Topological linkage of circular DNA molecules promoted by Ustilago rec 1 protein and topoisomerase

Cell. 1983 Oct;34(3):919-29. doi: 10.1016/0092-8674(83)90549-4.

Abstract

We studied the formation of linked circular DNA molecules promoted by the combined action of rec 1 protein and type I topoisomerase of Ustilago maydis. When ATP was added as cofactor to reactions containing rec 1 protein, pairs of homologous circular DNA molecules became linked after addition of topoisomerase. Closed circular duplex molecules could be joined at homologous sites with circular single-stranded molecules or with other circular duplex molecules, provided that homologous single-stranded DNA fragments or RNA polymerase and nucleoside triphosphates were also added. Complexes formed were topologically linked through regions of heteroduplex DNA. When the analog adenylyl-imidodiphosphate was substituted for ATP, nonhomologous pairs of circular DNA molecules became linked.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Adenylyl Imidodiphosphate / pharmacology
  • Basidiomycota / genetics*
  • DNA Topoisomerases, Type I / metabolism*
  • DNA, Circular / metabolism*
  • Exodeoxyribonuclease V
  • Fungal Proteins / pharmacology*
  • Genetic Linkage
  • Nucleic Acid Conformation / drug effects
  • Ustilago / genetics*

Substances

  • DNA, Circular
  • Fungal Proteins
  • Adenylyl Imidodiphosphate
  • Adenosine Triphosphate
  • Exodeoxyribonuclease V
  • DNA Topoisomerases, Type I