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The expression patterns of contactin-2 at different time points after spinal cord injury were studied at the mRNA level.
two guidance cues, TAG-1 and laminin-alpha1, influence the behavior of growth cones during axon pathfinding in vivo
tag1, lama1 (zeige LAMA1 Proteine) and vangl2 (zeige VANGL2 Proteine) participate in a common mechanism that integrates signaling between the FBMN and its environment to regulate migration.
We further demonstrate that Cre expression initiates after birth with preservation of native Cntn2 protein. Finally, we show that Cntn23'UTR-IRES-Cre-EGFP/+ mice maintain normal cardiac mechanical and electrical function.
Tag1 is crucial for the olfactory circuit formation in mice.
Interaction proteomics revealed the interactors of Caspr2 (zeige CNTNAP2 Proteine), including CNTN2, KCNAs, members of the ADAM family (ADAM22 (zeige ADAM22 Proteine), ADAM23 (zeige Adam23 Proteine) and ADAM11 (zeige ADAM11 Proteine)), members of LGI family and MAGUKs (DLGs and MPPs (zeige MPHOSPH6 Proteine)).
Our results clearly demonstrate that mouse and human contactin-2 are physiological substrates for BACE1 (zeige BACE Proteine)
the TAG-1-mediated cell-to-cell interaction between the unpolarized multipolar cells and the pioneering axons regulates the polarization of multipolar cells partly through Lyn kinase and Rac1
This study demonistrated that knockdown of the cell-surface molecule TAG-1 resulted in retraction of neocortical progenitors' basal processes.
These results suggest that the Tax-induced decline in p53 (zeige TP53 Proteine) function, which is independent of NF-kappaB (zeige NFKB1 Proteine) activation in the early stage, might be the first stage in the onset of ATLL.
two novel genes, Cntnap2 (zeige CNTNAP2 Proteine) and Tag1, are implicated in the regulation of diet-induced obesity.
These observations identify a novel role for TAG1 in modulating the intracellular sorting of signaling receptor complexes.
These findings are consistent with a regulatory role for Tag-1 in axon emergence as well as migratory behavior by developing mouse cerebellar granule neurons.
the ectodomains of CNTNAP2 (zeige CNTNAP2 Proteine) and contactin 2 (CNTN2) bind directly and specifically, with low nanomolar affinity.
RACK1 (zeige GNB2L1 Proteine) interacts with CNTN2, and the effects of RACK1 (zeige GNB2L1 Proteine) on glioma cell growth and differentiation are mediated by CNTN2.
A single nucleotide deletion in exon 6 of CNTN2 results in a frameshift mutation, segregating in a recessive manner in a consanguineous Egyptian family with epilepsy.
allelic variation in TAG-1 does not play a major role in determining multifocal motor neuropathy susceptibility.
single nucleotide polymorphisms in TAG-1 are related to the IVIg responsiveness of Chronic inflammatory demyelinating polyneuropathy patients.
The domains responsible for the neurite outgrowth promoting activity of TAG-1 have been investigated as well as its interactions with other cell adhesion molecules.
TAG-1 homophilic interaction is based on dimer formation rather than formation of a molecular zipper as proposed for the chicken ortholog.
Contactin-2 is expressed by various neuronal populations and sequestered in the juxtaparanodal domain of myelinated axons both at the axonal and myelin sides; is an autoantigen targeted by T cells and autoantibodies in MS.
immune response to CNTN2 and possible involvement in multiple sclerosis and EAE [REVIEW]
The protein encoded by this gene is a member of the immunoglobulin superfamily. It is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. It may also be involved in glial tumorigenesis and may provide a potential target for therapeutic intervention.
, transiently expressed axonal glycoprotein
, contactin 2 (axonal)
, axonal glycoprotein TAG-1
, transient axonal glycoprotein 1
, transiently-expressed axonal glycoprotein
, axonin-1 cell adhesion molecule
, contactin 2 (transiently expressed)