Transcription activator structure reveals redox control of a replication initiation reaction

Nucleic Acids Res. 2007;35(10):3504-15. doi: 10.1093/nar/gkm166. Epub 2007 May 3.

Abstract

Redox changes are one of the factors that influence cell-cycle progression and that control the processes of cellular proliferation, differentiation, senescence and apoptosis. Proteins regulated through redox-sensitive cysteines have been characterized but specific 'sulphydryl switches' in replication proteins remain to be identified. In bovine papillomavirus type-1, DNA replication begins when the viral transcription factor E2 recruits the viral initiator protein E1 to the origin of DNA replication (ori). Here we show that a novel dimerization interface in the E2 transcription activation domain is stabilized by a disulphide bond. Oxidative cross-linking via Cys57 sequesters the interaction surface between E1 and E2, preventing pre-initiation and replication initiation complex formation. Our data demonstrate that as well as a mechanism for regulating DNA binding, redox reactions can control replication by modulating the tertiary structure of critical protein factors using a specific redox sensor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray
  • Cysteine / chemistry
  • DNA / metabolism
  • DNA Replication*
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / metabolism
  • Dimerization
  • Models, Molecular
  • Oxidation-Reduction
  • Protein Structure, Tertiary
  • Replication Origin
  • Trans-Activators / chemistry*
  • Trans-Activators / metabolism
  • Viral Proteins / chemistry*
  • Viral Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • E1 protein, Bovine papillomavirus
  • E2 protein, Bovine papillomavirus
  • Trans-Activators
  • Viral Proteins
  • DNA
  • Cysteine

Associated data

  • PDB/2JEU
  • PDB/2JEX