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results demonstrate that PntP1 prevents both the premature differentiation and the dedifferentiation of INPs by regulating the expression of distinct target genes at different stages of imINP development.
Both PntP1 and PntP2 are required for oenocyte specification. Since PntP1 is a downstream effector of EGF (show EGFR ELISA Kits) signaling, these findings provide insight into how a Hox (show MSH2 ELISA Kits) factor can both trigger and potentiate the EGF (show EGFR ELISA Kits) signal to promote an essential cell fate along the body plan.
PntP2 transcription factor plays a role in air sac (show ADCY10 ELISA Kits) development by regulation of the EGF (show EGFR ELISA Kits) ligand Vein protein.
These studies identify Cic (show CIC ELISA Kits), Pnt, and Ets21C as critical downstream effectors of EGFR (show EGFR ELISA Kits) signaling in Drosophila Intestinal Stem Cells
Btd (show BTD ELISA Kits) prevents the premature differentiation by suppressing the expression of Prospero (show PROX1 ELISA Kits) in immature intermediate neural progenitor cells. Btd (show BTD ELISA Kits) functions cooperatively with Pointed P1 to promote the generation of the above cells.
instances of co-expressed Yan and Pnt-GFP in tissues with high RTK signaling cannot be explained by the current model, and thus they provide important contexts for future investigation of how context-specific differences in RTK signaling
Data show that Appl (show APP ELISA Kits) is directly regulated by the Ras/MAPK (show MAPK1 ELISA Kits) pathway through a mechanism mediated by PntP2.
Specific disruption of either pntP1 or pntP2 resulted in the same R8-only phenotype, demonstrating that both Pnt isoforms are essential for photoreceptor recruitment
a low level of Notch (show NOTCH1 ELISA Kits) signaling functions to maintain the neuroepithelial cell identity by suppressing the expression of pointedP1 gene through the transcriptional repressor Anterior open.
Demonstrate that the Pointed-P2 PNT domain contains a dynamic N-terminal helix H0 appended to a core conserved five-helix bundle diagnostic of the SAM (show TTN ELISA Kits) domain fold.
Homozygous deletion of Ets2 in p53 (show TP53 ELISA Kits) mutant mice resulted in strong down-regulation of snoRNAs and reversed the prometastatic phenotype of mutant p53 (show TP53 ELISA Kits) but had no effect on osteosarcoma development, which remained 100% penetrant.
These results suggest an unappreciated role for ETS2 in fibroblasts in establishing an immune-suppressive microenvironment in response to oncogenic Kras(G12D) signaling during the initial stages of tumor development.
The differentiation of ERF-overexpressing trophoblast stem cell lines also suggests that ERF may have an FGF2 (show FGF2 ELISA Kits)-independent effect during the commitment towards syncytiotrophoblasts.
MicroRNA 17-92 cluster mediates ETS1 and ETS2-dependent RAS-oncogenic transformation
Elf5 (show ELF5 ELISA Kits) and Ets2 have roles in maintaining the mouse extraembryonic ectoderm in a dosage dependent synergistic manner
identified Ets2 as a key novel regulator in both the positive and negative control of miR (show MLXIP ELISA Kits)-155 in the inflammatory response.
The data reveals a key function for Ets2 in tumor fibroblasts in signaling to endothelial cells to promote tumor angiogenesis.
Data indicate that differences between the N termini of transcription factors Ets1 (show ETS1 ELISA Kits) and Ets2, rather than differences in the DNA binding domains, determine whether the proteins are capable of blocking antibody-secreting cells (ASCs) formation or not.
propose a model that provides a genetic explanation as to how Ets2 in trophoblast mediates the progression of gastrulation within the epiblast
Ets-2 play a key role in transcriptional regulation of CTRP5 (show C1QTNF5 ELISA Kits) in muscle cells.
Interaction with ZMYND11 mediates opposing roles of Ras-responsive ETS1 (show ETS1 ELISA Kits) and ETS2.
Data suggest marked changes in DNA methylation (show HELLS ELISA Kits) occur at a single CpG site (CpG4) in promoter region of ESR1 (show ESR1 ELISA Kits) as breast cancer cells become resistant to hormonal/aromatase (show CYP19A1 ELISA Kits) inhibitor antineoplastic agents; this CpG region is completely conserved among species, suggesting that it acts as a methylation-sensitive ETS2 transcription factor binding site/response element. (ESR1 (show ESR1 ELISA Kits) = estrogen receptor 1 (show ESR1 ELISA Kits); ETS2 = ETS (show ETS1 ELISA Kits) proto-oncogene (show RAB1A ELISA Kits) 2)
ETS2 and Twist1 (show TWIST1 ELISA Kits) promote invasiveness of Helicobacter pylori-infected gastric cancer cells by inducing Siah2 (show SIAH2 ELISA Kits)
Neuronal C-ETS2 senses oxidative stress, activates TFEB transcription, and mediates the upregulation of lysosomal genes.
ETS2, HNF4A (show HNF4A ELISA Kits) and JUNB (show JUNB ELISA Kits) are synergistic master regulators of epithelial-to-mesenchymal transition in cancer.
ATO treatment upregulated Ets-2 and miR (show MLXIP ELISA Kits)-126 expression in HUVECs.
RNA-seq evidence of biallelic expression of ETS2 and 10 neighboring genes in at least one primary human tissue tested indicates that the expression of ETS2 is uncoupled from the control of the maternally inherited 5mCpG imprints at the WRB (show WRB ELISA Kits) differentially methylated region (DMR (show WDR20 ELISA Kits)) in disomic controls or trisomy (Down syndrome) individuals.
Data show that NF-kappa-B (show NFKB1 ELISA Kits) p52 (show FKBP4 ELISA Kits) subunit (p52 (show FKBP4 ELISA Kits)) interacts with ets (show ETS1 ELISA Kits) transcription factors ETS1 (show ETS1 ELISA Kits)/2 factors at the C250T telomerase (TERT (show TERT ELISA Kits)) promoter to mediate TERT (show TERT ELISA Kits) reactivation.
ETS-1 (show ETS1 ELISA Kits)/ETS-2 and C/EBPalpha (show CEBPA ELISA Kits) could interact with corresponding binding sites.
DLX3 has a central role in controlling IFNT gene expression by associating with ETS2 on the IFNT promoter.
This gene encodes a transcription factor which regulates genes involved in development and apoptosis. The encoded protein is also a protooncogene and shown to be involved in regulation of telomerase. A pseudogene of this gene is located on the X chromosome. Alternative splicing results in multiple transcript variants.
, Ets at 58AB
, Ets protein pointed P2
, no terminal cell clones-R
, pointed P2
, avian leukemia oncogene 2
, protein C-ets-2
, oncogene ETS-2
, v-ets avian erythroblastosis virus E2 oncogene homolog 2
, v-ets erythroblastosis virus E26 oncogene homolog 2
, E26 avian leukemia oncogene 2, 3' domain
, avian erythroblastosis virus E26 (v-ets) oncogene homolog 2
, v-ets avian erythroblastosis virus E26 oncogene homolog 2