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Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons

Transcriptional responses to the appropriate temporal pattern of action potential firing are essential for long-term adaption of neuronal properties to the functional activity of neural circuits and environmental experience. However, standard transcriptome analysis methods can be too limited in iden...

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Autores principales: Iacobas, Dumitru A., Iacobas, Sanda, Lee, Philip R., Cohen, Jonathan E., Fields, R. Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826514/
https://www.ncbi.nlm.nih.gov/pubmed/31561430
http://dx.doi.org/10.3390/genes10100754
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author Iacobas, Dumitru A.
Iacobas, Sanda
Lee, Philip R.
Cohen, Jonathan E.
Fields, R. Douglas
author_facet Iacobas, Dumitru A.
Iacobas, Sanda
Lee, Philip R.
Cohen, Jonathan E.
Fields, R. Douglas
author_sort Iacobas, Dumitru A.
collection PubMed
description Transcriptional responses to the appropriate temporal pattern of action potential firing are essential for long-term adaption of neuronal properties to the functional activity of neural circuits and environmental experience. However, standard transcriptome analysis methods can be too limited in identifying critical aspects that coordinate temporal coding of action potential firing with transcriptome response. A Pearson correlation analysis was applied to determine how pairs of genes in the mouse dorsal root ganglion (DRG) neurons are coordinately expressed in response to stimulation producing the same number of action potentials by two different temporal patterns. Analysis of 4728 distinct gene-pairs related to calcium signaling, 435,711 pairs of transcription factors, 820 pairs of voltage-gated ion channels, and 86,862 pairs of calcium signaling genes with transcription factors indicated that genes become coordinately activated by distinct action potential firing patterns and this depends on the duration of stimulation. Moreover, a measure of expression variance revealed that the control of transcripts abundances is sensitive to the pattern of stimulation. Thus, action potentials impact intracellular signaling and the transcriptome in dynamic manner that not only alter gene expression levels significantly (as previously reported) but also affects the control of their expression fluctuations and profoundly remodel the transcriptional networks.
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spelling pubmed-68265142019-11-18 Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons Iacobas, Dumitru A. Iacobas, Sanda Lee, Philip R. Cohen, Jonathan E. Fields, R. Douglas Genes (Basel) Article Transcriptional responses to the appropriate temporal pattern of action potential firing are essential for long-term adaption of neuronal properties to the functional activity of neural circuits and environmental experience. However, standard transcriptome analysis methods can be too limited in identifying critical aspects that coordinate temporal coding of action potential firing with transcriptome response. A Pearson correlation analysis was applied to determine how pairs of genes in the mouse dorsal root ganglion (DRG) neurons are coordinately expressed in response to stimulation producing the same number of action potentials by two different temporal patterns. Analysis of 4728 distinct gene-pairs related to calcium signaling, 435,711 pairs of transcription factors, 820 pairs of voltage-gated ion channels, and 86,862 pairs of calcium signaling genes with transcription factors indicated that genes become coordinately activated by distinct action potential firing patterns and this depends on the duration of stimulation. Moreover, a measure of expression variance revealed that the control of transcripts abundances is sensitive to the pattern of stimulation. Thus, action potentials impact intracellular signaling and the transcriptome in dynamic manner that not only alter gene expression levels significantly (as previously reported) but also affects the control of their expression fluctuations and profoundly remodel the transcriptional networks. MDPI 2019-09-26 /pmc/articles/PMC6826514/ /pubmed/31561430 http://dx.doi.org/10.3390/genes10100754 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Iacobas, Dumitru A.
Iacobas, Sanda
Lee, Philip R.
Cohen, Jonathan E.
Fields, R. Douglas
Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons
title Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons
title_full Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons
title_fullStr Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons
title_full_unstemmed Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons
title_short Coordinated Activity of Transcriptional Networks Responding to the Pattern of Action Potential Firing in Neurons
title_sort coordinated activity of transcriptional networks responding to the pattern of action potential firing in neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826514/
https://www.ncbi.nlm.nih.gov/pubmed/31561430
http://dx.doi.org/10.3390/genes10100754
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