Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34924
Title: Fundamentally Distinct Roles of Thyroid Hormone Receptor Isoforms in a Thyrotroph Cell Line Are due to Differential DNA Binding
Authors: Chiamolera, Maria Izabel [UNIFESP]
Sidhaye, Aniket R.
Matsumoto, Shunichi
He, Qiyi
Hashimoto, Koshi
Ortiga-Carvalho, Tania M.
Wondisford, Fredric E.
Johns Hopkins Univ
Universidade Federal de São Paulo (UNIFESP)
Gunma Univ
Universidade Federal do Rio de Janeiro (UFRJ)
Issue Date: 1-Jun-2012
Publisher: Endocrine Soc
Citation: Molecular Endocrinology. Chevy Chase: Endocrine Soc, v. 26, n. 6, p. 926-939, 2012.
Abstract: Thyroid hormones have a profound influence on human development and disease. the hypothalamic- pituitary-thyroid axis involves finely tuned feedback mechanisms to maintain thyroid hormone (TH) levels. Despite the important role of TH-negative feedback in regulating this axis, the mechanism by which this occurs is not clearly defined. Previous in vivo studies suggest separate roles for the two thyroid hormone receptor isoforms, THRA and THRB, in this axis. We performed studies using a unique pituitary thyrotroph cell line (T alpha T1.1) to determine the relative roles of THRA and THRB in the regulation of Tshb. Using chromatin immunoprecipitation assays, we found that THRB, not THRA, bound to the Tshb promoter. By selectively depleting THRB, THRA, or both THRA and THRB in T alpha T1.1 cells, we found that simultaneous knockdown of both THRB and THRA abolished T-3-mediated down-regulation of Tshb at concentrations as high as 100 nM T-3. in contrast, THRA knockdown alone had no effect on T-3-negative regulation, whereas THRB knockdown alone abolished T-3-mediated down-regulation of Tshb mRNA levels at 10 nM but not 100 nM T-3 concentrations. Interestingly, chromatin immunoprecipitation assays showed that THRA becomes enriched on the Tshb promoter after knockdown of THRB. Thus, a likely mechanism for the differential effects of THR isoforms on Tshb may be based on their differential DNA-binding affinity to the promoter. (Molecular Endocrinology 26: 926-939, 2012)
URI: http://repositorio.unifesp.br/handle/11600/34924
ISSN: 0888-8809
Other Identifiers: http://dx.doi.org/10.1210/me.2011-1290
Appears in Collections:Em verificação - Geral

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