Identification of a nucleolin binding site in human topoisomerase I

J Biol Chem. 1996 Jan 26;271(4):1993-7. doi: 10.1074/jbc.271.4.1993.

Abstract

DNA topoisomerase I (topo I) is involved in the regulation of DNA supercoiling, gene transcription, and rDNA recombination. However, little is known about interactions between topo I and other nuclear proteins. We used affinity chromatography with a topo I fusion protein to screen U-937 leukemic cell extracts and have identified nucleolin as a topo I-binding protein. Coimmunoprecipitation and other studies demonstrate that the interaction between topo I and nucleolin is direct. Furthermore, deletion analyses have identified the 166-210-amino acid region of topo I as sufficient for the interaction with nucleolin. Since nucleolin has been implicated in nuclear transport and in a variety of transcriptional processes, the interaction with topo I may relate to the cellular localization of topo I or to the known role of this topoisomerase in transcription.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Cell Compartmentation
  • DNA Topoisomerases, Type I / chemistry*
  • DNA Topoisomerases, Type I / metabolism
  • DNA, Superhelical / metabolism
  • Humans
  • Molecular Sequence Data
  • Nuclear Proteins / chemistry*
  • Nuclear Proteins / metabolism
  • Nucleolin
  • Phosphoproteins / chemistry*
  • Phosphoproteins / metabolism
  • RNA-Binding Proteins*
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Tumor Cells, Cultured

Substances

  • DNA, Superhelical
  • Nuclear Proteins
  • Phosphoproteins
  • RNA-Binding Proteins
  • DNA Topoisomerases, Type I