Skip NavigationSkip to Content

Analysis of the Interaction Between Human Papillomavirus Type 16 E7 and the Tata Binding Protein, Tbp

  1. Author:
    Phillips, A. C.
    Vousden, K. H.
  2. Author Address

    Vousden KH NCI FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM W 7TH ST FREDERICK, MD 21701 USA NCI FREDERICK CANC RES & DEV CTR ABL BASIC RES PROGRAM FREDERICK, MD 21701 USA
    1. Year: 1997
  1. Journal: Journal of General Virology
    1. 78
    2. Part 4
    3. Pages: 905-909
  2. Type of Article: Article
  1. Abstract:

    The E7 protein encoded by human papillomavirus type 16 shows transforming and immortalizing activities which are mediated, in part, through the interaction of the viral oncoprotein with the pRB protein family, This interaction is not solely responsible for E7 function, however, and other properties of E7, such as the interaction with basal transcription factors such as TBP, are likely to be of importance. We show here that three regions of the viral protein contribute to the interaction between E7 and TBP; the pRB-binding domain, the casein kinase II phosphorylation region and the C-terminal dimerization domain. Mutations within each region reduced the interaction of E7 with TBP in vitro, and simultaneous alterations within each of these regions completely abrogated binding, Unlike the pRB interaction, the association of E7 with TBP was enhanced following phosphorylation of E7 by casein kinase II, demonstrating a functional significance for phosphorylation of the viral protein. [References: 25]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel