+ |
CBFB | up-regulates quantity by stabilization
binding
|
RUNX1 |
0.841 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255712 |
|
|
Mus musculus |
|
pmid |
sentence |
11179217 |
We observed previously that the RUNX proteins are susceptible to proteolytic degradation (Ogawa et al., 1993b). In this study, we show that the ubiquitin‚proteasome system is largely responsible for this degradation. We also show that when PEBP2Œ≤ dimerizes with RUNX it inhibits the ubiquitylation of RUNX, which is necessary for the protein to be targeted for proteolysis by the proteasome. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255742 |
|
|
Mus musculus |
32D Clone3 Cell |
pmid |
sentence |
11179217 |
The RUNX genes encode the α subunit of the transcription factor PEBP2/CBF. The β subunit consists of the non-RUNX protein PEBP2β. We found that RUNX1/AML1, which is essential for hematopoiesis, is continuously subjected to proteolytic degradation mediated by the ubiquitin–proteasome pathway. When PEBP2β is present, however, the ubiquitylation of RUNX1 is abrogated and this causes a dramatic inhibition of RUNX1 proteolysis. |
|
Publications: |
2 |
Organism: |
Mus Musculus |
Pathways: | HaematopoiesisTranscriptionalControl |
+ |
MLL-ENL | down-regulates quantity by repression
transcriptional regulation
|
CBFB |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255854 |
|
|
Homo sapiens |
|
pmid |
sentence |
24449215 |
However, the functional consequence of MLL fusions on RUNX1/CBFβ activity has not been fully understood. In this report, we show that MLL fusion proteins and the N-terminal MLL portion of MLL fusions downregulate RUNX1 and CBFβ protein expression via the MLL CXXC domain and flanking regions. We found that MLL-BP and the 3 MLL fusion proteins all decreased RUNX1 levels, and MLL-eleven nineteen leukemia (ENL) caused a greater decrease in RUNX1 compared with MLL-AF9 and MLL-AF4 fusion proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MLL-AF9 | down-regulates quantity by repression
transcriptional regulation
|
CBFB |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255852 |
|
|
Homo sapiens |
|
pmid |
sentence |
24449215 |
However, the functional consequence of MLL fusions on RUNX1/CBFβ activity has not been fully understood. In this report, we show that MLL fusion proteins and the N-terminal MLL portion of MLL fusions downregulate RUNX1 and CBFβ protein expression via the MLL CXXC domain and flanking regions. We found that MLL-BP and the 3 MLL fusion proteins all decreased RUNX1 levels, and MLL-eleven nineteen leukemia (ENL) caused a greater decrease in RUNX1 compared with MLL-AF9 and MLL-AF4 fusion proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CBFB | form complex
binding
|
Core Binding Factor complex |
0.841 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255711 |
|
|
Homo sapiens |
|
pmid |
sentence |
12495904 |
The core binding factor (CBF) transcription complex, consisting of the interacting proteins RUNX1 and CBFβ, is essential for normal hematopoiesis |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MLL-AF4 | down-regulates quantity by repression
transcriptional regulation
|
CBFB |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255856 |
|
|
Homo sapiens |
|
pmid |
sentence |
24449215 |
However, the functional consequence of MLL fusions on RUNX1/CBFβ activity has not been fully understood. In this report, we show that MLL fusion proteins and the N-terminal MLL portion of MLL fusions downregulate RUNX1 and CBFβ protein expression via the MLL CXXC domain and flanking regions. We found that MLL-BP and the 3 MLL fusion proteins all decreased RUNX1 levels, and MLL-eleven nineteen leukemia (ENL) caused a greater decrease in RUNX1 compared with MLL-AF9 and MLL-AF4 fusion proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GATA1 | down-regulates quantity by repression
transcriptional regulation
|
CBFB |
0.491 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254190 |
|
|
Mus musculus |
MEL Cell |
pmid |
sentence |
19825991 |
Gene expression arrays identified components of the PU.1-dependent transcriptome negatively regulated by GATA-1 in MEL cells, including CCAAT/enhancer binding protein alpha (Cebpa) and core-binding factor, beta subunit (Cbfb), which encode two key hematopoietic transcription factors. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | HaematopoiesisTranscriptionalControl |