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Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function
Micro-RNAs (miRNAs) are short, single-stranded, noncoding RNAs that are involved in the regulation of protein-coding genes at the level of messenger RNA (mRNA). They are involved in the regulation of numerous traits, including developmental timing, apoptosis, immune function, and neuronal developmen...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer New York
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755775/ https://www.ncbi.nlm.nih.gov/pubmed/18594913 http://dx.doi.org/10.1007/s00335-008-9116-y |
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author | Parsons, Michael J. Grimm, Christina H. Paya-Cano, Jose L. Sugden, Karen Nietfeld, Wilfried Lehrach, Hans Schalkwyk, Leonard C. |
author_facet | Parsons, Michael J. Grimm, Christina H. Paya-Cano, Jose L. Sugden, Karen Nietfeld, Wilfried Lehrach, Hans Schalkwyk, Leonard C. |
author_sort | Parsons, Michael J. |
collection | PubMed |
description | Micro-RNAs (miRNAs) are short, single-stranded, noncoding RNAs that are involved in the regulation of protein-coding genes at the level of messenger RNA (mRNA). They are involved in the regulation of numerous traits, including developmental timing, apoptosis, immune function, and neuronal development. To better understand how the expression of the miRNAs themselves is regulated, we looked for miRNA expression differences among four mouse inbred strains, A/J, BALB/cJ, C57BL/6J, and DBA/2J, in one tissue, the hippocampus. A total of 166 miRNA RT-PCR assays were used to screen RNA pools for each strain. Twenty miRNA species that were markedly different between strains were further investigated using eight individual samples per strain, and 11 miRNAs showed significant differences across strains (p < 0.05). This is the first observation of miRNA expression differences across inbred mice strains. We conducted an in silico correlation analysis of the expression of these differentially expressed miRNAs with phenotype data and mRNA expression to better characterise the effects of these miRNAs on both phenotype and the regulation of mRNA expression. This approach has allowed us to nominate miRNAs that have potential roles in anxiety, exploration, and learning and memory. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00335-008-9116-y) contains supplementary material, which is available to authorized users. |
format | Text |
id | pubmed-2755775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Springer New York |
record_format | MEDLINE/PubMed |
spelling | pubmed-27557752009-10-07 Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function Parsons, Michael J. Grimm, Christina H. Paya-Cano, Jose L. Sugden, Karen Nietfeld, Wilfried Lehrach, Hans Schalkwyk, Leonard C. Mamm Genome Article Micro-RNAs (miRNAs) are short, single-stranded, noncoding RNAs that are involved in the regulation of protein-coding genes at the level of messenger RNA (mRNA). They are involved in the regulation of numerous traits, including developmental timing, apoptosis, immune function, and neuronal development. To better understand how the expression of the miRNAs themselves is regulated, we looked for miRNA expression differences among four mouse inbred strains, A/J, BALB/cJ, C57BL/6J, and DBA/2J, in one tissue, the hippocampus. A total of 166 miRNA RT-PCR assays were used to screen RNA pools for each strain. Twenty miRNA species that were markedly different between strains were further investigated using eight individual samples per strain, and 11 miRNAs showed significant differences across strains (p < 0.05). This is the first observation of miRNA expression differences across inbred mice strains. We conducted an in silico correlation analysis of the expression of these differentially expressed miRNAs with phenotype data and mRNA expression to better characterise the effects of these miRNAs on both phenotype and the regulation of mRNA expression. This approach has allowed us to nominate miRNAs that have potential roles in anxiety, exploration, and learning and memory. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00335-008-9116-y) contains supplementary material, which is available to authorized users. Springer New York 2008-07-02 2008 /pmc/articles/PMC2755775/ /pubmed/18594913 http://dx.doi.org/10.1007/s00335-008-9116-y Text en © Springer Science+Business Media, LLC 2008 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License ( https://creativecommons.org/licenses/by-nc/2.0 (https://creativecommons.org/licenses/by-nc/2.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Article Parsons, Michael J. Grimm, Christina H. Paya-Cano, Jose L. Sugden, Karen Nietfeld, Wilfried Lehrach, Hans Schalkwyk, Leonard C. Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function |
title | Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function |
title_full | Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function |
title_fullStr | Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function |
title_full_unstemmed | Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function |
title_short | Using hippocampal microRNA expression differences between mouse inbred strains to characterise miRNA function |
title_sort | using hippocampal microrna expression differences between mouse inbred strains to characterise mirna function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755775/ https://www.ncbi.nlm.nih.gov/pubmed/18594913 http://dx.doi.org/10.1007/s00335-008-9116-y |
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