Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 97, Issue 16, Pages 8985-8990Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.160257997
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The thyroid hormone 3,3',5-triiodo-L-thyronine (T3) is essential for growth, differentiation, and development. Its biological activities are mediated by T3 nuclear receptors (TRs), At present, how T3 regulates TR proteins and the resulting functional consequences are still unknown. Immunofluorescence analyses of endogenous TR in the growth hormone-producing GC cells showed that the T3-induced rapid degradation of TR was specifically blocked by lactacystin, a selective inhibitor of the ubiquitin-proteasome degradation pathway. Immunoblots demonstrated that the transfected TR beta 1 was ubiquitinated and that the ubiquitination was T3 independent. Studies with a series of truncated TR beta 1 showed that the hormone-binding domain was sufficient for the T3-induced rapid degradation of TR beta 1 by the proteasome degradation pathway. T3 also induced rapid degradation of TR beta 2 and TR alpha 1. In contrast, the stability of the non-T3-binding TR alpha 2 and naturally occurring TR beta 1 mutants that do not bind T3 was not affected by T3 treatment, indicating that hormone binding to receptor was essential for the degradation of the wild type receptors. In the presence of proteasome protease inhibitors, the levels of both total and ubiquitinated TR beta 1 protein increased, yet T3-dependent transcriptional activation and the expression of the growth hormone gene were diminished, suggesting that proteasome-mediated degradation played a novel role in modulating transcriptional activation by TR. The present study reveals a role of T3 in modulating the functions of Tn by regulating its receptor level via the ubiquitin-proteasome degradation pathway.
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