4 fragment DLL/JAG | Arrow | REACT_1011 (Reactome) | ||
NOTCH4 | Arrow | REACT_1011 (Reactome) | ||
NOTCH4 | Arrow | REACT_965 (Reactome) | ||
NOTCH4 | REACT_1381 (Reactome) | |||
REACT_1011 (Reactome) | Ligand binding induces a conformational change in the NOTCH4, probably through mechanical pulling of NOTCH4 triggered by endocytosis of receptor-attached ligand. This conformational change exposes the S2 site in the extracellular region of NOTCH4 and results in cleavage of NOTCH4 by ADAM10 metalloprotease, generating the membrane-anchored NOTCH4 fragment NEXT4. The extracellular NOTCH4 portion remains attached to the ligand presented on the plasma membrane of a neighboring cell. | |||
REACT_1381 (Reactome) | The NOTCH4 receptor is activated by binding a Delta-like (DLL) or Jagged (JAG) ligand presented on the plasma membrane of a neighbouring cell. | |||
REACT_857 (Reactome) | The cytosolic NICD4 translocates to the nucleus. | |||
REACT_965 (Reactome) | NEXT4 fragment of NOTCH4 is further cleaved at the S3 site by the gamma-secretase complex, which relases the intracellular domain NICD4 into the cytosol. | |||
gamma-secretase complex | mim-catalysis | REACT_965 (Reactome) |