+ |
CSNK1A1 | down-regulates quantity by destabilization
phosphorylation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276936 |
Ser38 |
TEMTASSsSDYGQTS |
in vitro |
|
pmid |
sentence |
26344095 |
Using in vitro kinase assays, we further demonstrated that deletion of degron 1 largely abolished CKI-mediated phosphorylation of ERG (Figure S5B), indicating that serine residues within degron 1 are the major CKI phosphorylation sites. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276935 |
Ser39 |
EMTASSSsDYGQTSK |
in vitro |
|
pmid |
sentence |
26344095 |
Using in vitro kinase assays, we further demonstrated that deletion of degron 1 largely abolished CKI-mediated phosphorylation of ERG (Figure S5B), indicating that serine residues within degron 1 are the major CKI phosphorylation sites. |
|
Publications: |
2 |
Organism: |
In Vitro |
+ |
GSK3B | down-regulates quantity by destabilization
phosphorylation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277528 |
Thr180 |
KDDFQRLtPSYNADI |
Homo sapiens |
Prostate Cancer Cell Line |
pmid |
sentence |
32871104 |
Here, we demonstrate that DNA damage induces proteasomal degradation of wild-type ERG and TMPRSS2-ERG oncoprotein through ERG threonine-187 and tyrosine-190 phosphorylation mediated by GSK3β and WEE1, respectively. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
WEE1 | down-regulates quantity by destabilization
phosphorylation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277529 |
Tyr183 |
FQRLTPSyNADILLS |
Homo sapiens |
Prostate Cancer Cell Line |
pmid |
sentence |
32871104 |
Here, we demonstrate that DNA damage induces proteasomal degradation of wild-type ERG and TMPRSS2-ERG oncoprotein through ERG threonine-187 and tyrosine-190 phosphorylation mediated by GSK3β and WEE1, respectively. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TAL1 | up-regulates quantity by expression
transcriptional regulation
|
ERG |
0.28 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253924 |
|
|
Homo sapiens |
T-cell Acute Lymphoblastic Leukemia Cell |
pmid |
sentence |
21536859 |
We further demonstrate that ERG expression in primary human T-ALL cells is mediated by the binding of other T-cell oncogenes SCL/TAL1, LMO2, and LYL1 in concert with ERG, FLI1, and GATA3 to the ERG +85 enhancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
WNT1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261597 |
|
|
Mus musculus |
LNCaP Cell |
pmid |
sentence |
23913826 |
Interestingly, our data showed that ERG drastically induced Wnt ligand gene expression. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
LYL1 | up-regulates quantity by expression
transcriptional regulation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253923 |
|
|
Homo sapiens |
|
pmid |
sentence |
21536859 |
We further demonstrate that ERG expression in primary human T-ALL cells is mediated by the binding of other T-cell oncogenes SCL/TAL1, LMO2, and LYL1 in concert with ERG, FLI1, and GATA3 to the ERG +85 enhancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
TDRD1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254067 |
|
|
Homo sapiens |
VCaP Cell |
pmid |
sentence |
23319146 |
In the prostate cancer cell line VCaP, downregulation of ERG by shRNA lead to a lower expression level of TDRD1 and resulted in a decreased activity of the TDRD1 promoter. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254068 |
|
|
Homo sapiens |
Prostate Cancer Cell Line |
pmid |
sentence |
23555854 |
we report that ERG and TDRD1 are co-expressed in human prostate cancers and we provide a mechanistic explanation for the observed co-expression. We demonstrate that ERG activates TDRD1 transcription by inducing loss of DNA methylation at the TDRD1 promoter-associated CpG island. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
ADAMTS1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253910 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
19396168 |
ADAMTS1 and CXCR4, two candidate genes strongly associated with cell migration, were upregulated in the presence of ERG overexpression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | down-regulates quantity by repression
transcriptional regulation
|
EPB41L3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253918 |
|
|
Homo sapiens |
|
pmid |
sentence |
20860828 |
EPB41L3 downregulation and EPB41L4B upregulation were essentially restricted to the 22 cases with ERG overexpression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
EPB41L4B |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253919 |
|
|
Homo sapiens |
|
pmid |
sentence |
20860828 |
EPB41L3 downregulation and EPB41L4B upregulation were essentially restricted to the 22 cases with ERG overexpression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
WNT11 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254071 |
|
|
Homo sapiens |
|
pmid |
sentence |
21242973 |
ERG transcriptional networks in leukemia converge on WNT signaling targets. Specifically, WNT11 emerged as a direct target of ERG. Small interfering RNA (siRNA)-mediated knockdown of ERG confirmed downregulation of WNT11 transcripts. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | down-regulates quantity by repression
transcriptional regulation
|
NKX3-1 |
0.341 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251556 |
|
|
Homo sapiens |
|
pmid |
sentence |
25277175 |
Increased expression of ERG or other ETS factors under control of androgen responsive promoter (TMPRSS2) is an inevitable consequence of the fusion events, and it activates transcriptional program that contributes to oncogenesis by upregulating expression of, among others, MYC, EZH2 and SOX9 and repressing NKX3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Prostate Cancer |
+ |
FLI1 | up-regulates quantity by expression
transcriptional regulation
|
ERG |
0.317 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253921 |
|
|
Homo sapiens |
T-cell Acute Lymphoblastic Leukemia Cell |
pmid |
sentence |
21536859 |
We further demonstrate that ERG expression in primary human T-ALL cells is mediated by the binding of other T-cell oncogenes SCL/TAL1, LMO2, and LYL1 in concert with ERG, FLI1, and GATA3 to the ERG +85 enhancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
ENG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253916 |
|
|
Homo sapiens |
|
pmid |
sentence |
22235125 |
It has been shown that ERG is a positive regulator of several EC-restricted genes including VE-cadherin, endoglin, and von Willebrand factor, and a negative regulator of other genes such as interleukin (IL)-8 and intercellular adhesion molecule (ICAM)-1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | down-regulates quantity by repression
transcriptional regulation
|
CXCL8 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253912 |
|
|
Homo sapiens |
HUVEC Cell |
pmid |
sentence |
19359602 |
ERG can inhibit the activity of the IL-8 promoter in a dose dependent manner. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
CXCR4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253911 |
|
|
Homo sapiens |
|
pmid |
sentence |
19396168 |
ADAMTS1 and CXCR4, two candidate genes strongly associated with cell migration, were upregulated in the presence of ERG overexpression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
LMO2 | up-regulates quantity by expression
transcriptional regulation
|
ERG |
0.39 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253922 |
|
|
Homo sapiens |
T-cell Acute Lymphoblastic Leukemia Cell |
pmid |
sentence |
21536859 |
We further demonstrate that ERG expression in primary human T-ALL cells is mediated by the binding of other T-cell oncogenes SCL/TAL1, LMO2, and LYL1 in concert with ERG, FLI1, and GATA3 to the ERG +85 enhancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
VIM |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254069 |
|
|
Homo sapiens |
MCF-7 Cell, MDA-MB-231 Cell |
pmid |
sentence |
8895512 |
Our results suggest that PEA3 specifically transactivates vimentin promoter through PEA3 site. Among members of the ETS transcription factor family only Erg showed ability to transactivate vimentin promoter besides PEA3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
PIM |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259408 |
|
|
Homo sapiens |
Prostate Epithelium Cell Line |
pmid |
sentence |
22140532 |
ERG deregulation induces PIM1 over-expression and aneuploidy in prostate epithelial cells. The up-regulation of PIM1 induced by tERG over-expression significantly modified Cyclin B1 levels and increased the percentage of aneuploid cells in the RWPE-1 cell line after taxane-based treatment. Here we provide the first evidence for an ERG-mediated PIM1 up-regulation in prostate cells in vitro and in vivo, suggesting a direct effect of ERG transcriptional activity in the alteration of genetic stability. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
WNT3A |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261598 |
|
|
Mus musculus |
LNCaP Cell |
pmid |
sentence |
23913826 |
Interestingly, our data showed that ERG drastically induced Wnt ligand gene expression. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
VWF |
0.25 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253914 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
9444957 |
Cotransfection of Ets-1 and Erg expression plasmids is sufficient to induce the -60/+19 vWF promoter activity in HeLa cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM6A | down-regulates quantity by repression
transcriptional regulation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260033 |
|
|
Homo sapiens |
|
pmid |
sentence |
29736013 |
Our findings reveal a dual role for UTX in suppressing acute myeloid leukaemia via repression of oncogenic ETS and upregulation of tumor suppressive GATA programs. several ETS transcription factors, including Elf4, Etv6, Erg, Fli1, Ets2, Spi1 and Elk3 were upregulated immediately after Utx loss in the preleukaemic phase |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RAD21 | down-regulates activity
relocalization
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261515 |
|
|
Homo sapiens |
Acute Myeloid Leukemia Cell |
pmid |
sentence |
26607380 |
