A novel mechanism of E2F1 regulation via nucleocytoplasmic shuttling: determinants of nuclear import and export

Cell Cycle. 2007 Sep 1;6(17):2186-95. doi: 10.4161/cc.6.17.4650. Epub 2007 Jul 2.

Abstract

E2F1 is a transcription factor central for cell survival, proliferation, and repair following genomic insult. Depending on the cell type and conditions, E2F1 can induce apoptosis in transformed cells, behaving as a tumour suppressor, or impart growth advantages favouring tumour formation. The pleiotropic functions of E2F1 are a likely consequence of its ability to transcriptionally control a wide variety of target genes, and require tight regulation of its activity at multiple levels. Although sequestration of proteins to particular cellular compartments is a well-established regulatory mechanism, virtually nothing is known about its contribution to modulation of E2F1 target gene expression. We have examined the subcellular trafficking of E2F1 and, contrary to the widely held notion that this factor is constitutively nuclear, we now demonstrate that it is subjected to continuous nucleocytoplasmic shuttling. We have also defined two nuclear localization domains and a nuclear export region, which mediates CRM1-dependent transit out of the nucleus. The predominant subcellular location of E2F1 is likely determined by the balance between the activity of nuclear import and export domains, and can be modulated by differentiation stimuli in epidermal cells. Thus, we have identified a hitherto unrecognized mechanism to control E2F1 function through modulation of its subcellular localization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Apoptosis
  • Cell Differentiation
  • Cell Nucleus / metabolism*
  • Cell Transformation, Neoplastic
  • Cells, Cultured
  • E2F1 Transcription Factor / chemistry
  • E2F1 Transcription Factor / genetics
  • E2F1 Transcription Factor / metabolism*
  • Exportin 1 Protein
  • HeLa Cells
  • Humans
  • Karyopherins / metabolism
  • Keratinocytes / cytology
  • Keratinocytes / metabolism
  • Mice
  • Nuclear Localization Signals
  • Nucleocytoplasmic Transport Proteins / metabolism*
  • Protein Structure, Tertiary
  • Protein Transport
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Structure-Activity Relationship
  • Subcellular Fractions / metabolism
  • Transcription, Genetic

Substances

  • E2F1 Transcription Factor
  • Karyopherins
  • Nuclear Localization Signals
  • Nucleocytoplasmic Transport Proteins
  • Receptors, Cytoplasmic and Nuclear