Abstract
In breast cancer cells, cytoplasmic localization of the estradiol receptor alpha (ERalpha) regulates estradiol-dependent S phase entry. We identified a nuclear export sequence (NES) in ERalpha and show that its export is dependent on both estradiol-mediated phosphatidylinositol-3-kinase (PI3K)/AKT activation and chromosome region maintenance 1 (CRM1). A Tat peptide containing the ERalpha NES disrupts ERalpha-CRM1 interaction and prevents nuclear export of ERalpha- and estradiol-induced DNA synthesis. NES-ERalpha mutants do not exit the nucleus and inhibit estradiol-induced S phase entry; ERalpha-dependent transcription is normal. ERalpha is associated with Forkhead proteins in the nucleus, and estradiol stimulates nuclear exit of both proteins. ERalpha knockdown or ERalpha NES mutations prevent ERalpha and Forkhead nuclear export. A mutant of forkhead in rhabdomyosarcoma (FKHR), which cannot be phosphorylated by estradiol-activated AKT, does not associate with ERalpha and is trapped in the nucleus, blocking S phase entry. In conclusion, estradiol-induced AKT-dependent phosphorylation of FKHR drives its association with ERalpha, thereby triggering complex export from the nucleus necessary for initiation of DNA synthesis and S phase entry.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Active Transport, Cell Nucleus / drug effects
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Active Transport, Cell Nucleus / physiology
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Animals
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Breast Neoplasms / genetics
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Breast Neoplasms / metabolism*
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Carcinoma / genetics
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Carcinoma / metabolism*
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Cell Line, Tumor
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Cell Nucleus / metabolism*
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DNA, Neoplasm / biosynthesis*
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DNA, Neoplasm / genetics
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Estradiol / metabolism*
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Estradiol / pharmacology
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Estrogen Receptor alpha / drug effects
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Estrogen Receptor alpha / genetics
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Estrogen Receptor alpha / metabolism*
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Exportin 1 Protein
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Female
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Forkhead Box Protein O1
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Forkhead Transcription Factors / genetics
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Forkhead Transcription Factors / metabolism
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Genes, cdc / physiology
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Humans
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Karyopherins / genetics
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Karyopherins / metabolism
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Mice
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Mutation / genetics
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NIH 3T3 Cells
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Nuclear Export Signals / genetics
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Phosphatidylinositol 3-Kinases / genetics
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Phosphatidylinositol 3-Kinases / metabolism
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Proto-Oncogene Proteins c-akt / genetics
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Proto-Oncogene Proteins c-akt / metabolism
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Receptors, Cytoplasmic and Nuclear / genetics
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Receptors, Cytoplasmic and Nuclear / metabolism
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S Phase / genetics
Substances
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DNA, Neoplasm
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Estrogen Receptor alpha
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FOXO1 protein, human
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Forkhead Box Protein O1
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Forkhead Transcription Factors
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Karyopherins
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Nuclear Export Signals
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Receptors, Cytoplasmic and Nuclear
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Estradiol
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Phosphatidylinositol 3-Kinases
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Proto-Oncogene Proteins c-akt