E2F is a group of genes that codifies a family of
transcription factors (TF) in higher eukaryotes. Three of them are activators: E2F1,2 and E2F3a. Six others act as suppressors: E2F3b, E2F4-8. All of them are involved in the cell cycleregulation and synthesis of DNA in mammalian cells. E2Fs as TFs bind to the TTTCGCGC consensus binding sitein the target promotersequence.
Homo sapiens [http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=NM_005225.1 E2F1 mRNA] or [http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=protein&val=12669911 E2F1 protein] sequences from NCBI protein and nucleotide database.
X-ray crystallographic analysis has shown that the E2F family of transcription factors has a fold similar to the winged-helix DNA-binding motif.cite journal | author = Zheng N, Fraenkel E, Pabo CO, Pavletich NP | title = Structural basis of DNA recognition by the heterodimeric cell cycle transcription factor E2F-DP | journal = Genes Dev. | volume = 13 | issue = 6 | pages = 666–74 | year = 1999 | pmid = 10090723 | doi = 10.1101/gad.13.6.666 | url = | issn = ]
Role in the cell cycle
E2F family member play a major role during the G1/S transition in the mammalian
cell cycle(see [http://www.genome.jp/dbget-bin/show_pathway?hsa04110+1869 KEGG cell cycle pathway] ). Among E2F transcriptional targets are cyclins, cdks, checkpoints regulators, DNA repairand replication proteins.
The Rb tumour suppressor protein (pRb) binds to the E2F-1 transcription factor preventing it from interacting with the cells transcription machinery. In the absence of pRb, E2F-1 (along with its binding partner DP-1) mediates the trans-activation of E2F-1 target genes that facilitate the G1/S transition and S-phase. E2F target genes encode proteins involved in DNA replication (for example DNA polymerase, thymidine kinase (TK), dihydrofolate reductase (DHFR) and cdc6), chromosomal replication (replication origin-binding protein HsOrc1 and MCM 5). When cells are not proliferating, E2F DNA binding sites contribute to transcriptional repression. In vivo footprinting experiments obtained on
Cdc2and B-myb promoters demonstrated E2F DNA binding site occupation during G0 and early G1, when E2F is in transcriptional repressive complexes with the pocket proteins.
Activators: E2F1, E2F2, E2F3a
Activators are maximally expressed late in G1 and can be found in association with E2F regulated promoters during the G1/S transition. The activation of E2F-3a genes follows upon the
growth factorstimulation and the subsequent phosphorylationof the E2F inhibitor Retinoblastoma protein, pRB. The phosphorylationof pRB is initiated by Cyclin D/cdk4,6 complex and continued by Cyclin E/cdk2. Cyclin D/cdk4,6 itself is activated by the MAPKsignaling pathway.
When bound to E2F-3a, pRb can directly repress E2F-3a target genes by recruiting chromatin remodeling complexes and histone modifying activities (e.g. histone deacetylase,
HDAC) to the promoter.
Inhibitors: E2F3b, E2F4, E2F5, E2F6, E2F7, E2F8
* E2F3b, E2F4, E2F5 are expressed in quiescent cells and can be found associated with E2F-binding elements on E2F-target promoters during G0-phase. E2F-4 and 5 preferentially bind to p107/p130.
* E2F-6 acts as a transcriptional repressor, but through a distinct, pocket protein independent manner. E2F-6 mediates repression by direct binding to
polycomb-group proteinsor via the formation of a large multimeric complex containing Mga and Max proteins.
* E2F7 and E2F8 proteins can function as repressors independently of DP interaction. They are unique in having a duplicated conserved E2F-like DNA-binding domain and in lacking a DP1,2-dimerization domain. The exact mechanism of mediating repression is not yet understood.
* Cell cycle: CCNA1,2, CCND1,2, CDK2, MYB, E2F1,2,3, TFDP1, CDC25A
* Negative regulators: E2F7, RB1, TP107, TP21
TP53, BRCA1,2, BUB1
* Apoptosis: TP73, APAF1, CASP3,7,8, MAP3K5,14
* Nucleotide synthesis:
thymidine kinase(tk), thymidylate synthase (ts), DHFR
* DNA repair: BARD1, RAD51, UNG1,2, FANCA, FANCC, FANCJ
* DNA replication:
PCNA, histoneH2A, DNA pol and , RPA1,2,3, CDC6, MCM2,3,4,5,6,7
cite journal | author = Cobrinik D | title = Pocket proteins and cell cycle control | journal = Oncogene | volume = 24 | issue = 17 | pages = 2796–809 | year = 2005 | pmid = 15838516 | doi = 10.1038/sj.onc.1208619 | issn = ] cite journal | author = Maiti B, Li J, de Bruin A, Gordon F, Timmers C, Opavsky R, Patil K, Tuttle J, Cleghorn W, Leone G | title = Cloning and characterization of mouse E2F8, a novel mammalian E2F family member capable of blocking cellular proliferation | journal = J. Biol. Chem. | volume = 280 | issue = 18 | pages = 18211–20 | year = 2005 | pmid = 15722552 | doi = 10.1074/jbc.M501410200 | issn = ] cite journal | author = Ogawa H, Ishiguro K, Gaubatz S, Livingston DM, Nakatani Y | title = A complex with chromatin modifiers that occupies E2F- and Myc-responsive genes in G0 cells | journal = Science | volume = 296 | issue = 5570 | pages = 1132–6 | year = 2002 | pmid = 12004135 | doi = 10.1126/science.1069861 | issn = ] cite journal | author = Tommasi S, Pfeifer GP | title = In vivo structure of the human cdc2 promoter: release of a p130-E2F-4 complex from sequences immediately upstream of the transcription initiation site coincides with induction of cdc2 expression | journal = Mol. Cell. Biol. | volume = 15 | issue = 12 | pages = 6901–13 | year = 1995 | pmid = 8524257 | doi = | issn = | url = http://mcb.asm.org/cgi/content/abstract/15/12/6901 | format = abstract ] cite journal | author = Zwicker J, Liu N, Engeland K, Lucibello FC, Müller R | title = Cell cycle regulation of E2F site occupation in vivo | journal = Science | volume = 271 | issue = 5255 | pages = 1595–7 | year = 1996 | pmid = 8599118 | doi = 10.1126/science.271.5255.1595 | issn = ] cite journal | author = Tategu M, Arauchi T,Tanaka R,Nakagawa H, Yoshida K | title = Systems Biology-Based Identifi cation of Crosstalk between E2F Transcription Factors and the Fanconi Anemia Pathway | journal = Gene Regulation and Systems Biology | volume = 1 | issue = 1 | pages = 1–7 | year = 2007 | pmid = | doi = | issn = | url = http://la-press.com/article.php?article_id=219 ]
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