کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2195630 1550854 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
3,5-Diiodothyronine-mediated transrepression of the thyroid hormone receptor beta gene in tilapia. Insights on cross-talk between the thyroid hormone and cortisol signaling pathways
ترجمه فارسی عنوان
ترانس سرکوب شده توسط 3،5-دیویدوترینرون به گیرنده هورمون تیروئید بتا در تیلاپیا. بینش در مورد متقابل بین هورمون تیروئید و مسیرهای سیگنالینگ کورتیزول
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
چکیده انگلیسی


• The proximal promoter (−1.5 Kb) of tilapia thrb contains putative TRE- and GRE-like half-sites.
• The proximal promoter (−1.5 Kb) of tilapia thrb presents transactivating activity and responds to T3, 3,5-T2 in GH3 cells.
• Nuclear proteins and putative tilapia thrb TRE- and GRE half-site complexes are destabilized by 3,5-T2 and stabilized by cortisol.
• 3,5-T2 transrepresses tilapia thrb expression and impairs its up-regulation by cortisol.

T3 and cortisol activate or repress gene expression in virtually every vertebrate cell mainly by interacting with their nuclear hormone receptors. In contrast to the mechanisms for hormone gene activation, the mechanisms involved in gene repression remain elusive. In teleosts, the thyroid hormone receptor beta gene or thrb produces two isoforms of TRβ1 that differ by nine amino acids in the ligand-binding domain of the long-TRβ1, whereas the short-TRβ1 lacks the insert. Previous reports have shown that the genomic effects exerted by 3,5-T2, a product of T3 outer-ring deiodination, are mediated by the long-TRβ1. Furthermore, 3,5-T2 and T3 down-regulate the expression of long-TRβ1 and short-TRβ1, respectively. In contrast, cortisol has been shown to up-regulate the expression of thrb. To understand the molecular mechanisms for thrb modulation by thyroid hormones and cortisol, we used an in silico approach to identify thyroid- and cortisol-response elements within the proximal promoter of thrb from tilapia. We then characterized the identified response elements by EMSA and correlated our observations with the effects of THs and cortisol upon expression of thrb in tilapia. Our data show that 3,5-T2 represses thrb expression and impairs its up-regulation by cortisol possibly through a transrepression mechanism. We propose that for thrb down-regulation, ligands other than T3 are required to orchestrate the pleiotropic effects of thyroid hormones in vertebrates.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular and Cellular Endocrinology - Volume 425, 15 April 2016, Pages 103–110
نویسندگان
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