Id3 modulates cellular localization of bHLH Ptf1-p48 protein

Int J Cancer. 2011 Jul 15;129(2):295-306. doi: 10.1002/ijc.25668. Epub 2010 Nov 3.

Abstract

Ptf1-p48 is a pancreas-specific bHLH transcriptional protein, which, in the normal adult pancreas, shows a restricted expression in acinar cells where it is predominantly localized in the nucleus and activates the transcription of exocrine-specific genes. Ptf1-p48 partners with two proteins to form the PTF1 active complex: a bHLH E-protein and suppressor of hairless RBP-J. Cytoplasmic mislocalization of Ptf1-p48 has been reported in pancreatic pathologies, suggesting its contribution in the early steps of pancreatic carcinogenesis. The aim of the our work was to elucidate the mechanisms regulating Ptf1-p48 subcellular localization. We hypothesized a role of Id proteins acting in a dominant-negative fashion by heterodimerizing with bHLH proteins. We reproduced Ptf1-p48 cytoplasmic mislocalization in acinar AR4-2J cells and demonstrated that a proliferative signal elicited by gastrin leads to increases in Id3 protein expression and levels of Id3/E47 and Id3/Ptf1-p48 interactions, and a decrease in the level of E47/Ptf1-p48 interaction. By contrast, Id3 silencing reversed the cytoplasmic mislocalization of Ptf1-p48 induced by gastrin. As E47 is responsible for the nuclear import of the PTF1 complex, disruption of this complex via Id3 interactions with both E47 and Ptf1-p48 appears to induce cytoplasmic mislocalization of Ptf1-p48. We then found that Ptf1-p48 is either absent or mislocalized in the cytoplasm and Id3 is overexpressed in human and murine pancreatic preneoplastic lesions. Our data provide novel insight into the regulation of Ptf1-p48 function and provide evidence that Ptf1-p48 cytoplasmic mislocalization and Id3 overexpression are early events in pancreatic cancer progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / metabolism
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Cytoplasm / metabolism
  • Disease Models, Animal
  • Humans
  • Inhibitor of Differentiation Proteins / metabolism
  • Inhibitor of Differentiation Proteins / physiology*
  • Interferon-Stimulated Gene Factor 3, gamma Subunit / metabolism
  • Mice
  • Mice, Transgenic
  • Neoplasm Proteins / metabolism
  • Neoplasm Proteins / physiology*
  • Pancreatic Neoplasms / metabolism
  • Protein Transport
  • Rabbits
  • Rats
  • Transcription Factors / metabolism*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Inhibitor of Differentiation Proteins
  • Interferon-Stimulated Gene Factor 3, gamma Subunit
  • Isgf3g protein, mouse
  • Neoplasm Proteins
  • Transcription Factors
  • transcription factor PTF1
  • Idb3 protein, mouse
  • ID3 protein, human