Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:Q15744 (
C/EBP epsilon
)
82
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Neutrophils from CCAAT enhancer binding protein epsilon (
C/EBP epsilon
) knockout mice have morphological and biochemical features similar to those observed in patients with an extremely rare
congenital disorder
called neutrophil-specific secondary granule deficiency (SGD). SGD is characterized by frequent bacterial infections attributed, in part, to the lack of neutrophil secondary granule proteins (SGP). A mutation that results in loss of functional
C/EBP epsilon
activity has recently been described in an SGD patient, and has been postulated to be the cause of the disease in this patient. We have previously demonstrated that overexpression of CCAAT displacement protein (CDP/cut), a highly conserved transcriptional repressor of developmentally regulated genes, suppresses expression of SGP genes in 32Dcl3 cells. This phenotype resembles that observed in both
C/EBP epsilon
(-/-) mice and in SGD patients. Based on these observations we investigated potential interactions between
C/EBP epsilon
and CDP/cut during neutrophil maturation. In this study, we demonstrate that inducible expression of
C/EBP epsilon
in 32Dcl3/tet cells results in granulocytic differentiation. Furthermore, Northern blot analysis of G-CSF-induced CDP/cut overexpressing 32Dcl3 cells revealed absence of
C/EBP epsilon
mRNA. We therefore hypothesize that
C/EBP epsilon
positively regulates SGP gene expression, and that
C/EBP epsilon
is itself negatively regulated by CDP/cut during neutrophil maturation. We further demonstrate that the
C/EBP epsilon
promoter is regulated by CDP/cut during myeloid differentiation.
...
PMID:C/EBP epsilon mediates myeloid differentiation and is regulated by the CCAAT displacement protein (CDP/cut). 1143 45