EID2
Description
The EID2 (EP300 interacting inhibitor of differentiation 2) is a protein-coding gene located on chromosome 19.
EID2, also known as EP300 interacting inhibitor of differentiation 2, is a human gene. EID2 may function as an endogenous suppressor of TGF-beta signaling and inhibits differentiation by blocking the histone acetyltransferase activity of p300, class I histone deacetylase, HDACs. The N-terminal portion of EID-2 was required for the binding to HDACs. This region was also involved in the transcriptional repression and nuclear localization, suggesting the importance of the involvement of HDACs in the EID-2 function. EID-2 inhibits TGF-beta/Smad transcriptional responses. EID-2 interacts constitutively with Smad proteins, and most strongly with Smad3. Stable expression of EID-2 in the TGF-beta1-responsive cell line inhibits endogenous Smad3-Smad4 complex formation and TGF-beta1-induced expression of p21 and p15. EID-2 displays developmentally regulated expression with high levels in adult heart and brain. Overexpression of EID-2 inhibits muscle-specific gene expression through inhibition of MyoD-dependent transcription. This inhibitory effect on gene expression can be explained by EID-2's ability to associate with and inhibit the acetyltransferase activity of p300.
EID2 interacts with EP300 and acts as a repressor of MYOD-dependent transcription and muscle differentiation. EID2 inhibits EP300 histone acetyltransferase activity. EID2 acts as a repressor of TGFB/SMAD transcriptional responses. EID2 may act as a repressor of the TGFB/SMAD3-dependent signaling by selectively blocking formation of TGFB-induced SMAD3-SMAD4 complex.
EID2 is also known as CRI2, EID-2.
Associated Diseases
- schizophrenia 15
- Phelan-McDermid syndrome
- early-onset non-syndromic cataract
- cataract
- Potocki-Lupski syndrome
- FRAXE intellectual disability
- hydrocephaly-cerebellar agenesis syndrome
- spinocerebellar ataxia, autosomal recessive 24
- granular corneal dystrophy type I
- hereditary hyperferritinemia with congenital cataracts
- cataract 38
- cataract 13 with adult I phenotype
- cataract 5 multiple types