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High OCT4 expression is associated with enhancement of angiogenesis in lung cancer.
Logistic regression analysis revealed that OCT4 rs1265163 showed the most significant association signal for the risk of chronic hepatitis B (CHB). Linkage disequilibrium and conditional analysis confirmed rs1265163 in OCT4 as a novel genetic marker for CHB susceptibility.
the pluripotency transcription factor OCT4 can serve as a metabolic-redox sensor in human embryonic stem cells and that metabolic cues can act in concert with growth factor signaling to orchestrate stem cell differentiation.
High OCT4 expression is associated with brain neoplasms.
Studies suggest that embryonic signaling pathways, the likes of Notch (show NOTCH1 ELISA Kits), Wnt (show WNT2 ELISA Kits), and Hedgehog (show SHH ELISA Kits) and tumor marker Oct-4 offer targets for cascade-specific molecular inhibition as they are fundamental to (cancer and normal) stem cell maintenance and growth.
The quadruplex acts as a strong, positive regulator of Oct4 expression.
these findings demonstrated that HIF-2alpha (show EPAS1 ELISA Kits) in vselMSCs cooperated with Oct4 in survival and function. The identification of the cooperation between HIF-2alpha (show EPAS1 ELISA Kits) and Oct4 will lead to deeper characterization of the downstream targets of this interaction in vselMSCs and will have novel pathophysiological implications for the repair of infarcted myocardium.
gene editing reveals a role for OCT4 in human embryogenesis
we are reporting a new variant of OCT4, which is expressed under different physiological conditions. The finding shed more light on complexity of OCT4 expression and functions.
High Oct4 expression is associated with breast cancer.
Cytoplasmic CD44 (show CD44 ELISA Kits) and absence of nuclear Oct3/4 suggest that the cells of cardiac sarcomas may represent 'daughter' stem cells that no longer have the capacity for tumour initiation, but have subsequently developed new lines of partial differentiation.
Lack of restricted OCT4 protein, and inner cell mass localization of NANOG in primate blastocysts, suggests that NANOG may determine inner cell mass fate more specifically during primate development.
The authors show, at single-cell resolution in vivo, that Pou5f3 complexes with Nanog to pattern mesendoderm differentiation at the blastula stage.
Data suggest that, in developing gastrula, Znfl1 controls developmental gene expression of Hoxb1b in embryonic posterior neuroectoderm by acting upstream of Pou5f3 and Sall4 (show SALL4 ELISA Kits); these proteins appear to be involved in neurogenesis. (Znfl1 = zinc finger-like gene 1; Hoxb1b = homeobox B1b protein; Pou5f3 = POU domain class 5 transcription factor 3 (show TCF3 ELISA Kits); Sall4 (show SALL4 ELISA Kits) = spalt (show SALL1 ELISA Kits)-like transcription factor 4 (show TCF4 ELISA Kits))
Regulation of mych by Pou5f1 appears to be direct transcriptional activation.
The posttranslational modification by phosphorylation opens the possibility that Pou5f1 may be subject to temporal or region specific modulation of its activity or stability by embryonic signaling mechanisms.
discuss mechanistic implications of simultaneous activation of transcriptional targets by ubiquitous, like Pou5f1, and region-specific inducers, emerging as a common regulatory motif in early development
maternal Nanog (show NANOG ELISA Kits), Pou5f1 and SoxB1 are required to initiate the zygotic developmental program and induce clearance of the maternal program by activating miR (show MYLIP ELISA Kits)-430 expression
thses data position Pou5f1 and SOX (show PIPOX ELISA Kits)-POU sites at the center of the zygotic gene activation network of vertebrates and provide a link between zygotic gene activation and pluripotency control.
The defects due to HEP induction were rescued by introducing wild-type pou2 mRNA before the heat treatments.
Vox plays a key role downstream of BMP signals in regulating the capacity of Nodal to induce endoderm versus mesoderm by modulating the activity of the Casanova/Pou2 regulatory system.
Pou2 functions in multiple aspects of vertebrate development, especially in the binary decision of the mesendoderm to mesoderm and endoderm in different ways depending on the developmental stage.
sequences of mRNA and translated protein of the newly identified genes and those of POU5F1 were aligned to their mammalian orthologs to determine the degree of evolutionary conservation
Higher values of OCT-4 expression were observed in embryos and endometrial tissue in females reproduced under heat conditions.
protein expression during rabbit embryonic development: investigation of temporal and spatial relationship of expression of Oct-4, Cdx-2 (caudal type homeobox transcription factor 2 (show CDX2 ELISA Kits)) and histone H4 (acetylated at lysine 5) in morula/blastocysts
The signal may have reflected the regulation of Oct-4 through enhancer switching and therefore may be related to cell lineage formation in rabbit embryos.
The POU5F1 gene is strictly regulated during early embryo development.
Chromatin accessibility at OCT4-bound sites requires the chromatin remodeller BRG1 (show SMARCA4 ELISA Kits), which is recruited to these sites by OCT4 to support additional transcription factor binding and expression of the pluripotency-associated transcriptome.
data infer that OCT4 expression may have a direct effect on partial cardiomyocyte reprogramming of MSCs and suggest a new mechanism(s) associated with MSC (show MSC ELISA Kits) multipotency and a requirement for crosstalk with the cardiac microenvironment
Regulation of Oct4 by SirT1 (show SIRT1 ELISA Kits) may link stem cell development to environmental conditions, and it may provide strategies to manipulate epiblast cell state.
we suggest that the activity of Oct4 DE and PE is regulated by the repressive histone marks and DNA methylation (show HELLS ELISA Kits) in a cell-type-specific manner.
