Interaction |
Interaction target |
Level of interaction |
Type of interaction |
Description |
PMID |
Source |
mPus1p |
RNA-Protein |
regulation |
Mpus1p-coactivator function required sra, mpus1p-associated mrargamma binding, and pus activities. |
15327771
|
|
MyoD |
RNA-Protein |
binding |
We have found that the RNA helicases p68/p72 are MyoD-associated proteins and that the noncoding RNA SRA also immunoprecipitates with MyoD. |
17011493
|
LncRNADisease |
p68 |
RNA-Protein |
binding |
One of the RNAs associated with p68/p72 is the noncoding Steroid Receptors RNA Activator (SRA). |
17495528
|
LncRNADisease |
p72 |
RNA-Protein |
binding |
One of the RNAs associated with p68/p72 is the noncoding Steroid Receptors RNA Activator (SRA). |
17495528
|
LncRNADisease |
CCL20 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
DIO2 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
SLC2A12 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
SLC2A3 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
TBL1X |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
TGFB2 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
TMEM65 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
TMPRSS2 |
RNA-Protein |
binding |
Eight bona fide SRA downstream target genes were identified (SLC2A3, SLC2A12, CCL20, TGFB2, DIO2, TMEM65, TBL1X, and TMPRSS2). |
20219889
|
LncRNADisease |
SHARP |
RNA-DNA |
regulation |
SRA is sequestered by the transcriptionally silent TRa2 to a repressive protein complex containing RNA-binding proteins SHARP and SLIRP. |
20573714
|
LncRNADisease |
SLIRP |
RNA-DNA |
regulation |
SRA is sequestered by the transcriptionally silent TRa2 to a repressive protein complex containing RNA-binding proteins SHARP and SLIRP. |
20573714
|
LncRNADisease |
TRa2 |
RNA-Protein |
binding |
SRA is sequestered by the transcriptionally silent TRa2 to a repressive protein complex containing RNA-binding proteins SHARP and SLIRP. |
20573714
|
LncRNADisease |
SRC1 |
RNA-Protein |
binding |
SRC1 complex is recruited by SRA. |
20573714
|
LncRNADisease |
MyoD |
RNA-RNA |
co-expression |
SRA ncRNA is known to increase the activity of a range of nuclear receptors as well as the master regulator of muscle differentiation MyoD. |
20855289
|
LncRNADisease |
CTCF |
RNA-Protein |
binding |
Here we showed that the DEAD-box RNA helicase p68 (DDX5) and its associated noncoding RNA, steroid receptor RNA activator (SRA), form a complex with CTCF that is essential for insulator function. |
20966046
|
LncRNADisease |
p68 |
RNA-Protein |
binding |
Here we showed that the DEAD-box RNA helicase p68 (DDX5) and its associated noncoding RNA, steroid receptor RNA activator (SRA), form a complex with CTCF that is essential for insulator function. |
20966046
|
LncRNADisease |
IGF2 |
RNA-RNA |
co-expression |
In vivo depletion of SRA or p68 reduced CTCF-mediated insulator activity at the IGF2/H19 ICR, increased levels of IGF2 expression, and increased interactions between the endodermal enhancer and IGF2 promoter. |
20966046
|
LncRNADisease |
cohesin complex |
RNA-Protein |
binding |
p68/SRA also interacts with members of the cohesin complex. |
20966046
|
LncRNADisease |
PPARG |
RNA-Protein |
binding |
We show that the non-coding RNA, Steroid receptor RNA Activator (SRA), associates with PPARgamma and coactivates PPARgamma-dependent reporter gene expression. |
21152033
|
LncRNADisease |
CTCF |
RNA-Protein |
binding |
DEAD-box RNA helicase p68 (DDX5) and its associated lncRNA, SRA (steroid receptor RNA activator), form a complex with CTCF. CTCF binds to specific genomic binding sequences and plays an important role in transcriptional insulation and long-range physical interaction with other CTCF sites. |
21496640
|
LncRNADisease |
DDX5 |
RNA-Protein |
binding |
DEAD-box RNA helicase p68 (DDX5) and its associated lncRNA, SRA (steroid receptor RNA activator), form a complex with CTCF. CTCF binds to specific genomic binding sequences and plays an important role in transcriptional insulation and long-range physical interaction with other CTCF sites. |
21496640
|
LncRNADisease |
Cisplatin and paclitaxel |
N/A |
regulation |
Cisplatin and paclitaxel have target function on significant lncRNAs in LSCC, which presents novel molecular targets to cure LSCC patients and also leads an orientation for developing new drugs. |
25257554
|
|
NANOG |
RNA-TF |
regulation |
NANOG was identified as a transcription factor directly interacting with SRA and co-localizing with it genome-wide in NTERA2. |
26496121
|
|
polycomb repressive complex 2 (PRC2) |
RNA-Protein |
binding |
The lncRNA steroid receptor RNA activator (SRA) participates in regulation through complex formation with trithorax group (TrxG) and polycomb repressive complex 2 (PRC2) complexes. Binding of the SRA-associated RNA helicase p68 preferentially stabilizes complex formation between SRA and a TrxG complex but not PRC2. In human pluripotent stem cells NTERA2, SRA binding sites that are also occupied by p68 are significantly enriched for H3K4 trimethylation. |
26496121
|
|
trithorax group (TrxG) |
RNA-Protein |
binding |
The lncRNA steroid receptor RNA activator (SRA) participates in regulation through complex formation with trithorax group (TrxG) and polycomb repressive complex 2 (PRC2) complexes. Binding of the SRA-associated RNA helicase p68 preferentially stabilizes complex formation between SRA and a TrxG complex but not PRC2. In human pluripotent stem cells NTERA2, SRA binding sites that are also occupied by p68 are significantly enriched for H3K4 trimethylation. |
26496121
|
|
|