+ |
NODAL | up-regulates quantity by expression
transcriptional regulation
|
TDGF1 |
0.648 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251942 |
|
|
Homo sapiens |
GBM-8401 Cell |
pmid |
sentence |
20383200 |
Nodal induced LIF and Cripto-1 expressions through Smad2 signaling pathway. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TDGF1 | down-regulates activity
binding
|
TGFB1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-150006 |
|
|
Homo sapiens |
|
pmid |
sentence |
17030617 |
Ere, we provide evidence supporting a novel mechanism in which Cripto inhibits the tumor suppressor function of TGF-beta. Cripto bound TGF-beta and reduced the association of TGF-beta with its type I receptor, TbetaRI. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TDGF1 | up-regulates activity
binding
|
NODAL |
0.648 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251937 |
|
|
Homo sapiens |
|
pmid |
sentence |
19874624 |
Nodal effects are dependent upon interactions with Cripto, a small cysteine-rich extracellular protein that is attached to the plasma membrane through a glycosyl phosphatidyl inositol linkage. Cripto interacts with Nodal and ALK4, independently, and promotes the formation of a stable high affinity complex with activin type II receptors. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SOX2/POU5F1 | up-regulates quantity by expression
transcriptional regulation
|
TDGF1 |
0.624 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269236 |
|
|
|
|
pmid |
sentence |
31583686 |
Both SOX2 and SOX17 are able to partner with OCT4 and, as a consequence, recognize and bind specific binding motifs.6, 7 In human and mouse ESCs, SOX2/OCT4 bind to canonical motifs (CTTTGTCATGCAAAT-like), which are composite SOX (CATTGTC-like) and OCT (ATGCAAAT-like) motifs|This way SOX17 and SOX2 regulate a common set of pluripotency and GC-related genes (PRDM14, DPPA4, TDGF1, NANOG, LIN28A, TRIM71, OTX2, PIM2) (Fig. 6). Additionally, in TCam-2 cells SOX17 binds to compressed motifs or SOX motifs (not bound by SOX2 in ECs), thereby regulating the PGC specifiers PRDM1 and TFAP2C, the GC-related genes NANOS3 and BMP7 and the cancer-related genes MYC and IGF1 (Fig. 6). In 2102EP cells, SOX2 further binds canonical elements or SOX motifs (not bound by SOX17 in TCam-2), regulating additional pluripotency genes (GDF3, LEFTY2, SALL4, SOX2 and POU5F1) (Fig. 6). |
|
Publications: |
1 |
+ |
POU5F1 | up-regulates quantity by expression
transcriptional regulation
|
TDGF1 |
0.676 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254943 |
|
|
Homo sapiens |
Embryonic Stem Cell |
pmid |
sentence |
17068183 |
To enhance our understanding of the molecular basis of this differentiation event in humans, we used a functional genomics approach involving RNA interference-mediated suppression of OCT4 function in a human ESC line and analysis of the resulting transcriptional profiles to identify OCT4-dependent genes in human cells. We detected altered expression of >1,000 genes, including targets regulated directly by OCT4 either positively (NANOG, SOX2, REX1, LEFTB, LEFTA/EBAF DPPA4, THY1, and TDGF1) or negatively (CDX2, EOMES, BMP4, TBX18, Brachyury [T], DKK1, HLX1, GATA6, ID2, and DLX5), as well as targets for the OCT4-associated stem cell regulators SOX2 and NANOG. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TDGF1 | down-regulates
|
MSTN |
0.318 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-192436 |
|
|
Homo sapiens |
|
pmid |
sentence |
23129614 |
We provide evidence that cripto modulates myogenic cell determination and promotes proliferation by antagonizing the tgf-beta ligand myostatin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TDGF1 | up-regulates activity
binding
|
ACVR1B |
0.717 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251938 |
|
|
Homo sapiens |
|
pmid |
sentence |
19874624 |
Nodal effects are dependent upon interactions with Cripto, a small cysteine-rich extracellular protein that is attached to the plasma membrane through a glycosyl phosphatidyl inositol linkage. Cripto interacts with Nodal and ALK4, independently, and promotes the formation of a stable high affinity complex with activin type II receptors. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SOX17/POU5F1 | up-regulates quantity by expression
transcriptional regulation
|
TDGF1 |
0.519 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269244 |
|
|
|
|
pmid |
sentence |
31583686 |
Both SOX2 and SOX17 are able to partner with OCT4 and, as a consequence, recognize and bind specific binding motifs.6, 7 In human and mouse ESCs, SOX2/OCT4 bind to canonical motifs (CTTTGTCATGCAAAT-like), which are composite SOX (CATTGTC-like) and OCT (ATGCAAAT-like) motifs|This way SOX17 and SOX2 regulate a common set of pluripotency and GC-related genes (PRDM14, DPPA4, TDGF1, NANOG, LIN28A, TRIM71, OTX2, PIM2) (Fig. 6). Additionally, in TCam-2 cells SOX17 binds to compressed motifs or SOX motifs (not bound by SOX2 in ECs), thereby regulating the PGC specifiers PRDM1 and TFAP2C, the GC-related genes NANOS3 and BMP7 and the cancer-related genes MYC and IGF1 (Fig. 6). In 2102EP cells, SOX2 further binds canonical elements or SOX motifs (not bound by SOX17 in TCam-2), regulating additional pluripotency genes (GDF3, LEFTY2, SALL4, SOX2 and POU5F1) (Fig. 6). |
|
Publications: |
1 |
+ |
TDGF1 | up-regulates
|
Skeletal_muscle_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-192439 |
|
|
Homo sapiens |
Satellite Cell |
pmid |
sentence |
23129614 |
Cripto, a regulator of early embryogenesis, is a novel regulator of muscle regeneration and satellite cell progression toward the myogenic lineage. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Muscle, Skeletal Muscle |
+ |
TDGF1 | down-regulates
binding
|
ACVR2A |
0.627 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-100052 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
12682303 |
Here we show that cripto can form a complex with activin and actrii/iib cripto inhibited crosslinking of activin to alk4 and the association of alk4 with actrii/iib. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |