Immediate early gene X1 (IEX-1) is organized in subnuclear structures and partially co-localizes with promyelocytic leukemia protein in HeLa cells

J Biol Chem. 2005 Jul 1;280(26):24849-56. doi: 10.1074/jbc.M501571200. Epub 2005 Apr 26.

Abstract

Immediate early gene X1 (IEX-1) represents a stress response gene involved in growth control and modulation of apoptosis. Here, we report a detailed analysis of IEX-1 with respect to its intracellular localization. By means of confocal laser scanning microscopy, a green fluorescent protein-IEX-1 fusion protein transfected into HeLa cells, as well as endogenous IEX-1, could be detected in distinct subnuclear structures. This particular subnuclear localization of IEX-1 was not observed with a green fluorescent protein-IEX-1 fusion protein lacking a putative nuclear localization sequence, along with a decreased effect on apoptosis. Double immunofluorescence staining revealed a partial co-localization of endogenous promyelocytic leukemia protein (PML) and IEX-1 in these subnuclear structures. Nuclear localization of IEX-1 is also enhanced upon treatment of cells with leptomycin B, an inhibitor of the nuclear exporter CRM1. These observations indicate that IEX-1 is specifically shuttled to and from the nucleus. Overexpression experiments using PML isoforms III and IV revealed distinct intranuclear interaction of IEX-1 and PML. Coprecipitation experiments showed physical interaction between IEX-1 and PML. The close structural relation of IEX-1-containing nuclear subdomains and PML nuclear bodies suggests a function of IEX-1 related to the multiple functions of these unique subnuclear regions, particularly during stress response and growth control.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Apoptosis
  • Apoptosis Regulatory Proteins
  • Blotting, Western
  • Caspases / metabolism
  • Cell Nucleus / metabolism*
  • Fatty Acids, Unsaturated / pharmacology
  • Genes, Immediate-Early*
  • Glutathione Transferase / metabolism
  • Green Fluorescent Proteins / chemistry
  • Green Fluorescent Proteins / metabolism
  • HeLa Cells
  • Humans
  • Immediate-Early Proteins / genetics*
  • Immediate-Early Proteins / physiology*
  • Immunoprecipitation
  • Membrane Proteins
  • Microscopy, Confocal
  • Microscopy, Fluorescence
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Neoplasm Proteins / physiology*
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / physiology*
  • Promyelocytic Leukemia Protein
  • Protein Binding
  • Protein Isoforms
  • Recombinant Fusion Proteins / chemistry
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • Transfection
  • Tumor Suppressor Proteins / metabolism
  • Tumor Suppressor Proteins / physiology*

Substances

  • Apoptosis Regulatory Proteins
  • Fatty Acids, Unsaturated
  • IER3 protein, human
  • Immediate-Early Proteins
  • Membrane Proteins
  • Neoplasm Proteins
  • Nuclear Proteins
  • Promyelocytic Leukemia Protein
  • Protein Isoforms
  • Recombinant Fusion Proteins
  • Transcription Factors
  • Tumor Suppressor Proteins
  • PML protein, human
  • Green Fluorescent Proteins
  • Glutathione Transferase
  • Caspases
  • leptomycin B