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CREB1 — CREM
Pathways - manually collected, often from reviews:
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
Text-mined interactions from Literome
Wang et al., Mol Cell Biochem 2000
:
Although
CREB transcription is activated by multiple classes of agonists in VSMC, and
ICER can
inhibit agonist induced transcription mediated by both CREB and AP-1 enhancers, these transcription factors are not obligate components of the pathways regulating AT1-R gene expression in rat VSMC
Don et al., Mol Cell Endocrinol 2002
:
Inducible cAMP early repressor (ICER) , a suppressor isoform of CREM, also activated by CREB, down
regulates CREB expression together with its own expression, resetting CREB to basal level that enables a new spermatogenic wave
Mouravlev et al., Brain Res 2007
:
Here we found that transient expression of a CREB dominant interfering mutant A-CREB or the inducible cAMP early repressor,
ICER ,
led to the dramatic decrease of exogenously co-expressed
CREB in 293 human embryonic kidney cells ... Hence, heterodimerization of unphosphorylated CREB with either A-CREB or
ICER triggers CREB protein degradation, whereas phosphorylation prevents CREB from such degradation both in vitro and in vivo
Steinbicker et al., Nitric Oxide 2011
:
Expression of a dominant negative
CREB in RPaSMC
prevented the NO-mediated induction of CRE dependent gene transcription and
ICER gene expression ... Our results suggest that induction of
ICER gene expression by NO
requires both
CREB phosphorylation and Ca ( 2+ ) signaling
Favre et al., Diabetes 2011
(Obesity) :
In this study, we investigated whether impaired expression of the
inducible cAMP early repressor (ICER) , a transcriptional antagonist of CREB, is
responsible for the increased
CREB activity in adipocytes of obese mice and humans
Lamas et al., Mol Endocrinol 1997
:
Thus, while phosphorylation of cAMP response element binding protein ( CREB ) by the cAMP dependent protein kinase A is the prerequisite for induction, it has been proposed that the following attenuation involves both
CREB dephosphorylation and
repression by the inducible repressor
ICER
Monaco et al., Oncogene 1997
:
Both
CREB phosphorylation and
ICER inducibility require an intact Ras dependent signalling pathway
Walker et al., Mol Cell Endocrinol 1998
:
We suggest that the expression of
ICER in Sertoli cells may
contribute to the periodic repression of
CREB gene expression during the repeated 12-day cycles of spermatogenesis, and may be required to reset the levels of activator CREB prior to the initiation of each new cycle of spermatogenesis