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E2F1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1H24, 1O9K, 2AZE
Identifiers
Aliases	E2F1, E2F-1, RBAP1, RBBP3, RBP3, E2F transcription factor 1
External IDs	OMIM: 189971; MGI: 101941; HomoloGene: 3828; GeneCards: E2F1; OMA:E2F1 - orthologs
Gene location (Human) Chr. Chromosome 20 (human) Band 20q11.22 Start 33,675,477 bp End 33,686,385 bp
Gene location (Mouse) Chr. Chromosome 2 (mouse) Band 2 H1|2 76.79 cM Start 154,401,327 bp End 154,411,812 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in ganglionic eminence secondary oocyte ventricular zone gonad mucosa of transverse colon stromal cell of endometrium prefrontal cortex testicle bone marrow putamen Top expressed in zygote secondary oocyte ectoderm otic vesicle otic placode primary oocyte fetal liver hematopoietic progenitor cell ventricular zone saccule gastrula More reference expression data BioGPS More reference expression data
Gene ontology Molecular function DNA binding DNA-binding transcription factor activity transcription factor binding protein binding protein dimerization activity DNA-binding transcription repressor activity, RNA polymerase II-specific sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific protein kinase binding cis-regulatory region sequence-specific DNA binding DNA-binding transcription activator activity, RNA polymerase II-specific Cellular component cytoplasm transcription regulator complex Rb-E2F complex nucleus mitochondrion nucleoplasm centrosome protein-containing complex RNA polymerase II transcription regulator complex Biological process cellular response to nerve growth factor stimulus negative regulation of fat cell differentiation regulation of transcription, DNA-templated lens fiber cell apoptotic process negative regulation of transcription involved in G1/S transition of mitotic cell cycle positive regulation of fibroblast proliferation negative regulation of DNA binding negative regulation of fat cell proliferation DNA damage checkpoint signaling cellular response to xenobiotic stimulus negative regulation of transcription by RNA polymerase II transcription, DNA-templated regulation of cell cycle positive regulation of transcription, DNA-templated regulation of G1/S transition of mitotic cell cycle mRNA stabilization positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway positive regulation of gene expression cellular response to fatty acid anoikis spermatogenesis intrinsic apoptotic signaling pathway in response to DNA damage intrinsic apoptotic signaling pathway by p53 class mediator cell cycle forebrain development negative regulation of transcription, DNA-templated cellular response to hypoxia positive regulation of transcription by RNA polymerase II apoptotic process DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest regulation of transcription involved in G1/S transition of mitotic cell cycle positive regulation of apoptotic process negative regulation of G0 to G1 transition positive regulation of glial cell proliferation Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 1869 13555 Ensembl ENSG00000101412 ENSMUSG00000027490 UniProt Q01094 Q61501 RefSeq (mRNA) NM_005225 NM_007891 NM_001291105 RefSeq (protein) NP_005216 NP_001278034 NP_031917 Location (UCSC) Chr 20: 33.68 – 33.69 Mb Chr 2: 154.4 – 154.41 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Transcription factor E2F1 is a protein that in humans is encoded by the E2F1 gene.

Function

The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionarily conserved domains found in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein and another 2 members, E2F2 and E2F3, have an additional cyclin binding domain. This protein binds preferentially to retinoblastoma protein pRB in a cell-cycle dependent manner. It can mediate both cell proliferation and p53-dependent/independent apoptosis.

Transcription

E2F1 promoter => E2F1

Interactions

E2F1 has been shown to interact with:

• ARID3A,
• CUL1,
• Cyclin A1,
• Cyclin A2,
• GTF2H1,
• MDM4,
• NCOA6,
• NDN,
• NPDC1,
• PURA,
• PHB,
• RB1,
• UDG,
• RBL1,
• SKP2,
• SP1,
• SP2,
• SP3,
• SP4,
• TFDP1
• TOPBP1,
• TP53BP1, and
• UBC.

