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To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?

The terrain is well explored regarding genes whose gene expression is up-regulated upon binding of thyroid hormone (TH) to its nuclear receptor. This regulation mechanism has been intensively studied and is well understood. In contrast, a lot of white spots remain on the map when it comes to target...

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Autor principal: Weitzel, Joachim M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2583983/
https://www.ncbi.nlm.nih.gov/pubmed/19014660
http://dx.doi.org/10.1186/1756-6614-1-4
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author Weitzel, Joachim M
author_facet Weitzel, Joachim M
author_sort Weitzel, Joachim M
collection PubMed
description The terrain is well explored regarding genes whose gene expression is up-regulated upon binding of thyroid hormone (TH) to its nuclear receptor. This regulation mechanism has been intensively studied and is well understood. In contrast, a lot of white spots remain on the map when it comes to target genes whose expression is down-regulated upon binding of TH to the thyroid hormone receptor (TR). Since no consistent mechanism has been proposed to explain ligand-dependent down-regulation of target gene transcription several working hypotheses favour different molecular mechanisms. Some working theories suggest a direct binding of TR to regulatory elements of target genes. Others favour models that are independent of a direct DNA binding event. However recent data suggested that a direct binding of TR to DNA is dispensable for TH-dependent negative gene transcription.
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spelling pubmed-25839832008-11-18 To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor? Weitzel, Joachim M Thyroid Res Commentary The terrain is well explored regarding genes whose gene expression is up-regulated upon binding of thyroid hormone (TH) to its nuclear receptor. This regulation mechanism has been intensively studied and is well understood. In contrast, a lot of white spots remain on the map when it comes to target genes whose expression is down-regulated upon binding of TH to the thyroid hormone receptor (TR). Since no consistent mechanism has been proposed to explain ligand-dependent down-regulation of target gene transcription several working hypotheses favour different molecular mechanisms. Some working theories suggest a direct binding of TR to regulatory elements of target genes. Others favour models that are independent of a direct DNA binding event. However recent data suggested that a direct binding of TR to DNA is dispensable for TH-dependent negative gene transcription. BioMed Central 2008-10-11 /pmc/articles/PMC2583983/ /pubmed/19014660 http://dx.doi.org/10.1186/1756-6614-1-4 Text en Copyright © 2008 Weitzel; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Weitzel, Joachim M
To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
title To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
title_full To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
title_fullStr To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
title_full_unstemmed To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
title_short To bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
title_sort to bind or not to bind – how to down-regulate target genes by liganded thyroid hormone receptor?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2583983/
https://www.ncbi.nlm.nih.gov/pubmed/19014660
http://dx.doi.org/10.1186/1756-6614-1-4
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