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Differential regulation of transposable elements (TEs) during the murine submandibular gland development

The submandibular gland (SG) is a relatively simple organ formed by three cell types: acinar, myoepithelial, and an intricate network of duct-forming epithelial cells, that together fulfills several physiological functions from assisting food digestion to acting as an immune barrier against pathogen...

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Autores principales: Valdebenito-Maturana, Braulio, Torres, Francisca, Carrasco, Mónica, Tapia, Juan Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540199/
https://www.ncbi.nlm.nih.gov/pubmed/34686213
http://dx.doi.org/10.1186/s13100-021-00251-1
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author Valdebenito-Maturana, Braulio
Torres, Francisca
Carrasco, Mónica
Tapia, Juan Carlos
author_facet Valdebenito-Maturana, Braulio
Torres, Francisca
Carrasco, Mónica
Tapia, Juan Carlos
author_sort Valdebenito-Maturana, Braulio
collection PubMed
description The submandibular gland (SG) is a relatively simple organ formed by three cell types: acinar, myoepithelial, and an intricate network of duct-forming epithelial cells, that together fulfills several physiological functions from assisting food digestion to acting as an immune barrier against pathogens. Successful SG organogenesis is the product of highly controlled and orchestrated genetic and transcriptional programs. Mounting evidence links Transposable Elements (TEs), originally thought to be selfish genetic elements, to different aspects of gene regulation in mammalian development and disease. To our knowledge, the role of TEs during murine SG organogenesis has not been studied. Using novel bioinformatic tools and publicly available RNA-Seq datasets, our results indicate that a significant number of genic and intergenic TEs are differentially expressed during the SG development. Furthermore, changes in expression of specific TEs correlated with that of genes involved in cellular division and differentiation, critical aspects for SG maturation. Altogether, we propose that TEs modulate gene networks that operate during SG development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13100-021-00251-1.
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spelling pubmed-85401992021-10-25 Differential regulation of transposable elements (TEs) during the murine submandibular gland development Valdebenito-Maturana, Braulio Torres, Francisca Carrasco, Mónica Tapia, Juan Carlos Mob DNA Short Report The submandibular gland (SG) is a relatively simple organ formed by three cell types: acinar, myoepithelial, and an intricate network of duct-forming epithelial cells, that together fulfills several physiological functions from assisting food digestion to acting as an immune barrier against pathogens. Successful SG organogenesis is the product of highly controlled and orchestrated genetic and transcriptional programs. Mounting evidence links Transposable Elements (TEs), originally thought to be selfish genetic elements, to different aspects of gene regulation in mammalian development and disease. To our knowledge, the role of TEs during murine SG organogenesis has not been studied. Using novel bioinformatic tools and publicly available RNA-Seq datasets, our results indicate that a significant number of genic and intergenic TEs are differentially expressed during the SG development. Furthermore, changes in expression of specific TEs correlated with that of genes involved in cellular division and differentiation, critical aspects for SG maturation. Altogether, we propose that TEs modulate gene networks that operate during SG development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13100-021-00251-1. BioMed Central 2021-10-22 /pmc/articles/PMC8540199/ /pubmed/34686213 http://dx.doi.org/10.1186/s13100-021-00251-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Report
Valdebenito-Maturana, Braulio
Torres, Francisca
Carrasco, Mónica
Tapia, Juan Carlos
Differential regulation of transposable elements (TEs) during the murine submandibular gland development
title Differential regulation of transposable elements (TEs) during the murine submandibular gland development
title_full Differential regulation of transposable elements (TEs) during the murine submandibular gland development
title_fullStr Differential regulation of transposable elements (TEs) during the murine submandibular gland development
title_full_unstemmed Differential regulation of transposable elements (TEs) during the murine submandibular gland development
title_short Differential regulation of transposable elements (TEs) during the murine submandibular gland development
title_sort differential regulation of transposable elements (tes) during the murine submandibular gland development
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540199/
https://www.ncbi.nlm.nih.gov/pubmed/34686213
http://dx.doi.org/10.1186/s13100-021-00251-1
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