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Search results 1101 to 1147 out of 1147 for Notch3

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Type Details Score
Protein Domain
Type: Family
Description: This family includes the neurogenic mastermind-like proteins 1-3 (MAML1-3) from chordates, which act as critical transcriptional co-activators for Notch signaling [, ]. Notch receptors are cleaved upon ligand engagement and the intracellular domain of Notch shuttles to the nucleus. MAMLs form a functional DNA-binding complex with the cleaved Notch receptor and the transcription factor CSL, thereby regulating transcriptional events that are specific to the Notch pathway. MAML proteins may also play roles as key transcriptional co-activators in other signal transduction pathways as well, including: muscle differentiation and myopathies (MEF2C) [], tumour suppressor pathway (p53) []and colon carcinoma survival (beta-catenin) []. MAML proteins could mediate cross-talk among the various signaling pathways and the diverse activities of the MAML proteins converge to impact normal biological processes and human diseases, including cancers.They consist of an N-terminal domain which adopt an elongated kinked helix that wraps around ANK and CSL forming one of the complexes in the build-up of the Notch transcriptional complex for recruiting general transcription factors [, ]]. This N-terminal domain is responsible for its interaction with the ankyrin repeat region of the Notch proteins NOTCH1 [], NOTCH2 [], NOTCH3 []and NOTCH4. It forms a DNA-binding complex with Notch proteins and RBPSUH/RBP-J kappa/CBF1, and also binds CREBBP/CBP []and CDK8 []. The C-terminal region is required for transcriptional activation.
Protein Domain
Type: Domain
Description: This entry represents the N-terminal domain found in a family of neurogenic mastermind-like proteins (MAMLs), which act as critical transcriptional co-activators for Notch signaling [, , ]. Notch receptors are cleaved upon ligand engagement and the intracellular domain of Notch shuttles to the nucleus. MAMLs form a functional DNA-binding complex with the cleaved Notch receptor and the transcription factor CSL, thereby regulating transcriptional events that are specific to the Notch pathway. MAML proteins may also play roles as key transcriptional co-activators in other signal transduction pathways as well, including: muscle differentiation and myopathies (MEF2C) [], tumour suppressor pathway (p53) []and colon carcinoma survival (beta-catenin) []. MAML proteins could mediate cross-talk among the various signaling pathways and the diverse activities of the MAML proteins converge to impact normal biological processes and human diseases, including cancers.The N-terminal domain of MAML proteins adopt an elongated kinked helix that wraps around ANK and CSL forming one of the complexes in the build-up of the Notch transcriptional complex for recruiting general transcription factors []. This N-terminal domain is responsible for its interaction with the ankyrin repeat region of the Notch proteins NOTCH1 [], NOTCH2 [], NOTCH3 []and NOTCH4. It forms a DNA-binding complex with Notch proteins and RBPSUH/RBP-J kappa/CBF1, and also binds CREBBP/CBP []and CDK8 []. The C-terminal region is required for transcriptional activation.
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein
Organism: Mus musculus/domesticus
Length: 1210  
Fragment?: false
Publication  
First Author: Dabertrand F
Year: 2021
Journal: Proc Natl Acad Sci U S A
Title: PIP2 corrects cerebral blood flow deficits in small vessel disease by rescuing capillary Kir2.1 activity.
Volume: 118
Issue: 17
Publication  
First Author: Oka F
Year: 2022
Journal: J Clin Invest
Title: CADASIL mutations sensitize the brain to ischemia via spreading depolarizations and abnormal extracellular potassium homeostasis.
Volume: 132
Issue: 8
Genotype
Symbol: Gt(ROSA)26Sor/Gt(ROSA)26Sor Notch3/Notch3<+>
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac
Zygosity: cn
Has Mutant Allele: true
Publication
First Author: Huang S
Year: 2018
Journal: PLoS Biol
Title: Jagged1/Notch2 controls kidney fibrosis via Tfam-mediated metabolic reprogramming.
Volume: 16
Issue: 9
Pages: e2005233
Publication
First Author: Sullivan JP
Year: 2010
Journal: Cancer Res
Title: Aldehyde dehydrogenase activity selects for lung adenocarcinoma stem cells dependent on notch signaling.
Volume: 70
Issue: 23
Pages: 9937-48
Publication
First Author: Pradeep CR
Year: 2012
Journal: Oncogene
Title: Modeling ductal carcinoma in situ: a HER2-Notch3 collaboration enables luminal filling.
Volume: 31
Issue: 7
Pages: 907-17
Publication  
First Author: Sugiura K
Year: 2023
Journal: JCI Insight
Title: LIN28B promotes cell invasion and colorectal cancer metastasis via CLDN1 and NOTCH3.
