|
ORF cDNA clones
|
CRISPR / TALEN
|
Lentivirus
|
AAV
|
TALE-TF
|
ORF knockin clones
|
|
Antibody
|
Proteins
|
miRNA target clones
|
qPCR primers
|
shRNA clones
|
miRNA products
|
Promoter clones
|
Validated All-in-One™ qPCR Primer for PVR(NM_006505.4) Search again
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Summary
The protein encoded by this gene is a transmembrane glycoprotein belonging to the immunoglobulin superfamily. The external domain mediates cell attachment to the extracellular matrix molecule vitronectin, while its intracellular domain interacts with the dynein light chain Tctex-1/DYNLT1. The gene is specific to the primate lineage, and serves as a cellular receptor for poliovirus in the first step of poliovirus replication.
Gene References into function
- We propose that the cytoplasmic domain may target CD155-containing endocytic vesicles to the microtubular network
- activation of expression of sonic hedgehog protein
- Data show that both PVR and Nectin-2 represent specific ligands for the DNAM-1 triggering receptor.
- CD155 may have an important role in cellular function
- These data indicate that Tage4 represents the functional orthologue of CD155 in mouse.
- that DNAM-1 regulates monocyte extravasation via its interaction with CD226 expressed at endothelial junctions on normal cells.
- These results suggest that CD155alpha plays a role in the regulation of cell adhesion and cell motility.
- cytoplasmic domain of PVR directly interacts with Tctex-1 and plays an important role in retrograde transport of poliovirus-containing vesicles along microtubules in vivo
- Upregulation of the molecular target CD155 renders explant cultures of high-grade malignant gliomas highly susceptible to a prototype oncolytic poliovirus recombinant.
- Analysis of the ligands for triggering NK receptors revealed the consistent expression of cd155 and cd112 in myeloid leukemias, and less frequent expression in lymphoblastic leukemias
- Evasion of NK cell killing was mediated by human cytomegalovirus UL141 blocking surface expression of CD155
- Necl-5 has a critical role in integrin alphavbeta3 clustering and focal complex formation
- Results describe the establishment of a poliovirus oral infection system in human poliovirus receptor-expressing transgenic mice that are deficient in alpha/beta interferon receptor.
- no statistically significant association between this marker allele and non-syndromic clefting
- CD155, at least in part, enhances the proliferation of ras-mutated cells
- crystal structure of C155 D1D2 has been determined to 3.5-A resolution and fitted into approximately 8.5-A resolution cryoelectron microscopy reconstructions of the virus-receptor complexes for the 3 PV serotypes
- CD96-driven adhesion to CD155 may be crucial in developmental processes
