Enhancer ID: | E_01_342 | |
Enhancer symbol: | -- | |
Species: | Human | |
Position : | chr19:15308673-15308842 |
|
Biosample name: | T-acute lymphoblastic leukemia (T-ALL) | |
Experiment class : | Low throughput |
Enhancer type: | Super-Enhancer | |
Disease: | Central Nervous System Leukemia | |
DO: | DOID:12969 | |
Mesh: | -- | |
Distance from TSS: | >2KB | |
Pubmed ID: | 30518632 |
Enhancer experiment: | ChIP-qPCR,qRT-PCR,ChIP,Transgenic mice | |
Enhancer experiment description: | We found robust cytotoxicity against T-ALL cells, but not normal bone marrow progenitors, for two N-alkylated TCP derivatives, S2116 and S2157. The two compounds induced apoptosis in TCP-resistant T-ALL cells in vitro and in vivo by repressing transcription of the NOTCH3 and TAL1 genes through increased H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. |
Target gene : | NOTCH3(CADASIL,CADASIL1,CASIL,IMF2,LMNS) | |
Strong evidence: | -- | |
Less strong evidence: | qRT-PCR,ChIP | |
Target gene experiment description: | we found that both S2116 and S2157 readily increased the methylation level of H3K9 and reciprocally reduced the acetylation level of H3K27 at Super-Enhancer regions of the NOTCH3 and TAL1 genes (GRCh38/hg38: 15,198,031-15,197,862 and GRCh38/hg38: 47,239,435-47,239,119,respectively) using ChIP assays.In addition,global ChIP-seq analyses revealed that the acetylation level of H3K27 was readily decreased by LSD1 inhibition through the entire range of NOTCH3 and TAL1 Enhancers. |
TF name : | ZEB2(HSPC082,SIP-1,SIP1,SMADIP1,ZFHX1B) | |
TF experiment: | RT-PCR | |
TF experiment description: | We used the Expression Assays(Hs01097987 for TAL1, Hs01128537 for NOTCH3, Hs00207691 for ZEB2, and Hs01922876 forGAPDH) and TaqMan Universal PCR Master Mix (Applied Biosystems, Waltham, MA) for real-time quantitative RT-PCR (RQ-PCR). |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
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SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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