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Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure

BACKGROUND: Non-coding RNAs have gained increasing attention during the last decade. The first large group of non-coding RNAs to be characterized systematically starting at the beginning of the 21st century were small oligonucleotides—the so-called microRNAs (miRNAs). By now we have learnt that micr...

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Autores principales: Bartram, Malte P., Amendola, Elena, Benzing, Thomas, Schermer, Bernhard, de Vita, Gabriella, Müller, Roman-Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835897/
https://www.ncbi.nlm.nih.gov/pubmed/27090781
http://dx.doi.org/10.1186/s12867-016-0064-x
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author Bartram, Malte P.
Amendola, Elena
Benzing, Thomas
Schermer, Bernhard
de Vita, Gabriella
Müller, Roman-Ulrich
author_facet Bartram, Malte P.
Amendola, Elena
Benzing, Thomas
Schermer, Bernhard
de Vita, Gabriella
Müller, Roman-Ulrich
author_sort Bartram, Malte P.
collection PubMed
description BACKGROUND: Non-coding RNAs have gained increasing attention during the last decade. The first large group of non-coding RNAs to be characterized systematically starting at the beginning of the 21st century were small oligonucleotides—the so-called microRNAs (miRNAs). By now we have learnt that microRNAs are indispensable for most biological processes including organogenesis and maintenance of organ structure and function. The role of microRNAs has been studied extensively in the development of a number of organs, so far most studies focussed on e.g. the heart or the brain whilst the role of microRNAs in the development and maintenance of complex epithelial organs is less well understood. Furthermore most analyses regarding microRNA function in epithelial organs employed conditional knockout mouse models of the RNAse III Dicer to abrogate microRNA biogenesis. However, there is increasing evidence for Dicer to have multiple functions independent from microRNA maturation. Therefore Dicer independent models are needed to gain further insight into the complex biology of miRNA dependent processes. RESULTS: Here we analyze the contribution of microRNA-dependent transcriptional control in Pax8-expressing epithelial cells. Pax8 is a transcription factor that is crucial to the development of epithelial organs. The miRNA machinery was disrupted by crossing conditional DiGeorge syndrome critical region 8(Dgcr8) fl/fl mice to Pax8Cre mice. The Dgcr8/Drosha complex processes pri-miRNAs in the nucleus before they are exported as pre-miRNAs for further maturation by Dicer in the cytoplasm. Dgcr8 fl/fl; Pax8Cre+ knockout mice died prematurely, developed massive hypothyroidism and end stage renal disease due to a loss of miRNAs in Pax8 expressing tissue. CONCLUSION: Pax8Cre-mediated conditional loss of DiGeorge syndrome critical region 8 (Dgcr8), an essential component of the nuclear machinery that is required for microRNA biogenesis, resulted in severe hypothyroidism, massively reduced body weight and ultimately led to renal failure and death of the animals. These data provide further insight into the importance of miRNAs in organ homeostasis using a Dicer independent model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12867-016-0064-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-48358972016-04-20 Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure Bartram, Malte P. Amendola, Elena Benzing, Thomas Schermer, Bernhard de Vita, Gabriella Müller, Roman-Ulrich BMC Mol Biol Research Article BACKGROUND: Non-coding RNAs have gained increasing attention during the last decade. The first large group of non-coding RNAs to be characterized systematically starting at the beginning of the 21st century were small oligonucleotides—the so-called microRNAs (miRNAs). By now we have learnt that microRNAs are indispensable for most biological processes including organogenesis and maintenance of organ structure and function. The role of microRNAs has been studied extensively in the development of a number of organs, so far most studies focussed on e.g. the heart or the brain whilst the role of microRNAs in the development and maintenance of complex epithelial organs is less well understood. Furthermore most analyses regarding microRNA function in epithelial organs employed conditional knockout mouse models of the RNAse III Dicer to abrogate microRNA biogenesis. However, there is increasing evidence for Dicer to have multiple functions independent from microRNA maturation. Therefore Dicer independent models are needed to gain further insight into the complex biology of miRNA dependent processes. RESULTS: Here we analyze the contribution of microRNA-dependent transcriptional control in Pax8-expressing epithelial cells. Pax8 is a transcription factor that is crucial to the development of epithelial organs. The miRNA machinery was disrupted by crossing conditional DiGeorge syndrome critical region 8(Dgcr8) fl/fl mice to Pax8Cre mice. The Dgcr8/Drosha complex processes pri-miRNAs in the nucleus before they are exported as pre-miRNAs for further maturation by Dicer in the cytoplasm. Dgcr8 fl/fl; Pax8Cre+ knockout mice died prematurely, developed massive hypothyroidism and end stage renal disease due to a loss of miRNAs in Pax8 expressing tissue. CONCLUSION: Pax8Cre-mediated conditional loss of DiGeorge syndrome critical region 8 (Dgcr8), an essential component of the nuclear machinery that is required for microRNA biogenesis, resulted in severe hypothyroidism, massively reduced body weight and ultimately led to renal failure and death of the animals. These data provide further insight into the importance of miRNAs in organ homeostasis using a Dicer independent model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12867-016-0064-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-18 /pmc/articles/PMC4835897/ /pubmed/27090781 http://dx.doi.org/10.1186/s12867-016-0064-x Text en © Bartram et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bartram, Malte P.
Amendola, Elena
Benzing, Thomas
Schermer, Bernhard
de Vita, Gabriella
Müller, Roman-Ulrich
Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
title Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
title_full Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
title_fullStr Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
title_full_unstemmed Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
title_short Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
title_sort mice lacking micrornas in pax8-expressing cells develop hypothyroidism and end-stage renal failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835897/
https://www.ncbi.nlm.nih.gov/pubmed/27090781
http://dx.doi.org/10.1186/s12867-016-0064-x
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