See also

• E2F
• Retinoblastoma protein

References

1. ^ GRCh38: Ensembl release 89: ENSG00000101412 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000027490 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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6. "Entrez Gene: E2F1 E2F transcription factor 1".
7. Li CG, Nyman JE, Braithwaite AW, Eccles MR (December 2011). "PAX8 promotes tumor cell growth by transcriptionally regulating E2F1 and stabilizing RB protein". Oncogene. 30 (48): 4824–34. doi:10.1038/onc.2011.190. PMC 3229668. PMID 21602887.
8. ^ Suzuki M, Okuyama S, Okamoto S, Shirasuna K, Nakajima T, Hachiya T, Nojima H, Sekiya S, Oda K (August 1998). "A novel E2F binding protein with Myc-type HLH motif stimulates E2F-dependent transcription by forming a heterodimer". Oncogene. 17 (7): 853–65. doi:10.1038/sj.onc.1202163. PMID 9780002.
9. ^ Marti A, Wirbelauer C, Scheffner M, Krek W (May 1999). "Interaction between ubiquitin-protein ligase SCFSKP2 and E2F-1 underlies the regulation of E2F-1 degradation". Nat. Cell Biol. 1 (1): 14–9. doi:10.1038/8984. PMID 10559858. S2CID 8884226.
10. Yang R, Müller C, Huynh V, Fung YK, Yee AS, Koeffler HP (March 1999). "Functions of cyclin A1 in the cell cycle and its interactions with transcription factor E2F-1 and the Rb family of proteins". Mol. Cell. Biol. 19 (3): 2400–7. doi:10.1128/mcb.19.3.2400. PMC 84032. PMID 10022926.
11. Xu M, Sheppard KA, Peng CY, Yee AS, Piwnica-Worms H (December 1994). "Cyclin A/CDK2 binds directly to E2F-1 and inhibits the DNA-binding activity of E2F-1/DP-1 by phosphorylation". Mol. Cell. Biol. 14 (12): 8420–31. doi:10.1128/MCB.14.12.8420. PMC 359381. PMID 7969176.
12. Vandel L, Kouzarides T (August 1999). "Residues phosphorylated by TFIIH are required for E2F-1 degradation during S-phase". EMBO J. 18 (15): 4280–91. doi:10.1093/emboj/18.15.4280. PMC 1171504. PMID 10428966.
13. Strachan GD, Jordan-Sciutto KL, Rallapalli R, Tuan RS, Hall DJ (February 2003). "The E2F-1 transcription factor is negatively regulated by its interaction with the MDMX protein". J. Cell. Biochem. 88 (3): 557–68. doi:10.1002/jcb.10318. PMID 12532331. S2CID 38805122.
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16. Kuwako K, Taniura H, Yoshikawa K (January 2004). "Necdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptor". J. Biol. Chem. 279 (3): 1703–12. doi:10.1074/jbc.M308454200. PMID 14593116.
17. Sansal I, Dupont E, Toru D, Evrard C, Rouget P (October 2000). "NPDC-1, a regulator of neural cell proliferation and differentiation, interacts with E2F-1, reduces its binding to DNA and modulates its transcriptional activity". Oncogene. 19 (43): 5000–9. doi:10.1038/sj.onc.1203843. PMID 11042687.
18. Darbinian N, Gallia GL, Kundu M, Shcherbik N, Tretiakova A, Giordano A, Khalili K (November 1999). "Association of Pur alpha and E2F-1 suppresses transcriptional activity of E2F-1". Oncogene. 18 (46): 6398–402. doi:10.1038/sj.onc.1203011. PMID 10597240.
19. Joshi B, Ko D, Ordonez-Ercan D, Chellappan SP (December 2003). "A putative coiled-coil domain of prohibitin is sufficient to repress E2F1-mediated transcription and induce apoptosis". Biochem. Biophys. Res. Commun. 312 (2): 459–66. doi:10.1016/j.bbrc.2003.10.148. PMID 14637159.
20. Fusaro G, Dasgupta P, Rastogi S, Joshi B, Chellappan S (November 2003). "Prohibitin induces the transcriptional activity of p53 and is exported from the nucleus upon apoptotic signaling". J. Biol. Chem. 278 (48): 47853–61. doi:10.1074/jbc.M305171200. PMID 14500729.
21. Wang S, Zhang B, Faller DV (June 2002). "Prohibitin requires Brg-1 and Brm for the repression of E2F and cell growth". EMBO J. 21 (12): 3019–28. doi:10.1093/emboj/cdf302. PMC 126057. PMID 12065415.
22. Wang S, Nath N, Fusaro G, Chellappan S (November 1999). "Rb and prohibitin target distinct regions of E2F1 for repression and respond to different upstream signals". Mol. Cell. Biol. 19 (11): 7447–60. doi:10.1128/mcb.19.11.7447. PMC 84738. PMID 10523633.
23. ^ Dyson N, Dembski M, Fattaey A, Ngwu C, Ewen M, Helin K (December 1993). "Analysis of p107-associated proteins: p107 associates with a form of E2F that differs from pRB-associated E2F-1". J. Virol. 67 (12): 7641–7. doi:10.1128/JVI.67.12.7641-7647.1993. PMC 238233. PMID 8230483.
24. Nicolas E, Ait-Si-Ali S, Trouche D (August 2001). "The histone deacetylase HDAC3 targets RbAp48 to the retinoblastoma protein". Nucleic Acids Res. 29 (15): 3131–6. doi:10.1093/nar/29.15.3131. PMC 55834. PMID 11470869.
25. Pardo PS, Leung JK, Lucchesi JC, Pereira-Smith OM (December 2002). "MRG15, a novel chromodomain protein, is present in two distinct multiprotein complexes involved in transcriptional activation". J. Biol. Chem. 277 (52): 50860–6. doi:10.1074/jbc.M203839200. PMID 12397079.
26. ^ Choubey D, Li SJ, Datta B, Gutterman JU, Lengyel P (October 1996). "Inhibition of E2F-mediated transcription by p202". EMBO J. 15 (20): 5668–78. doi:10.1002/j.1460-2075.1996.tb00951.x. PMC 452311. PMID 8896460.
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33. Sardet C, Vidal M, Cobrinik D, Geng Y, Onufryk C, Chen A, Weinberg RA (March 1995). "E2F-4 and E2F-5, two members of the E2F family, are expressed in the early phases of the cell cycle". Proc. Natl. Acad. Sci. U.S.A. 92 (6): 2403–7. Bibcode:1995PNAS...92.2403S. doi:10.1073/pnas.92.6.2403. PMC 42492. PMID 7892279.
34. Helin K, Wu CL, Fattaey AR, Lees JA, Dynlacht BD, Ngwu C, Harlow E (October 1993). "Heterodimerization of the transcription factors E2F-1 and DP-1 leads to cooperative trans-activation". Genes Dev. 7 (10): 1850–61. doi:10.1101/gad.7.10.1850. PMID 8405995.
35. Liu K, Lin FT, Ruppert JM, Lin WC (May 2003). "Regulation of E2F1 by BRCT domain-containing protein TopBP1". Mol. Cell. Biol. 23 (9): 3287–304. doi:10.1128/mcb.23.9.3287-3304.2003. PMC 153207. PMID 12697828.
36. Yu X, Chini CC, He M, Mer G, Chen J (October 2003). "The BRCT domain is a phospho-protein binding domain". Science. 302 (5645): 639–42. Bibcode:2003Sci...302..639Y. doi:10.1126/science.1088753. PMID 14576433. S2CID 29407635.
37. Zhou F, Zhang L, Wang A, Song B, Gong K, Zhang L, Hu M, Zhang X, Zhao N, Gong Y (May 2008). "The association of GSK3 beta with E2F1 facilitates nerve growth factor-induced neural cell differentiation". J. Biol. Chem. 283 (21): 14506–15. doi:10.1074/jbc.M706136200. PMID 18367454.