PRDM14 (show PRDM14 ELISA Kits) recruited OCT3/4 to the enhancer regions of naive pluripotency genes via TET-base excision repair-mediated demethylation.
High POU5F1 expression is associated with disruption in differentiation and spermatogenesis.
Three regulating complexes centered by Sox2 (show SOX2 ELISA Kits)-Oct4, Nanog (show NANOG ELISA Kits), and Lrh1 (show NR5A2 ELISA Kits) maintain Oct4 expression in pluripotent stem cells in mice. [review]
OCT4 is an integral and necessary component of signal-regulated transcriptional processes required for tissue-specific responses.
Maintenance of pluripotency is regulated by a network of transcription factors coordinated by Oct4, Sox2 (show SOX2 ELISA Kits), and Nanog (show NANOG ELISA Kits); Trim24 (show TRIM24 ELISA Kits) significantly improved efficiency of cellular reprogramming, demonstrating its direct functionality in establishing pluripotency.
ATOX1 (show ATOX1 ELISA Kits) appeared ubiquitously expressed throughout the cells until compaction; in subsequent embryo stages, ATOX1 (show ATOX1 ELISA Kits) relocalized to cytoplasmic perinuclear domains in the inner cell mass. Silencing of Oct4 did not affect Atox1 (show ATOX1 ELISA Kits) expression, but silencing of Atox1 (show ATOX1 ELISA Kits) at the 2-cell stage strongly diminished Oct4 expression in 16-cell embryos.
Activin A (show INHBA ELISA Kits) and overexpression of SMAD2 (show SMAD2 ELISA Kits)/3 significantly promoted expressions of porcine NANOG (show NANOG ELISA Kits) and OCT4,maintaining induced pluripotent stem cell self-renewal through up-regulation of Nanog (show NANOG ELISA Kits)/OCT4 expression.
Our results indicate that continuous expression of OCT-4 in blastomeres is essential for trophectoderm formation of porcine embryos.
These findings suggest that the 12-bp indel polymorphism of the Oct4 gene might be a potential DNA marker for selecting preferred individuals in relation to reproductive traits in pig marker-assisted selection breeding.
Oct4-overexpression enhances porcine ovarian stem cell differentiation in to oocyte-like cells.
showed novel molecular regulation of CDX2 (show CDX2 ELISA Kits) on Oct4, and provided important clues for clarifying the mechanism of interaction between CDX2 (show CDX2 ELISA Kits) and Oct4 in embryo of mammals other than mouse
Overexpression of Sox2 (show SOX2 ELISA Kits) or Oct4 in bone mesenchymal stem cells in culture media containing a basic fibroblast growth factor (show FGF2 ELISA Kits) results in higher proliferation and differentiation compared to controls.
Oct4 positive stem/progenitor swine lung epithelial cells are targets for influenza virus replication.
study shows that localization of octamer-binding protein 4(OCT4) is associated with an embryonic stem cell (ESC)-like morphology from porcine inner cell mass
OCT4 expression, in contrast to earlier speculations, at least in hatched blastocysts, resembles the expression pattern in the mouse embryo.
cells isolated from umbilical cord express three transcription factors,Oct-4, Sox-2 & Nanog, found in pluripotent stem cell markers both at the mRNA and protein level.
we concluded that OCT4 expression in somatic cells is not a good prognosis marker for selecting cell lines.
analysis of pluripotency gene expression of OCT4, SOX2 and NANOG and mRNA levels of some of their downstream targets in bovine oocytes and early embryos
Oct4 exhibited significant hypermethylation in sperm compared with that in oocytes
In contrast to protein distribution, regulation of Oct4 transcription is conserved between mammalian species.
analysis of CpG islands of bovine Leptin (show LEP ELISA Kits) and POU5F1 genes in cloned bovine fetuses
The restoration of pluripotency can be directly observed in living cells or SCNT embryos from such Pou5f1-EGFP transgenic fetuses.
Oct4 cDNA and a 2.8-kb regulatory region upstream of its start codon were isolated and characterized
evaluated pattern of POU5F1 expression during early embryo development;study shows POU5F1 protein is present in cytoplasm and nucleus of immature oocytes, decreases during embryo development to day 5, then increases again within embryonic nuclei [POU5F1]
This gene encodes a transcription factor containing a POU homeodomain. This transcription factor plays a role in embryonic development, especially during early embryogenesis, and it is necessary for embryonic stem cell pluripotency. A translocation of this gene with the Ewing's sarcoma gene, t(6\;22)(p21\;q12), has been linked to tumor formation. Alternative splicing, as well as usage of alternative translation initiation codons, results in multiple isoforms, one of which initiates at a non-AUG (CUG) start codon. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12.
POU domain transcription factor OCT4
, POU domain, class 5, transcription factor 1
, POU-type homeodomain-containing DNA-binding protein
, octamer-binding protein 3
, octamer-binding protein 4
, octamer-binding transcription factor 3
, octamer-binding transcription factor-3
, POU class 5 homeobox 1
, POU domain, class 5, transcription factor 1-like
, POU domain class 5 transcription factor 1
, POU domain gene 2
, spiel ohne grenzen
, spiel ohne grenzen/pou2
, octamer binding transcription factor 4
, Octamer-binding transcription factor 3
, octamer-binding transcription factor 4