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Author Spotlight: In Vivo Assessment of Thyroid Hormone Disruption Using the THAI Mouse Model
Published on: October 6, 2023
Thyroid hormone receptor localization in target tissues
Cyril S Anyetei-Anum1, Vincent R Roggero1, Lizabeth A Allison2
1Department of BiologyCollege of William and Mary, Williamsburg, Virginia, USA.
Abstract:
The thyroid hormone receptors, TRα1, TRβ1 and other subtypes, are members of the nuclear receptor superfamily that mediate the action of thyroid hormone signaling in numerous tissues to regulate important physiological and developmental processes. Their most well-characterized role is as ligand-dependent transcription factors; TRs bind thyroid hormone response elements in the presence or absence of thyroid hormone to facilitate the expression of target genes. Although primarily residing in the nucleus, TRα1 and TRβ1 shuttle rapidly between the nucleus and cytoplasm. We have identified multiple nuclear localization signals and nuclear export signals within TRα1 and TRβ1 that interact with importins and exportins, respectively, to mediate translocation across the nuclear envelope. More recently, enigmatic cytoplasmic functions have been ascribed to other TR subtypes, expanding the diversity of the cellular response to thyroid hormone. By integrating data on localization signal motifs, this review provides an overview of the complex interplay between TR's dynamic transport pathways and thyroid hormone signaling activities. We examine the variation in TR subtype response to thyroid hormone signaling, and what is currently known about regulation of the variety of tissue-specific localization patterns, including targeting to the nucleus, the mitochondria and the inner surface of the plasma membrane.
Insights
Thyroid hormone receptors (TRs) regulate gene expression and physiological processes. This review details TR subtype transport between the nucleus and cytoplasm, influencing thyroid hormone signaling.
Area of Science:
- Molecular Endocrinology
- Nuclear Receptor Signaling
Background:
- Thyroid hormone receptors (TRs) are nuclear receptors crucial for physiological and developmental processes.
- TRs function as ligand-dependent transcription factors, regulating target gene expression.
Purpose of the Study:
- To review the dynamic transport pathways of TR subtypes between the nucleus and cytoplasm.
- To explore the interplay between TR localization and thyroid hormone signaling.
- To examine tissue-specific localization patterns and emerging cytoplasmic functions of TRs.
Main Methods:
- Integration of data on nuclear localization signals (NLS) and nuclear export signals (NES) within TR subtypes.
- Analysis of interactions with importins and exportins for nuclear translocation.
- Review of existing literature on TR localization and function.
Main Results:
- Identification of multiple NLS and NES in TRα1 and TRβ1, mediating nuclear import and export.
- Evidence for rapid nucleocytoplasmic shuttling of TRα1 and TRβ1.
- Emerging understanding of diverse cytoplasmic functions for other TR subtypes.
Conclusions:
- TR subtype localization is dynamic and regulated, involving complex transport pathways.
- Nucleocytoplasmic transport significantly influences thyroid hormone signaling activities.
- TRs exhibit tissue-specific localization, including to mitochondria and the plasma membrane, expanding their functional roles.
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