Two Patches of Amino Acids on the E2 DNA Binding Domain Define the Surface for Interaction with E1
- 1 February 2000
- journal article
- research article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 74 (3) , 1506-1512
- https://doi.org/10.1128/jvi.74.3.1506-1512.2000
Abstract
The E1 and E2 proteins from bovine papillomavirus bind cooperatively to the viral origin of DNA replication (ori), forming a complex which is essential for initiation of DNA replication. Cooperative binding has two components, in which (i) the DNA binding domains (DBDs) of the two proteins interact with each other and (ii) the E2 transactivation domain interacts with the helicase domain of E1. By generating specific point mutations in the DBD of E2, we have defined two patches of amino acids that are involved in the interaction with the E1 DBD. These same mutations, when introduced into the viral genome, result in severely reduced replication of the viral genome, as well as failure to transform mouse cells in tissue culture. Thus, the interaction between the E1 and E2 DBDs is important for the establishment of the viral genome as an episome and most likely contributes to the formation of a preinitiation complex on the viral ori.Keywords
This publication has 24 references indexed in Scilit:
- Architectural Transcription Factors: Proteins That-Remodel DNACell, 1997
- Homeodomain interactionsCurrent Opinion in Structural Biology, 1996
- Intercalation, DNA Kinking, and the Control of TranscriptionScience, 1996
- Crystal Structure of the MATa1/MATα2 Homeodomain Heterodimer Bound to DNAScience, 1995
- Homeodomain Proteins: Cooperating to be differentCurrent Biology, 1995
- Raster3D Version 2.0. A program for photorealistic molecular graphicsActa Crystallographica Section D-Biological Crystallography, 1994
- Crystal structure at 1.7 Å of the bovine papillomavirus-1 E2 DMA-binding domain bound to its DNA targetNature, 1992
- MOLSCRIPT: a program to produce both detailed and schematic plots of protein structuresJournal of Applied Crystallography, 1991
- Targeting the E1 Replication Protein to the Papillomavirus Origin of Replication by Complex Formation with the E2 TransactivatorScience, 1990
- Action at a Distance Along a DNAScience, 1988