Volume: 8
Issue: 14
Publication
First Author: Van de Walle I
Year: 2013
Journal: J Exp Med
Title: Specific Notch receptor-ligand interactions control human TCR-αβ/γδ development by inducing differential Notch signal strength.
Volume: 210
Issue: 4
Pages: 683-97
Publication
First Author: Osanyingbemi-Obidi J
Year: 2011
Journal: Mol Cancer Res
Title: Notch signaling contributes to lung cancer clonogenic capacity in vitro but may be circumvented in tumorigenesis in vivo.
Volume: 9
Issue: 12
Pages: 1746-54
Publication
First Author: Wang S
Year: 2017
Journal: J Cell Mol Med
Title: Ablation of endothelial prolyl hydroxylase domain protein-2 promotes renal vascular remodelling and fibrosis in mice.
Volume: 21
Issue: 9
Pages: 1967-1978
Publication
First Author: Wang S
Year: 2016
Journal: Oncotarget
Title: Loss of prolyl hydroxylase domain protein 2 in vascular endothelium increases pericyte coverage and promotes pulmonary arterial remodeling.
Volume: 7
Issue: 37
Pages: 58848-58861
Publication
First Author: Gopisetty A
Year: 2013
Journal: J Immunol
Title: OX40L/Jagged1 cosignaling by GM-CSF-induced bone marrow-derived dendritic cells is required for the expansion of functional regulatory T cells.
Volume: 190
Issue: 11
Pages: 5516-25
Publication
First Author: Klose R
Year: 2019
Journal: Sci Rep
Title: Loss of the serine protease HTRA1 impairs smooth muscle cells maturation.
Volume: 9
Issue: 1
Pages: 18224
Publication  
First Author: Zeng H
Year: 2016
Journal: Sci Rep
Title: LPS causes pericyte loss and microvascular dysfunction via disruption of Sirt3/angiopoietins/Tie-2 and HIF-2α/Notch3 pathways.
Volume: 6
Pages: 20931
Publication
First Author: Cuervo H
Year: 2017
Journal: Angiogenesis
Title: PDGFRβ-P2A-CreERT2 mice: a genetic tool to target pericytes in angiogenesis.
Volume: 20
Issue: 4
Pages: 655-662
Publication  
First Author: Papadakos KS
Year: 2019
Journal: Matrix Biol
Title: Cartilage Oligomeric Matrix Protein initiates cancer stem cells through activation of Jagged1-Notch3 signaling.
Volume: 81
Pages: 107-121
Publication
First Author: Kumar P
Year: 2019
Journal: J Immunol
Title: OX40L-JAG1-Induced Expansion of Lineage-Stable Regulatory T Cells Involves Noncanonical NF-κB Signaling.
Volume: 203
Issue: 12
Pages: 3225-3236
Publication
First Author: Li X
Year: 2023
Journal: FASEB J
Title: Deficiency of thrombospondin-2 alleviates intimal hyperplasia in mice by modulating vascular smooth muscle cell proliferation and migration.
Volume: 37
Issue: 2
Pages: e22743
Publication
First Author: Dudley DD
Year: 2009
Journal: PLoS One
Title: Hes1 potentiates T cell lymphomagenesis by up-regulating a subset of notch target genes.
Volume: 4
Issue: 8
Pages: e6678
Publication
First Author: Bargo S
Year: 2010
Journal: Biochem Biophys Res Commun
Title: Transforming acidic coiled-coil protein-3 (Tacc3) acts as a negative regulator of Notch signaling through binding to CDC10/Ankyrin repeats.
Volume: 400
Issue: 4
Pages: 606-12
Publication
First Author: Zhang C
Year: 2018
Journal: Cardiovasc Res
Title: Cbx3 inhibits vascular smooth muscle cell proliferation, migration, and neointima formation.
Volume: 114
Issue: 3
Pages: 443-455
Protein Domain
Type: Family
Description: Notch cell surface receptors are large, single-pass type-1 transmembrane proteins found in a diverse range of metazoan species, from human to Caenorhabditis species. The fruit fly, Drosophila melanogaster, possesses only one Notch protein, whereas in C.elegans, two receptors have been found; by contrast, four Notch paralogues (designated N1-4) have been identified in mammals, playing both unique and redundant roles. The hetero-oligomer Notch comprises a large extracellular domain (ECD), containing 10-36 tandem Epidermal Growth Factor (EFG)-like repeats, which are involved in ligand interactions; a negative regulatory region, including three cysteine-rich Lin12-Notch Repeats (LNR); a single trans-membrane domain (TM); a small intracellular domain (ICD), which includes a RAM (RBPjk-association module) domain; six ankyrin repeats (ANK), which are involved in protein-protein interactions; and a PEST domain. Drosophila Notch also contains an OPA domain []. Notch signalling is an evolutionarily conserved pathway involved in a wide variety of developmental processes, including adult homeostasis and stem cell maintenance, cell proliferation and apoptosis []. Notch is activated by a range of ligands -the so-called DSL ligands (Delta/Seratte/LAG-2). Activation is also mediated by a sequence of proteolytic events: ligand binding leads to cleavage of Notch by ADAM proteases []at site 2 (S2) and presenilin-1/g-secretase at sites 3 (S3)and 4 (S4) [].The last cleavage releases the Notch intracellular part of the protein (NICD) from the membrane and, upon release, the NICD translocates to the nucleus where it associates with a CBF1/RBJk/Su(H)/Lag1 (CSL) family of DNA-binding proteins. The subsequent recruitment of a co-activator mastermind like (MAML1) protein []promotes transcriptional activation of Notch target genes: well established Notch targets are the Hes and Hey gene families. Aberrant Notch function and signalling has been associated with a number of human disorders, including Allagile syndrome, spondylocostal dysostosis, aortic valve disease, CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy), and T-cell Acute Lympho-blastic Leukemia (T-ALL); it has also been implicated in various human carcinomas [, ]. Notch3 displays a more restrictive distribution than the rest of the Notch subtypes, being expressed predominantly in vascular smooth muscle cells, the central nervous system, certain thymocytes subsets, and in regulatory T cells [].
Publication
First Author: Zhang S
Year: 2016
Journal: Oncogene
Title: Lunatic Fringe is a potent tumor suppressor in Kras-initiated pancreatic cancer.
Volume: 35
Issue: 19
Pages: 2485-95
Publication  
First Author: Breikaa RM
Year: 2022
Journal: Vascul Pharmacol
Title: Loss of Jagged1 in mature endothelial cells causes vascular dysfunction with alterations in smooth muscle phenotypes.
Volume: 145
Pages: 107087
Publication
First Author: Li L
Year: 2013
Journal: PLoS One
Title: Myocardial injection of apelin-overexpressing bone marrow cells improves cardiac repair via upregulation of Sirt3 after myocardial infarction.
Volume: 8
Issue: 9
Pages: e71041
Publication
First Author: Kunze B
Year: 2020
Journal: Gastroenterology
Title: Notch Signaling Mediates Differentiation in Barrett's Esophagus and Promotes Progression to Adenocarcinoma.
Volume: 159
Issue: 2
Pages: 575-590
Publication
First Author: Alexander GM
Year: 2022
Journal: PLoS One
Title: Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.
Volume: 17
Issue: 9
Pages: e0274615
Publication
First Author: Andersson ER
Year: 2018
Journal: Gastroenterology
Title: Mouse Model of Alagille Syndrome and Mechanisms of Jagged1 Missense Mutations.
Volume: 154
Issue: 4
Pages: 1080-1095
Publication
First Author: Kopan R
Year: 2009
Journal: Cell
Title: The canonical Notch signaling pathway: unfolding the activation mechanism.
Volume: 137
Issue: 2
Pages: 216-33
Publication
First Author: Hartmann D
Year: 2002
Journal: Hum Mol Genet
Title: The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts.
Volume: 11
Issue: 21
Pages: 2615-24
Publication
First Author: Wu L
Year: 2000
Journal: Nat Genet
Title: MAML1, a human homologue of Drosophila mastermind, is a transcriptional co-activator for NOTCH receptors.
Volume: 26
Issue: 4
Pages: 484-9
Publication  
First Author: Gridley T
Year: 2003
Journal: Hum Mol Genet
Title: Notch signaling and inherited disease syndromes.
Volume: 12 Spec No 1
Pages: R9-13
Publication
First Author: Louvi A
Year: 2006
Journal: Nat Rev Neurosci
Title: Notch signalling in vertebrate neural development.
Volume: 7
Issue: 2
Pages: 93-102
Publication
First Author: De Strooper B
Year: 1999
Journal: Nature
Title: A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain.
Volume: 398
Issue: 6727
Pages: 518-22
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein
Organism: Mus musculus/domesticus
Length: 128  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 734  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 156  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 305  
Fragment?: false
Publication
First Author: Artavanis-Tsakonas S
Year: 1999
Journal: Science
Title: Notch signaling: cell fate control and signal integration in development.
Volume: 284
Issue: 5415
Pages: 770-6