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Human TFAP2A Protein expressed in Wheat germ - ABIN1322523
Zhang, Li, Shibahara, Takahashi: Synergistic activation of the human adrenomedullin gene promoter by Sp1 and AP-2alpha. in Peptides 2008
AP2a initiates neural border patterning and is sufficient to elicit a neural border-like pattern in neuralized (show NEURL Proteins) ectoderm.
Genetic interaction between tfap2a and mitfa suggest that the factors en (show MITF Proteins)coded by these genes regulate shared targets in melanocytes, possibly within single or converging pathways.
these data support a model in which Tfap2a, acting through Bmp7a (show BMP7 Proteins), modulates Fgf and Notch (show NOTCH1 Proteins) signaling to control the duration, amount and speed of SAG (show SAG Proteins) neural development.
Prdm1a directly binds and activates a tfap2a enhancer at the NPB
Low Bmp activates expression of the transcription factor Tfap2a as part of a gene regulatory network that coordinates development of neural crest, preplacodal ectoderm and individual placodes in zebrafish.
tfap2a and foxd3 (show FOXD3 Proteins) are expressed during gastrulation prior to neural crest induction in distinct, complementary, domains; tfap2a is expressed in the ventral non-neural ectoderm and foxd3 (show FOXD3 Proteins) in the dorsal mesendoderm and ectoderm
These results reveal that mutations in TFAP2A are associated with a wide range of eye phenotypes and that hypomorphic tfap2a mutations can increase the risk of developmental defects arising from mutations at other loci.
These findings reveal that Tfap2 activity, mediated redundantly by Tfap2a and Tfap2e (show TFAP2E Proteins), promotes melanophore differentiation in parallel with Mitf (show MITF Proteins) by an effector other than Kit.
Results demonstrate that tfap2a is required for early steps in neural crest development and for the survival of a subset of neural crest derivatives.
data show that hindbrain noradrenergic neurons of the locus coeruleus and the posterior groups both require Tfap2a to establish their noradrenergic identity
Ap-2alpha regulates multiple steps of melanophore development, and is required for development of other neuronal and non-neuronal neural crest derivatives.
We identified miR (show MLXIP Proteins)-1254 as a negative regulator inhibiting HO-1 (show HMOX1 Proteins) translation by directly targeting HO-1 (show HMOX1 Proteins) 3'UTR via its seed region, and suppressing HO-1 (show HMOX1 Proteins) transcription via non-seed region-dependent inhibition of transcriptional factor AP-2 alpha (TFAP2A), a transcriptional activator of HO-1 (show HMOX1 Proteins).
dimerization-defective mutant of Nef failed to interact with either CD4 (show CD4 Proteins) or AP-2 (show GTF3A Proteins) in the BiFC assay, indicating that Nef quaternary structure is required for CD4 (show CD4 Proteins) and AP-2 (show GTF3A Proteins) recruitment as well as CD4 (show CD4 Proteins) down-regulation
Data show that TFAP2A binds many of the same regulatory elements as MITF (show MITF Proteins) in melanocytes.
the atrial fibrillation (AF)-associated SNP rs2595104 altered PITX2c (show PITX2 Proteins) expression via interaction with TFAP2a; such a pathway could ultimately contribute to AF susceptibility at the PITX2 (show PITX2 Proteins) locus associated with AF
AP-2a is an important transcription factor of DEK (show DEK Proteins) expression, which is correlated with the methylation level of the DEK (show DEK Proteins) core promoter in hepatocellular carcinoma .
AP-2alpha expression has a role in human hepatocellular cancer by regulating signaling to affect cell growth and migration
Hepatitis B virus X protein is able to elevate the expression of SPHK1 (show SPHK1 Proteins) in hepatoma cells by upregulating transcription factor AP2 alpha.
Results indicate that AP-2alpha activates COX-2 expression to promote NPC (show NPC1 Proteins) growth.
The AP-2alpha transcription factor may play an important role in suppressing glioma progression.
TFAP2A might play a role in the development of Ovarian Cancer, and may be a therapeutic target in OC.
Study systematically examined the expression profile of AP-2 family in the developing mouse and chick spinal cord and found that AP-2alpha and AP-2beta (show TFAP2B Proteins) are specifically expressed in post-mitotic dorsal interneurons. Subsequent functional assessment in chick embryos demonstrated that AP-2alpha and AP-2beta (show TFAP2B Proteins) have distinct functions in dorsal interneuron specification and differentiation.
MEX3C (show MEX3C Proteins) associates with the endolysosomal compartment through an endocytosis-like process. siRNA-mediated inhibition of the MEX3C (show MEX3C Proteins) or AP-2 complex (show AP2B1 Proteins) substantially decreased exosomal but not cellular microRNA miR (show MLXIP Proteins)-451a expression
High AP-2 alpha phosphorylation is associated with abdominal aortic aneurysm.
overexpression of Dnmt3a (show DNMT3A Proteins) partially rescued the impairment of adipogenesis induced by AP2alpha knockdown.
TFAP2A is a conserved component of the core network that regulates EMT, acting as a repressor of many genes, including ZEB2.
The AP-2beta (show TFAP2B Proteins) transcription factor is an important effector of PITX2 (show PITX2 Proteins) function during corneal development, required for differentiation of corneal endothelium and establishment of angiogenic privilege.
the regulation of synaptic-vesicle (SV) recycling via early endosomes by the interdependent regulation of AP-2-mediated endocytosis and AP-1 (show JUN Proteins)/sigma1B (show AP1S2 Proteins)-mediated SV reformation, is reported.
By gain-of function and loss-of-function approaches, ap2a and 2b were identified to be the major downstream targets of Ptf1a (show PTF1A Proteins) to specify the amacrine cell fate.
Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 (show FGF8 Proteins) gene dosage
The protein encoded by this gene is a transcription factor that binds the consensus sequence 5'-GCCNNNGGC-3'. The encoded protein functions as either a homodimer or as a heterodimer with similar family members. This protein activates the transcription of some genes while inhibiting the transcription of others. Defects in this gene are a cause of branchiooculofacial syndrome (BOFS). Three transcript variants encoding different isoforms have been found for this gene.
transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
, transcription factor AP-2 alpha
, AP-2 transcription factor
, transcription factor AP-2-alpha
, transcription factor AP-2
, Transcription factor AP-2 alpha
, adipocyte lipid-binding protein
, adipocyte-type fatty acid-binding protein
, fatty acid-binding protein 4
, fatty acid-binding protein, adipocyte
, activating enhancer-binding protein 2 alpha
, activating enhancer-binding protein 2-alpha
, activator protein 2
, mont blanc
, AP-2 alpha
, Ap-2 (a)