Large-scale AML genome re-sequencing efforts have identified novel recurrently mutated genes, including the members of the cohesin complex (RAD21, SMC3, SMC1A, and STAG2), implicated in the pathogenesis of this disease.Using ATAC-seq, we determined that mutant cohesin lead to a state of elevated chromatin accessibility and higher predicted binding at transcription factor binding sites for ERG, GATA2, and RUNX1. Moreover, using ChIP-Seq, we formally demonstrated increased binding of GATA2 and RUNX1 to these sites. Finally, we demonstrated that knockdown of these three TFs in human HSPC can revert the differentiation block induced by mutant cohesin. These results support a model in which mutant cohesin impairs hematopoietic differentiation and enforces stem cell programs through the modulation of ERG, GATA2, and RUNX1 chromatin accessibility, expression, and activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
PIM1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254065 |
|
|
Homo sapiens |
|
pmid |
sentence |
22140532 |
ERG deregulation induces PIM1 over-expression and aneuploidy in prostate epithelial cells. The up-regulation of PIM1 induced by tERG over-expression significantly modified Cyclin B1 levels and increased the percentage of aneuploid cells in the RWPE-1 cell line after taxane-based treatment. Here we provide the first evidence for an ERG-mediated PIM1 up-regulation in prostate cells in vitro and in vivo, suggesting a direct effect of ERG transcriptional activity in the alteration of genetic stability. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253925 |
|
|
Homo sapiens |
T-cell Acute Lymphoblastic Leukemia Cell |
pmid |
sentence |
21536859 |
We further demonstrate that ERG expression in primary human T-ALL cells is mediated by the binding of other T-cell oncogenes SCL/TAL1, LMO2, and LYL1 in concert with ERG, FLI1, and GATA3 to the ERG +85 enhancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Prostate Cancer |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
SPP1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254066 |
|
|
Homo sapiens |
|
pmid |
sentence |
21669963 |
Using in vitro and in vivo molecular assays, we showed that ERG increases OPN expression and binds to an EBS (nt -115 to -118) in the OPN promoter. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GATA3 | up-regulates quantity by expression
transcriptional regulation
|
ERG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253920 |
|
|
Homo sapiens |
|
pmid |
sentence |
21536859 |
We further demonstrate that ERG expression in primary human T-ALL cells is mediated by the binding of other T-cell oncogenes SCL/TAL1, LMO2, and LYL1 in concert with ERG, FLI1, and GATA3 to the ERG +85 enhancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
EZH2 |
0.351 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251555 |
|
|
Homo sapiens |
|
pmid |
sentence |
25277175 |
Increased expression of ERG or other ETS factors under control of androgen responsive promoter (TMPRSS2) is an inevitable consequence of the fusion events, and it activates transcriptional program that contributes to oncogenesis by upregulating expression of, among others, MYC, EZH2 and SOX9 and repressing NKX3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Prostate Cancer |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
MYC |
0.287 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251554 |
|
|
Homo sapiens |
|
pmid |
sentence |
25277175 |
Increased expression of ERG or other ETS factors under control of androgen responsive promoter (TMPRSS2) is an inevitable consequence of the fusion events, and it activates transcriptional program that contributes to oncogenesis by upregulating expression of, among others, MYC, EZH2 and SOX9 and repressing NKX3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Prostate Cancer |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
CDH5 |
0.281 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261595 |
|
|
Homo sapiens |
|
pmid |
sentence |
18195090 |
Erg overexpression resulted in an approximate 1.8-fold transactivation of VE-cadherin promoter activity. Thus, our data indicate that Erg drives constitutive VE-cadherin expression in human ECs |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | down-regulates quantity by repression
transcriptional regulation
|
ICAM1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253917 |
|
|
Homo sapiens |
|
pmid |
sentence |
22235125 |
It has been shown that ERG is a positive regulator of several EC-restricted genes including VE-cadherin, endoglin, and von Willebrand factor, and a negative regulator of other genes such as interleukin (IL)-8 and intercellular adhesion molecule (ICAM)-1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
CLDN5 |
0.225 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261596 |
|
|
Homo sapiens |
|
pmid |
sentence |
22235125 |
ETS-related gene (ERG) controls endothelial cell permeability via transcriptional regulation of the claudin 5 (CLDN5) gene. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
ICAM2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253913 |
|
|
Homo sapiens |
|
pmid |
sentence |
10574717 |
The Ets family member Erg was found to be constitutively expressed in HUVEC, and TNF-(alpha) down-regulated Erg protein levels. Furthermore, an Erg cDNA transactivated the ICAM-2 promoter when transiently transfected into both HeLa cells and HUVEC. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |