Biology:E2F4

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Transcription factor E2F4 is a protein that in humans is encoded by the E2F4 gene.[1][2]

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. This protein binds to all three of the tumor suppressor proteins pRB, p107 and p130, but with higher affinity to the last two. It plays an important role in the suppression of proliferation-associated genes, and its gene mutation and increased expression may be associated with human cancer.[3]

Structure

The E2F proteins contain several evolutionally 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 (Asp + Glu), and a tumor suppressor protein association domain which is embedded within the transactivation domain.

Interactions

E2F4 has been shown to interact with Smad3.[4]

See also

References

  1. "E2F-4, a new member of the E2F transcription factor family, interacts with p107". Genes Dev 8 (22): 2665–79. Dec 1994. doi:10.1101/gad.8.22.2665. PMID 7958924. 
  2. "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. Apr 1995. doi:10.1073/pnas.92.6.2403. PMID 7892279. Bibcode1995PNAS...92.2403S. 
  3. "Entrez Gene: E2F4 E2F transcription factor 4, p107/p130-binding". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1874. 
  4. "E2F4/5 and p107 as Smad cofactors linking the TGFbeta receptor to c-myc repression". Cell 110 (1): 19–32. July 2002. doi:10.1016/S0092-8674(02)00801-2. PMID 12150994. 

Further reading

External links

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