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E2F3 — E2F4

Pathways - manually collected, often from reviews:

• FastForward regulation: E2F4 → E2F3 (transcriptional regulation, unknown) Cam et al., Mol Cell 2004
  Evidence: DNABINDING
• NCI Pathway Database E2F transcription factor network: E2F1-3/DP complex (E2F3_E2F2_E2F1-TFDP1) → E2F4/DP2/p107-p130 complex (E2F4-RBL2_RBL1-TFDP2) (transcription, activates)
  Takahashi et al., Genes Dev 2000, Zhu et al., EMBO J 2004, Hurford et al., Genes Dev 1997
  Evidence: mutant phenotype, reporter gene, physical interaction
• NCI Pathway Database E2F transcription factor network: CEBPA/BRM/RB1/E2F4 complex (CEBPA-SMARCA2-RB1-E2F4) → E2F1-3/DP complex (E2F3_E2F2_E2F1-TFDP1) (transcription, inhibits)
  Iakova et al., Cell 2003, Hiebert et al., Proc Natl Acad Sci U S A 1989
  Evidence: mutant phenotype, reporter gene, physical interaction

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

Studies that report less than 10 interactions are marked with *

• Gene Ontology Complexes transcription factor complex: transcription factor complex complex (ATF7IP-GSC-GCM1-MAFB-NKX2-1-NKX2-5-RARG-KLF4-FOXF1-FOXF2-FOXE3-LDB1-ZFHX3-GATA6-SNAI3-FOXH1-KAT5-AHR-EYA3-NFATC2-CRX-MED27-HES6-SKI-XRCC6-ARNTL-SUB1-JUN-SOX17-SCX-DMBX1-TCF4-TCF7-PDLIM1-TFEB-LBX1-TRRAP-NAA16-EPAS1-MGA-PTF1A-HOXD12-MEF2B-TFDP3-TFDP1-HDAC2-YY1-SMAD9-CLOCK-ONECUT3-SMAD5-SMAD6-SMAD7-SMAD1-SMAD2-PRKDC-RCOR2-NHLH2-REL-TBX5-ARNTL2-BSX-HOXA10-HOXB13-MED23-PUS1-TAL1-RBL1-RBL2-MINA-HMGA1-BARX2-LEF1-EP300-PMF1-ARID5A-WWTR1-LMO2-LMO4-TP73-ABT1-CDK2-DKFZp686M216-CREG1-CTNNB1-SOX9-HAND2-SOX2-TEAD2-MYOG-TEAD4-CEBPA-GFI1B-MYOD1-ALX1-NPAS4-TFAP2D-FIGLA-ALX4-ETS1-PROP1-ASCL3-HCLS1-MSX1-MSX2-SRA1-AJUBA-MTA2-SIN3A-POU3F2-POU3F1-BEX1-MLXIPL-NR2E3-PBX2-ANKRD1-E2F6-E2F5-E2F4-E2F3-E2F2-E2F1-E2F8-CREBBP-ATF5-ATF4-POU2F3) Kaspar et al., J Biol Chem 1999, Wang et al., J Biol Chem 1999, Nagpal et al., J Biol Chem 1999, Blixt et al., Genes Dev 2000, Carlberg et al., Mol Cell Biol Res Commun 2000, Bae et al., Development 2000, Cairo et al., Hum Mol Genet 2001, Tutter et al., Genes Dev 2001, Willis et al., J Biol Chem 2002, Bayne et al., Mol Hum Reprod 2004, Schubert et al., J Biol Chem 2004, Han et al., J Mol Biol 2005, Rodriguez et al., EMBO J 2005, Han et al., Nucleic Acids Res 2005, Zhang et al., Mol Cell Biol 2007, Wong et al., Cell 2009, Stevens et al., Immunology 2009, Stefanovic et al., J Cell Biol 2009, Skokowa et al., Nat Med 2012, Ge et al., Cell 1994, Durocher et al., EMBO J 1997, Hogenesch et al., Proc Natl Acad Sci U S A 1998, Hellqvist et al., J Biol Chem 1998, Ryu et al., Nature 1999
• STRING interaction: E2F3 — E2F4 (interaction, mapped from kegg_pathways)
• STRING interaction: E2F4 — E2F3 (interaction, mapped from kegg_pathways)

Text-mined interactions from Literome

Smith et al., J Biol Chem 2000 : The postconfluent dividing cells share features with cells that normally exit the cell cycle ; p27 ( kip1 ) is increased , p21 ( waf1/cip1 ) is decreased, free E2F DNA binding activity is reduced, and E2F4 is primarily nuclear
Hyde et al., Invest Ophthalmol Vis Sci 2002 : Although in the normal lens there do not appear to be unique roles for E2F1 that can not be fulfilled by other E2F family members, in the absence of functional pRB proteins, E2F1 is specifically responsible for the increased expression of E2F3a and p19ARF
Asp et al., Genes Dev 2009 : However, the role , if any, of E2F proteins, and in particular E2f3 , in myogenic differentiation is not well understood
Dingar et al., J Mol Cell Cardiol 2012 : As analyzed by chromatin immunoprecipitation, the E2F4-p130-repressor directly blocks transcription of essential apoptosis related genes, E2F1 , Apaf-1, and p73a through recruitment of histone deacetylase 1 (HDAC1)