- E6 - protein
The E6 protein is one of the key cancer-causing proteins expressed by the
Human papillomavirus(HPV). Among the strains of HPV known to cause physical changes associated with cancer and pre-cancerous lesions, three oncoproteins are recognized: E5, E6 and E7. Although low-risk HPV strains also produce these proteins, the four major high-risk strains—HPV-16, HPV-18, HPV-31, and HPV-45—all exhibit E6 and E7 proteins.cite journal |author=Gupta S, Takhar PP, Degenkolbe R, Koh CH, Zimmermann H, Yang CM, Guan Sim K, Hsu SI, Bernard HU |title=The human papillomavirus type 11 and 16 E6 proteins modulate the cell-cycle regulator and transcription cofactor TRIP-Br1 |journal=Virology |volume=317 |issue=1 |pages=155–64 |year=2003 |url=http://www.gis.nus.edu.sg/homepage/upload%5Cpublications%5C1012.pdf |pmid=14675634 |doi=10.1016/j.virol.2003.08.008 |format=dead link|date=June 2008 – [http://scholar.google.co.uk/scholar?hl=en&lr=&q=author%3A+intitle%3AThe+human+papillomavirus+type+11+and+16+E6+proteins+modulate+the+cell-cycle+regulator+and+transcription+cofactor+TRIP-Br1&as_publication=Virology&as_ylo=2003&as_yhi=2003&btnG=Search Scholar search] ] E6's activity in the high-risk strains can be oncogenic, or cancer-promoting. Therefore, it is the strains which exhibit these proteins which are associated with cervical cancerand pre-cancerous lesion development in women.
tructure of E6
E6 is a 151 amino-acid peptide that incorporates a type 1 motif with a
consensus sequence–(T/S)-(X)-(V/I)-COOH.cite journal |author=Glaunsinger BA, Lee SS, Thomas M, Banks L, Javier R |title=Interactions of the PDZ-protein MAGI-1 with adenovirus E4-ORF1 and high-risk papillomavirus E6 oncoproteins |journal=Oncogene |volume=19 |issue=46 |pages=5270–80 |year=2000 |url=http://www.nature.com/onc/journal/v19/n46/full/1203906a.html |pmid=11077444 |doi=10.1038/sj.onc.1203906] It also has two zinc fingermotifs.
E6 is of particular interest because it appears to have multiple roles in the cell and to interact with many other proteins. E6 primarily causes cancer by associating with and thereby inactivating
P53or Rb proteins, which act as tumor suppressors. When tumor suppressor proteins are inactivated tumor growth proceeds unchecked. E6's interaction with p53 and Rb marks these proteins for degradation by ubiquitylationand ubiquitin ligase. [cite web |url=http://www.ihop-net.org/UniPub/iHOP/gs/92974.html |title=iHOP information Hyperlinked over Proteins UBE3A |accessdate=2007-05-01] [cite web |url=http://www.nottingham.ac.uk/biochemcourses/students/ub/ubenz.html |title=Biochemistry, Nottingham University - 3.0 Enzymes of the Ubiquitin Pathway |accessdate=2007-05-01] E6 is proven to act on other cellular proteins, and to positively affect telomeraseactivity, thus inactivating one of the ways by which cells are normally prevented from dividing unchecked. [cite journal |author=Kelley ML, Keiger KE, Lee CJ, Huibregtse JM |title=The global transcriptional effects of the human papillomavirus E6 protein in cervical carcinoma cell lines are mediated by the E6AP ubiquitin ligase |journal=J. Virol. |volume=79 |issue=6 |pages=3737–47 |year=2005 |url=http://jvi.asm.org/cgi/content/abstract/79/6/3737 |pmid=15731267 |doi=10.1128/JVI.79.6.3737-3747.2005] Additionally, E6 can act as a transcriptional cofactor—specifically, a transcription activator—when interacting with the cellular transcription factor, E2F1/DP1.
E6 can also bind to PDZ-domains, short sequences which are often found in signalling proteins. E6's structural motif allows for interaction with PDZ domains on DLG (discs large) and hDLG (Drosophila large) tumor suppressor genes.cite journal |author=Kiyono T, Hiraiwa A, Fujita M, Hayashi Y, Akiyama T, Ishibashi M |title=Binding of high-risk human papillomavirus E6 oncoproteins to the human homologue of the Drosophila discs large tumor suppressor protein |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=94 |issue=21 |pages=11612–6 |year=1997 |url=http://www.pnas.org/cgi/content/full/94/21/11612#abs |pmid=9326658 |doi=10.1073/pnas.94.21.11612] Binding at these locations causes transformation of the DLG protein and disruption of its suppressor function. E6 proteins also interact with the MAGUK (membrane-associated guanylate kinase family) proteins. These proteins, including MAGI-1, MAGI-2, and MAGI-3 are usually structural proteins, and can help with signaling. More significantly, they are believed to be involved with DLG's suppression activity. When E6 complexes with the PDZ domains on the MAGI proteins, it distorts their shape and thereby impedes their function. Overall, the E6 protein serves to impede normal protein activity in such a way as to allow a cell to grow and multiply at the increased rate characteristic of cancer.
Wikimedia Foundation. 2010.