Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8477010 | Molecular and Cellular Endocrinology | 2015 | 11 Pages |
Abstract
The thyroid hormone receptor (TR) undergoes nucleocytoplasmic shuttling and regulates target genes involved in metabolism and development. Previously, we showed that TR follows a CRM1/calreticulin-mediated nuclear export pathway. However, two lines of evidence suggest TR also follows another pathway: export is only partially blocked by leptomycin B (LMB), a CRM1-specific inhibitor; and we identified nuclear export signals in TR that are LMB-resistant. To determine whether other exportins are involved in TR shuttling, we used RNA interference and fluorescence recovery after photobleaching shuttling assays in transfected cells. Knockdown of exportins 4, 5, and 7 altered TR shuttling dynamics, and when exportins 5 and 7 were overexpressed, TR distribution shifted toward the cytosol. To further assess the effects of exportin overexpression, we examined transactivation of a TR-responsive reporter gene. Our data indicate that multiple exportins influence TR localization, highlighting a fine balance of nuclear import, retention, and export that modulates TR function.
Keywords
nESqPCRLMBGFPCrm1WGAshRNAFRAPNLSQuantitative PCRRNA interferenceRNAishort hairpin RNATREnuclear export signalnuclear localization signalExportinNuclear exportThyroid hormone response elementfluorescence recovery after photobleachingLeptomycin BMicroRNAMiRNAchromosome region maintenance 1Thyroid hormonegreen fluorescent proteinWheat germ agglutininthyroid hormone receptor
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Authors
Kelly S. Subramanian, Rose C. Dziedzic, Hallie N. Nelson, Mary E. Stern, Vincent R. Roggero, Cornelius Bondzi, Lizabeth A. Allison,