Further reading

• Dupont E, Sansal I, Toru D, Evrard C, Rouget P (1997). "". C. R. Séances Soc. Biol. Fil. 191 (1): 95–104. PMID 9181131.
• Stevens C, La Thangue NB (2005). "The emerging role of E2F-1 in the DNA damage response and checkpoint control". DNA Repair (Amst.). 3 (8–9): 1071–9. doi:10.1016/j.dnarep.2004.03.034. PMID 15279795.
• Zhang Z, Wang H, Li M, Rayburn E, Agrawal S, Zhang R (2006). "Novel MDM2 p53-independent functions identified through RNA silencing technologies". Ann. N. Y. Acad. Sci. 1058 (1): 205–14. Bibcode:2005NYASA1058..205Z. doi:10.1196/annals.1359.030. PMID 16394138. S2CID 35683657.
• Schild C, Wirth M, Reichert M, Schmid RM, Saur D, Schneider G (July 2009). "PI3K signaling maintains c-myc expression to regulate transcription of E2F1 in pancreatic cancer cells". Mol. Carcinog. 48 (12): 1149–58. doi:10.1002/mc.20569. PMID 19603422. S2CID 41545085.

External links

• E2F1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
• FactorBook E2F1

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

• Genes on human chromosome 20
• Transcription factors