The NH2 terminus of galectin-3 governs cellular compartmentalization and functions in cancer cells

Cancer Res. 1999 Dec 15;59(24):6239-45.

Abstract

Galectin-3 is a member of the beta-galactoside-binding protein family shown to be involved in tumor progression and metastasis. It has a unique primary structure consisting of three domains: a 12-amino acid leader sequence containing a casein kinase I serine phosphorylation site, which is preceded by a collagenase-sensitive Pro-Gly-rich motif, and a COOH-terminal half encompassing the carbohydrate-binding site. To study the functional role of the unusual leader sequence of galectin-3, a mutant cDNA that causes an 11-amino acid deletion in the NH2-terminal region was generated and expressed in galectin-3-null BT-549 human breast carcinoma cells. Deletion of the NH2 terminus resulted in abolition of the secretion of truncated galectin-3, loss of nuclear localization, and reduced carbohydrate-mediated functions compared with the wild-type protein. When green fluorescent protein was fused to the galectin-3 leader sequence and transiently transfected into BT-549 cells, the uniform cellular distribution of native green fluorescent protein was changed mainly to a nuclear pattern. To further investigate whether the functional changes observed in a galectin-3 with the 11 NH2-terminal amino acids deleted were due to loss of phosphorylation at Ser6, two point mutations were created at this serine: Ser6-->Ala and Ser6-->Glu. No obvious difference was observed in cellular localization between wild-type and Ser6-mutated transfectants. These results suggest a structural role for the NH2 terminus leader motif of galectin-3 in determining its cellular targeting and biological functions independent of phosphorylation.

Publication types

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

MeSH terms

  • Antigens, Differentiation / biosynthesis
  • Antigens, Differentiation / genetics
  • Antigens, Differentiation / physiology*
  • Binding Sites
  • Biological Transport
  • Casein Kinases
  • Cell Compartmentation*
  • Cell Division / physiology
  • Cell Transformation, Neoplastic
  • DNA, Complementary
  • Galectin 3
  • Gene Deletion
  • Hemagglutination
  • Humans
  • Mutagenesis, Site-Directed
  • Neoplasms / metabolism
  • Peptide Fragments / physiology
  • Phosphorylation
  • Protein Kinases / metabolism
  • Serine / metabolism
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Antigens, Differentiation
  • DNA, Complementary
  • Galectin 3
  • Peptide Fragments
  • Serine
  • Protein Kinases
  • Casein Kinases