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The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes

Abnormalities are indispensable for studying normal biological processes and mechanisms. In the present work, we draw attention to the remarkable phenomenon of a perpetually and robustly upregulated gene, the thyroglobulin gene (Tg). The gene is expressed in the thyroid gland and, as it has been rec...

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Autores principales: Ullrich, Simon, Leidescher, Susanne, Feodorova, Yana, Thanisch, Katharina, Fini, Jean-Baptiste, Kaspers, Bernd, Weber, Frank, Markova, Boyka, Führer, Dagmar, Romitti, Mirian, Krebs, Stefan, Blum, Helmut, Leonhardt, Heinrich, Costagliola, Sabine, Heuer, Heike, Solovei, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582334/
https://www.ncbi.nlm.nih.gov/pubmed/37860816
http://dx.doi.org/10.3389/fcell.2023.1265407
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author Ullrich, Simon
Leidescher, Susanne
Feodorova, Yana
Thanisch, Katharina
Fini, Jean-Baptiste
Kaspers, Bernd
Weber, Frank
Markova, Boyka
Führer, Dagmar
Romitti, Mirian
Krebs, Stefan
Blum, Helmut
Leonhardt, Heinrich
Costagliola, Sabine
Heuer, Heike
Solovei, Irina
author_facet Ullrich, Simon
Leidescher, Susanne
Feodorova, Yana
Thanisch, Katharina
Fini, Jean-Baptiste
Kaspers, Bernd
Weber, Frank
Markova, Boyka
Führer, Dagmar
Romitti, Mirian
Krebs, Stefan
Blum, Helmut
Leonhardt, Heinrich
Costagliola, Sabine
Heuer, Heike
Solovei, Irina
author_sort Ullrich, Simon
collection PubMed
description Abnormalities are indispensable for studying normal biological processes and mechanisms. In the present work, we draw attention to the remarkable phenomenon of a perpetually and robustly upregulated gene, the thyroglobulin gene (Tg). The gene is expressed in the thyroid gland and, as it has been recently demonstrated, forms so-called transcription loops, easily observable by light microscopy. Using this feature, we show that Tg is expressed at a high level from the moment a thyroid cell acquires its identity and both alleles remain highly active over the entire life of the cell, i.e., for months or years depending on the species. We demonstrate that this high upregulation is characteristic of thyroglobulin genes in all major vertebrate groups. We provide evidence that Tg is not influenced by the thyroid hormone status, does not oscillate round the clock and is expressed during both the exocrine and endocrine phases of thyrocyte activity. We conclude that the thyroglobulin gene represents a unique and valuable model to study the maintenance of a high transcriptional upregulation.
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spelling pubmed-105823342023-10-19 The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes Ullrich, Simon Leidescher, Susanne Feodorova, Yana Thanisch, Katharina Fini, Jean-Baptiste Kaspers, Bernd Weber, Frank Markova, Boyka Führer, Dagmar Romitti, Mirian Krebs, Stefan Blum, Helmut Leonhardt, Heinrich Costagliola, Sabine Heuer, Heike Solovei, Irina Front Cell Dev Biol Cell and Developmental Biology Abnormalities are indispensable for studying normal biological processes and mechanisms. In the present work, we draw attention to the remarkable phenomenon of a perpetually and robustly upregulated gene, the thyroglobulin gene (Tg). The gene is expressed in the thyroid gland and, as it has been recently demonstrated, forms so-called transcription loops, easily observable by light microscopy. Using this feature, we show that Tg is expressed at a high level from the moment a thyroid cell acquires its identity and both alleles remain highly active over the entire life of the cell, i.e., for months or years depending on the species. We demonstrate that this high upregulation is characteristic of thyroglobulin genes in all major vertebrate groups. We provide evidence that Tg is not influenced by the thyroid hormone status, does not oscillate round the clock and is expressed during both the exocrine and endocrine phases of thyrocyte activity. We conclude that the thyroglobulin gene represents a unique and valuable model to study the maintenance of a high transcriptional upregulation. Frontiers Media S.A. 2023-10-04 /pmc/articles/PMC10582334/ /pubmed/37860816 http://dx.doi.org/10.3389/fcell.2023.1265407 Text en Copyright © 2023 Ullrich, Leidescher, Feodorova, Thanisch, Fini, Kaspers, Weber, Markova, Führer, Romitti, Krebs, Blum, Leonhardt, Costagliola, Heuer and Solovei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Ullrich, Simon
Leidescher, Susanne
Feodorova, Yana
Thanisch, Katharina
Fini, Jean-Baptiste
Kaspers, Bernd
Weber, Frank
Markova, Boyka
Führer, Dagmar
Romitti, Mirian
Krebs, Stefan
Blum, Helmut
Leonhardt, Heinrich
Costagliola, Sabine
Heuer, Heike
Solovei, Irina
The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
title The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
title_full The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
title_fullStr The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
title_full_unstemmed The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
title_short The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
title_sort highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582334/
https://www.ncbi.nlm.nih.gov/pubmed/37860816
http://dx.doi.org/10.3389/fcell.2023.1265407
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