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CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system

microRNAs are short, noncoding RNAs that can regulate hundreds of targets and thus shape the expression landscape of a cell. Similar to mRNA, they often exhibit cell type enriched expression and serve to reinforce cellular identity. In tissue with high cellular complexity, such as the central nervou...

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Autores principales: Pomper, Nathan, Liu, Yating, Hoye, Mariah L., Dougherty, Joseph D., Miller, Timothy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080788/
https://www.ncbi.nlm.nih.gov/pubmed/32188880
http://dx.doi.org/10.1038/s41598-020-61307-5
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author Pomper, Nathan
Liu, Yating
Hoye, Mariah L.
Dougherty, Joseph D.
Miller, Timothy M.
author_facet Pomper, Nathan
Liu, Yating
Hoye, Mariah L.
Dougherty, Joseph D.
Miller, Timothy M.
author_sort Pomper, Nathan
collection PubMed
description microRNAs are short, noncoding RNAs that can regulate hundreds of targets and thus shape the expression landscape of a cell. Similar to mRNA, they often exhibit cell type enriched expression and serve to reinforce cellular identity. In tissue with high cellular complexity, such as the central nervous system (CNS), it is difficult to attribute microRNA changes to a particular cell type. To facilitate interpretation of microRNA studies in these tissues, we used previously generated data to develop a publicly accessible and user-friendly database to enable exploration of cell type enriched microRNA expression. We provide illustrations of how this database can be utilized as a reference as well as for hypothesis generation. First, we suggest a putative role for miR-21 in the microglial spinal injury response. Second, we highlight data indicating that differential microRNA expression, specifically miR-326, may in part explain regional differences in inflammatory cells. Finally, we show that miR-383 expression is enriched in cortical glutamatergic neurons, suggesting a unique role in these cells. These examples illustrate the database’s utility in guiding research towards unstudied regulators in the CNS. This novel resource will aid future research into microRNA-based regulatory mechanisms responsible for cellular phenotypes within the CNS.
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spelling pubmed-70807882020-03-23 CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system Pomper, Nathan Liu, Yating Hoye, Mariah L. Dougherty, Joseph D. Miller, Timothy M. Sci Rep Article microRNAs are short, noncoding RNAs that can regulate hundreds of targets and thus shape the expression landscape of a cell. Similar to mRNA, they often exhibit cell type enriched expression and serve to reinforce cellular identity. In tissue with high cellular complexity, such as the central nervous system (CNS), it is difficult to attribute microRNA changes to a particular cell type. To facilitate interpretation of microRNA studies in these tissues, we used previously generated data to develop a publicly accessible and user-friendly database to enable exploration of cell type enriched microRNA expression. We provide illustrations of how this database can be utilized as a reference as well as for hypothesis generation. First, we suggest a putative role for miR-21 in the microglial spinal injury response. Second, we highlight data indicating that differential microRNA expression, specifically miR-326, may in part explain regional differences in inflammatory cells. Finally, we show that miR-383 expression is enriched in cortical glutamatergic neurons, suggesting a unique role in these cells. These examples illustrate the database’s utility in guiding research towards unstudied regulators in the CNS. This novel resource will aid future research into microRNA-based regulatory mechanisms responsible for cellular phenotypes within the CNS. Nature Publishing Group UK 2020-03-18 /pmc/articles/PMC7080788/ /pubmed/32188880 http://dx.doi.org/10.1038/s41598-020-61307-5 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pomper, Nathan
Liu, Yating
Hoye, Mariah L.
Dougherty, Joseph D.
Miller, Timothy M.
CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system
title CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system
title_full CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system
title_fullStr CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system
title_full_unstemmed CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system
title_short CNS microRNA profiles: a database for cell type enriched microRNA expression across the mouse central nervous system
title_sort cns microrna profiles: a database for cell type enriched microrna expression across the mouse central nervous system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080788/
https://www.ncbi.nlm.nih.gov/pubmed/32188880
http://dx.doi.org/10.1038/s41598-020-61307-5
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