Gene interactions and pathways from curated databases and text-mining

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CEBPA — JUN

Pathways - manually collected, often from reviews:

  • BioCarta keratinocyte differentiation: c/EBP-alpha (CEBPA) → SP1/c-FOS/c-JUN/ETS/c/EBP-alpha complex (SP1-FOS-JUN-ETS2_ETS1-CEBPA) (modification, collaborate)
  • BioCarta keratinocyte differentiation: c/EBP-alpha (CEBPA) → AP-1 complex (FOS-JUN) (modification, collaborate)
  • BioCarta keratinocyte differentiation: SP1 → SP1/c-FOS/c-JUN/ETS/c/EBP-alpha complex (SP1-FOS-JUN-ETS2_ETS1-CEBPA) (modification, collaborate)
  • BioCarta keratinocyte differentiation: HOXA7 → SP1/c-FOS/c-JUN/ETS/c/EBP-alpha complex (SP1-FOS-JUN-ETS2_ETS1-CEBPA) (modification, inhibits)
  • BioCarta keratinocyte differentiation: SP1/c-FOS/c-JUN/ETS/c/EBP-alpha complex (SP1-FOS-JUN-ETS2_ETS1-CEBPA) → AP-1 complex (FOS-JUN) (modification, collaborate)
  • BioCarta keratinocyte differentiation: SP1/c-FOS/c-JUN/ETS/c/EBP-alpha complex (SP1-FOS-JUN-ETS2_ETS1-CEBPA) → ETS (ETS2/ETS1) (modification, collaborate)

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Rangatia et al., Mol Cell Biol 2002 : An ectopic increase of C/EBPalpha expression decreases the c-Jun mRNA level, and the human c-Jun promoter activity is downregulated eightfold in the presence of C/EBPalpha ... C/EBPalpha and c-Jun interact through their leucine zipper domains, and this interaction prevents c-Jun from binding to DNA
Liu et al., Blood 2003 : C/EBPalpha-ER strongly inhibited endogenous AP-1 DNA binding
Kim et al., Exp Mol Med 2002 : C/EBP binding activity to site F of the rat GLUT2 glucose transporter gene promoter is attenuated by c-Jun in vitro
Rangatia et al., Oncogene 2003 (Leukemia, Myeloid, Acute) : Elevated c-Jun expression in acute myeloid leukemias inhibits C/EBPalpha DNA binding via leucine zipper domain interaction
Gagliardi et al., J Biol Chem 2003 : C/EBP inhibition enhanced the expression of the three major components of AP-1 in cycling CEF, namely c-Jun, JunD, and Fra-2, and stimulated AP-1 activity
Friedman et al., Blood Cells Mol Dis 2003 : In 32DPKCdelta cells, C/EBPalpha-ER strongly inhibits endogenous or exogenous JunB induction, dependent upon the outer surface of the C/EBPalpha basic region, but does not inhibit c-Jun , PU.1, or C/EBPbeta expression
Hong et al., J Leukoc Biol 2011 : C/EBPa : AP-1 heterodimers bound either site preferentially in a gel-shift assay, C/EBPa : c-Fos ER fusion proteins induced endogenous Fosb mRNA but not in the presence of CHX, C/EBP and AP-1 proteins bound the endogenous Fosb promoter, mutation of the -56 cis element reduced reporter activity fivefold, and endogenous FosB protein was expressed preferentially during monopoiesis versus granulopoiesis
Lee et al., J Cell Biochem 2012 (Insulin Resistance...) : In addition, attempts to elucidate a possible mechanism underlying the artemisinic acid mediated effects revealed that reduced expression of the C/EBP d gene was mediated by inhibiting Jun N-terminal kinase (JNK)