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Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit
BACKGROUND: Adult neurogenesis and the incorporation of adult-born neurons into functional circuits requires precise spatiotemporal coordination across molecular networks regulating a wide array of processes, including cell proliferation, apoptosis, neurotrophin signaling, and electrical activity. M...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636775/ https://www.ncbi.nlm.nih.gov/pubmed/26545368 http://dx.doi.org/10.1186/s12864-015-2175-z |
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author | Larson, Tracy A. Lent, Karin L. Bammler, Theo K. MacDonald, James W. Wood, William E. Caras, Melissa L. Thatra, Nivretta M. Budzillo, Agata Perkel, David J. Brenowitz, Eliot A. |
author_facet | Larson, Tracy A. Lent, Karin L. Bammler, Theo K. MacDonald, James W. Wood, William E. Caras, Melissa L. Thatra, Nivretta M. Budzillo, Agata Perkel, David J. Brenowitz, Eliot A. |
author_sort | Larson, Tracy A. |
collection | PubMed |
description | BACKGROUND: Adult neurogenesis and the incorporation of adult-born neurons into functional circuits requires precise spatiotemporal coordination across molecular networks regulating a wide array of processes, including cell proliferation, apoptosis, neurotrophin signaling, and electrical activity. MicroRNAs (miRs) - short, non-coding RNA sequences that alter gene expression by post-transcriptional inhibition or degradation of mRNA sequences - may be involved in the global coordination of such diverse biological processes. To test the hypothesis that miRs related to adult neurogenesis and related cellular processes are functionally regulated in the nuclei of the avian song control circuit, we used microarray analyses to quantify changes in expression of miRs and predicted target mRNAs in the telencephalic nuclei HVC, the robust nucleus of arcopallium (RA), and the basal ganglia homologue Area X in breeding and nonbreeding Gambel’s white-crowned sparrows (Zonotrichia leucophrys gambelli). RESULTS: We identified 46 different miRs that were differentially expressed across seasons in the song nuclei. miR-132 and miR-210 showed the highest differential expression in HVC and Area X, respectively. Analyzing predicted mRNA targets of miR-132 identified 33 candidate target genes that regulate processes including cell cycle control, calcium signaling, and neuregulin signaling in HVC. Likewise, miR-210 was predicted to target 14 mRNAs differentially expressed across seasons that regulate serotonin, GABA, and dopamine receptor signaling and inflammation. CONCLUSIONS: Our results identify potential miR–mRNA regulatory networks related to adult neurogenesis and provide opportunities to discover novel genetic control of the diverse biological processes and factors related to the functional incorporation of new neurons to the adult brain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2175-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4636775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46367752015-11-08 Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit Larson, Tracy A. Lent, Karin L. Bammler, Theo K. MacDonald, James W. Wood, William E. Caras, Melissa L. Thatra, Nivretta M. Budzillo, Agata Perkel, David J. Brenowitz, Eliot A. BMC Genomics Research Article BACKGROUND: Adult neurogenesis and the incorporation of adult-born neurons into functional circuits requires precise spatiotemporal coordination across molecular networks regulating a wide array of processes, including cell proliferation, apoptosis, neurotrophin signaling, and electrical activity. MicroRNAs (miRs) - short, non-coding RNA sequences that alter gene expression by post-transcriptional inhibition or degradation of mRNA sequences - may be involved in the global coordination of such diverse biological processes. To test the hypothesis that miRs related to adult neurogenesis and related cellular processes are functionally regulated in the nuclei of the avian song control circuit, we used microarray analyses to quantify changes in expression of miRs and predicted target mRNAs in the telencephalic nuclei HVC, the robust nucleus of arcopallium (RA), and the basal ganglia homologue Area X in breeding and nonbreeding Gambel’s white-crowned sparrows (Zonotrichia leucophrys gambelli). RESULTS: We identified 46 different miRs that were differentially expressed across seasons in the song nuclei. miR-132 and miR-210 showed the highest differential expression in HVC and Area X, respectively. Analyzing predicted mRNA targets of miR-132 identified 33 candidate target genes that regulate processes including cell cycle control, calcium signaling, and neuregulin signaling in HVC. Likewise, miR-210 was predicted to target 14 mRNAs differentially expressed across seasons that regulate serotonin, GABA, and dopamine receptor signaling and inflammation. CONCLUSIONS: Our results identify potential miR–mRNA regulatory networks related to adult neurogenesis and provide opportunities to discover novel genetic control of the diverse biological processes and factors related to the functional incorporation of new neurons to the adult brain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2175-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-06 /pmc/articles/PMC4636775/ /pubmed/26545368 http://dx.doi.org/10.1186/s12864-015-2175-z Text en © Larson et al. 2015 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 Larson, Tracy A. Lent, Karin L. Bammler, Theo K. MacDonald, James W. Wood, William E. Caras, Melissa L. Thatra, Nivretta M. Budzillo, Agata Perkel, David J. Brenowitz, Eliot A. Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit |
title | Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit |
title_full | Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit |
title_fullStr | Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit |
title_full_unstemmed | Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit |
title_short | Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit |
title_sort | network analysis of microrna and mrna seasonal dynamics in a highly plastic sensorimotor neural circuit |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636775/ https://www.ncbi.nlm.nih.gov/pubmed/26545368 http://dx.doi.org/10.1186/s12864-015-2175-z |
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