Enhancer ID: | E_02_087 | |
Enhancer symbol: | -- | |
Species: | Mouse | |
Position : | chr4:124638991-124641160 |
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Biosample name: | Mouse Embryonic Stem Cell | |
Experiment class : | Low+High throughput |
Enhancer type: | Enhancer | |
Disease: | -- | |
DO: | -- | |
Mesh: | -- | |
Distance from TSS: | >2KB | |
Pubmed ID: | 24905168 |
Enhancer experiment: | ChIP-seq,RNA-seq | |
Enhancer experiment description: | To address whether changes in enhancer utilization patterns occur in the majority of cells within the differentiating population, we isolated dual transgenic enhancer reporter lines, in which ESC-specific or EpiLC-specific enhancers of interest were cloned upstream of a minimal promoter and one of two distinct fluorescent reporters and integrated into the ESC genome using a PiggyBac transposon system. |
Target gene : | Pou3f1(Oct-6,Oct6,Otf-6,Otf6,Scip,Test1,Tst-1,Tst1) | |
Strong evidence: | -- | |
Less strong evidence: | qPCR,IP-Western | |
Target gene experiment description: | Upon differentiation, Otx2−/− cells underwent morphological changes indistinguishable from those seen in wt EpiLCs, but showed defects in expression of certain epiblast-associated genes, such as Fgf5 and Oct6. RNA-seq analysis of Otx2−/− EpiLCs identified 260 and 141 genes significantly downregulated or upregulated, respectively, as compared to the genetically-matched wt EpiLCs |
TF name : | Otx2(E130306E05Rik)Oct4 | |
TF experiment: | ChIP-seq | |
TF experiment description: | Our results illuminate regulatory mechanisms underlying pluripotency and suggest that capacity of transcription factors such as Otx2 and Oct4 to pioneer new Enhancer sites is highly context dependent. |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
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SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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