Enhancer ID: | E_01_418 | |
Enhancer symbol: | -- | |
Species: | Human | |
Position : | chr5:172196326-172199378 |
|
Biosample name: | MCF-7,MDA-MB-231 | |
Experiment class : | Low+High throughput |
Enhancer type: | Enhancer | |
Disease: | Breast Cancer | |
DO: | DOID:1612 | |
Mesh: | D001943 | |
Distance from TSS: | >2KB | |
Pubmed ID: | 26859151 |
Enhancer experiment: | ChIP-seq | |
Enhancer experiment description: | Similar co-localisation studies were conducted in MDA-MB-231 cells to further understand the potential contribution of DUSP family members in the mesenchymal state. Similar to above, DUSP1 showed high levels of co-localization with the active promoter marks H3K9me1 (PCC = 0.65) and H3K4me3 (PCC = 0.72) (Fig 2E), while DUSP4 showed definite co-localisa_x0002_tion with the enhancer marks H3K27ac (PCC = 0.56) and strong co-localisation with H3K4me1 (PCC = 0.78) (Fig 2F) but not H3K4me3 or H3K9me3 (Fig C in S2 Fig). |
Target gene : | DUSP1(CL100,HVH1,MKP-1,MKP1,PTPN10) | |
Strong evidence: | -- | |
Less strong evidence: | ChIP,RT-qPCR | |
Target gene experiment description: | Interestingly, we found that siRNA-mediated knockdown of DUSP1 and DUSP4 does not affect the expression of these genes (data not shown). Taken together,these data indicate a novel chromatin-anchored role for DUSP1 and DUSP4 in mesenchymal breast cancer cells. |
TF name : | -- | |
TF experiment: | -- | |
TF experiment description: | -- |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
-- |
SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
Home | Browse | Search | Download | Genome-Browser | Submit | Contact | Help
Copyright © HMU | 黑ICP备16009434号-1 | Li C Lab