Colocalization and identification of interaction sites between IGFBP-3 and GalNAc-T14

Gene. 2012 May 15;499(2):347-51. doi: 10.1016/j.gene.2012.03.015. Epub 2012 Mar 14.

Abstract

GalNAc-T14 was identified as a novel IGFBP-3 binding partner in previous studies. Here, we furtherly confirmed the interaction between them by confocal microscopy, and identified the binding domain and probable interaction sites of GalNAc-T14 with IGFBP-3. The result of subcellular localization indicated that GalNAc-T14 was distributed in the cytosol, whereas IGFBP-3 existed in the cytosol and nucleolus. Confocal analyses demonstrated that IGFBP-3 and GalNAc-T14 colocalized in the cytosol. The result from yeast two hybrid assay showed that the C terminus of GalNAc-T14 (408-552aa) was essential for the interaction between GalNAc-T14 and IGFBP-3, especially Tyr(408), Pro(409), and Glu(410) of GalNAc-T14 may play key roles in the interaction with IGFBP-3. In conclusion, these studies demonstrated that IGFBP-3 and GalNAc-T14 are colocalized in MCF-7 cells and confirmed the interaction between IGFBP-3 and GalNAc-T14. This interaction may play an important role in the functional regulation of IGFBP-3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Humans
  • Insulin-Like Growth Factor Binding Protein 3 / analysis
  • Insulin-Like Growth Factor Binding Protein 3 / chemistry*
  • Insulin-Like Growth Factor Binding Protein 3 / metabolism*
  • Microscopy, Confocal
  • Models, Molecular
  • N-Acetylgalactosaminyltransferases / analysis
  • N-Acetylgalactosaminyltransferases / chemistry*
  • N-Acetylgalactosaminyltransferases / metabolism*
  • Protein Interaction Domains and Motifs
  • Two-Hybrid System Techniques

Substances

  • IGFBP3 protein, human
  • Insulin-Like Growth Factor Binding Protein 3
  • N-Acetylgalactosaminyltransferases
  • UDP-N-acetyl-D-galactosamine polypeptide N-acetylgalactosaminyltransferase 14, human