Enhancer ID: | E_02_134 | |
Enhancer symbol: | -- | |
Species: | Mouse | |
Position : | chr8:106610150-106612150 |
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Biosample name: | Non-tumorigenic Mouse Mammary Gland Cells | |
Experiment class : | Low throughput |
Enhancer type: | Enhancer | |
Disease: | -- | |
DO: | -- | |
Mesh: | -- | |
Distance from TSS: | >2KB | |
Pubmed ID: | 25652130 |
Enhancer experiment: | Luciferase Reporter Assay,3C | |
Enhancer experiment description: | We reported previously that intron 2 of Cdh1 is essential for proper E-cad expression.In order to analyze this large DNA sequence(>43 kb) for putative enhancers we focused on evolutionary conserved sequences. |
Target gene : | Cdh1(Arc-1,BCDS1,CD324,CDHE,ECAD,LCAM,UVO) | |
Strong evidence: | 3C | |
Less strong evidence: | ChIP,qPCR | |
Target gene experiment description: | We show that Cdh1 activity during MET is governed by two Enhancers at +7.8 kb and at +11.5 kb within intron 2 that are activated by binding of Grhl3 and Hnf4α,respectively. |
TF name : | Grhl3(SOM,TFCP2L4,VWS2)Hnf4a(HNF-4,Hnf4lpha,MODY1,Nr2a1,TCF-14,Tcf14,Hnf4a) | |
TF experiment: | Luciferase Reporter Assay,ChIP | |
TF experiment description: | Using luciferase reporter assays,we first tested whether Hnf4α could activate Cl.5 in NMuMG cells.We found that indeed Hnf4α was able to exert a robust enhancing effect on the E-cad Cl.5 reporter construct.Two different mutations in the putative Hnf4α binding site decreased the basal activity of this construct and inhibited its Hnf4α dependent activation. |
Enhancer function : | Enhancer cooperativity as a novel mechanism underlying the transcriptional regulation of E-cadherin during mesenchymal to epithelial transition. |
Enhancer function experiment: | ChIP |
Enhancer function experiment description: |
Enhancer cooperativity as a novel mechanism underlying the transcriptional regulation of E-cadherin during mesenchymal to epithelial transition. |
SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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