Nm23/nucleoside diphosphate kinase: toward a structural and biochemical understanding of its biological functions

Bioessays. 1995 Jan;17(1):53-62. doi: 10.1002/bies.950170111.

Abstract

The nm23 gene, a putative metastasis suppressor gene, was originally identified by its reduced expression in highly metastatic K-1735 murine melanoma cell lines, as compared to related, low metastatic melanoma cell lines. Transfection of nm23 cDNA has been reported to suppress malignant progression in Drosophila and mammalian cells. Highly conserved homologues of nm23 have been found in organisms ranging from the prokaryote Myxococcus xanthus to Drosophila, where the gene is involved in normal development and differentiation. The product of the nm23 gene exhibits a nucleoside diphosphate kinase activity, yet the nucleoside diphosphate kinase activity of Nm23 does not correlate with its apparent biological functions. We review recent cellular, genetic, biochemical and X-ray crystallographic data to formulate and evaluate hypotheses concerning the molecular mechanism of nm23 action.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Drosophila
  • Genes, Tumor Suppressor
  • Guinea Pigs
  • Mice
  • Monomeric GTP-Binding Proteins*
  • NM23 Nucleoside Diphosphate Kinases
  • Nucleoside-Diphosphate Kinase* / chemistry
  • Nucleoside-Diphosphate Kinase* / genetics
  • Nucleoside-Diphosphate Kinase* / metabolism
  • Protein Conformation
  • Structure-Activity Relationship
  • Transcription Factors* / chemistry
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism

Substances

  • NM23 Nucleoside Diphosphate Kinases
  • Transcription Factors
  • Nme1 protein, mouse
  • Nucleoside-Diphosphate Kinase
  • Monomeric GTP-Binding Proteins