E2F1 Available structures PDB Ortholog search: PDBe RCSB
Identifiers Aliases E2F1 , E2F-1, RBAP1, RBBP3, RBP3, E2F transcription factor 1External IDs OMIM : 189971 MGI : 101941 HomoloGene : 3828 GeneCards : E2F1 show Gene location (Human )Chr. Chromosome 20 (human) [1] Band 20q11.22 Start 33,675,477 bp [1] End 33,686,385 bp [1]
show Gene location (Mouse )Chr. Chromosome 2 (mouse)[2] Band 2 H1|2 76.79 cM Start 154,559,407 bp [2] End 154,569,892 bp [2]
show Gene ontology Molecular function • DNA binding • GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity • transcription factor binding • GO:0001948 protein binding • protein dimerization activity • GO:0001078, GO:0001214, GO:0001206 DNA-binding transcription repressor activity, RNA polymerase II-specific • sequence-specific DNA binding • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific • protein kinase binding • GO:0001158 cis-regulatory region sequence-specific DNA binding • GO:0001077, GO:0001212, GO:0001213, GO:0001211, GO:0001205 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 Ensembl UniProt RefSeq (mRNA) RefSeq (protein) Location (UCSC) Chr 20: 33.68 – 33.69 Mb Chr 2: 154.56 – 154.57 Mb PubMed search[3] [4] Wikidata
Transcription factor E2F1 is a protein that in humans is encoded by the E2F1 gene .[5]
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 .[6]
Transcription [ ]
E2F1 promoter[PAX8] => E2F1 PMID 21602887
Interactions [ ]
E2F1 has been shown to interact with:
ARID3A ,[7]
CUL1 ,[8]
Cyclin A1 ,[9]
Cyclin A2 ,[10]
GTF2H1 ,[11]
MDM4 ,[12]
NCOA6 ,[13]
NDN ,[14] [15]
NPDC1 ,[16]
PURA ,[17]
PHB ,[18] [19] [20] [21]
RB1 ,[14] [22] [23] [24] [25] [26] [27]
RBL1 ,[22]
SKP2 ,[8]
SP1 ,[28] [29] [30]
SP2 ,[28]
SP3 ,[28]
SP4 ,[28]
TFDP1 [7] [27] [31] [32]
TOPBP1 ,[33] [34]
TP53BP1 ,[25] and
UBC .[35]
See also [ ]
References [ ]
^ Jump up to: a b c GRCh38: Ensembl release 89: ENSG00000101412 - Ensembl , May 2017
^ Jump up to: a b c GRCm38: Ensembl release 89: ENSMUSG00000027490 - Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Neuman E, Sellers WR, McNeil JA, Lawrence JB, Kaelin WG (December 1996). "Structure and partial genomic sequence of the human E2F1 gene". Gene . 173 (2): 163–9. doi :10.1016/0378-1119(96)00184-9 . PMID 8964493 .
^ "Entrez Gene: E2F1 E2F transcription factor 1" .
^ Jump up to: a b 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 .
^ Jump up to: a b 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 .
^ 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 .
^ 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 .
^ 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 .
^ 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 .
^ Kong HJ, Yu HJ, Hong S, Park MJ, Choi YH, An WG, Lee JW, Cheong J (November 2003). "Interaction and functional cooperation of the cancer-amplified transcriptional coactivator activating signal cointegrator-2 and E2F-1 in cell proliferation". Mol. Cancer Res . 1 (13): 948–58. PMID 14638867 .
^ Jump up to: a b Taniura H, Taniguchi N, Hara M, Yoshikawa K (January 1998). "Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2F1" . J. Biol. Chem . 273 (2): 720–8. doi :10.1074/jbc.273.2.720 . PMID 9422723 .
^ 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 .
^ 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 .
^ 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 .
^ 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 .
^ 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 .
^ 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 .
^ 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 .
^ Jump up to: a b 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 .
^ 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 .
^ 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 .
^ Jump up to: a b 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 .
^ Fajas L, Paul C, Zugasti O, Le Cam L, Polanowska J, Fabbrizio E, Medema R, Vignais ML, Sardet C (July 2000). "pRB binds to and modulates the transrepressing activity of the E1A-regulated transcription factor p120E4F" . Proc. Natl. Acad. Sci. U.S.A . 97 (14): 7738–43. Bibcode :2000PNAS...97.7738F . doi :10.1073/pnas.130198397 . PMC 16614 . PMID 10869426 .
^ Jump up to: a b Wu CL, Zukerberg LR, Ngwu C, Harlow E, Lees JA (May 1995). "In vivo association of E2F and DP family proteins" . Mol. Cell. Biol . 15 (5): 2536–46. doi :10.1128/mcb.15.5.2536 . PMC 230484 . PMID 7739537 .
^ Jump up to: a b c d Rotheneder H, Geymayer S, Haidweger E (November 1999). "Transcription factors of the Sp1 family: interaction with E2F and regulation of the murine thymidine kinase promoter". J. Mol. Biol . 293 (5): 1005–15. doi :10.1006/jmbi.1999.3213 . PMID 10547281 .
^ Lin SY, Black AR, Kostic D, Pajovic S, Hoover CN, Azizkhan JC (April 1996). "Cell cycle-regulated association of E2F1 and Sp1 is related to their functional interaction" . Mol. Cell. Biol . 16 (4): 1668–75. doi :10.1128/MCB.16.4.1668 . PMC 231153 . PMID 8657142 .
^ Karlseder J , Rotheneder H, Wintersberger E (April 1996). "Interaction of Sp1 with the growth- and cell cycle-regulated transcription factor E2F" . Mol. Cell. Biol . 16 (4): 1659–67. doi :10.1128/mcb.16.4.1659 . PMC 231152 . PMID 8657141 .
^ 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 .
^ 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 .
^ 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 .
^ 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 .
^ 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). "[Identification of NPDC-1, gene involved in the control of proliferation and differentiation of neural and glial precursors]". 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. 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 [ ]
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2aze : Structure of the Rb C-terminal domain bound to an E2F1-DP1 heterodimer
This article incorporates text from the United States National Library of Medicine , which is in the public domain .