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Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers
Myocardium transcriptomes of left and right atria and ventricles from four adult male C57Bl/6j mice were profiled with Agilent microarrays to identify the differences responsible for the distinct functional roles of the four heart chambers. Female mice were not investigated owing to their transcript...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854717/ https://www.ncbi.nlm.nih.gov/pubmed/33531573 http://dx.doi.org/10.1038/s41598-021-82383-1 |
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author | Iacobas, Sanda Amuzescu, Bogdan Iacobas, Dumitru A. |
author_facet | Iacobas, Sanda Amuzescu, Bogdan Iacobas, Dumitru A. |
author_sort | Iacobas, Sanda |
collection | PubMed |
description | Myocardium transcriptomes of left and right atria and ventricles from four adult male C57Bl/6j mice were profiled with Agilent microarrays to identify the differences responsible for the distinct functional roles of the four heart chambers. Female mice were not investigated owing to their transcriptome dependence on the estrous cycle phase. Out of the quantified 16,886 unigenes, 15.76% on the left side and 16.5% on the right side exhibited differential expression between the atrium and the ventricle, while 5.8% of genes were differently expressed between the two atria and only 1.2% between the two ventricles. The study revealed also chamber differences in gene expression control and coordination. We analyzed ion channels and transporters, and genes within the cardiac muscle contraction, oxidative phosphorylation, glycolysis/gluconeogenesis, calcium and adrenergic signaling pathways. Interestingly, while expression of Ank2 oscillates in phase with all 27 quantified binding partners in the left ventricle, the percentage of in-phase oscillating partners of Ank2 is 15% and 37% in the left and right atria and 74% in the right ventricle. The analysis indicated high interventricular synchrony of the ion channels expressions and the substantially lower synchrony between the two atria and between the atrium and the ventricle from the same side. |
format | Online Article Text |
id | pubmed-7854717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78547172021-02-03 Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers Iacobas, Sanda Amuzescu, Bogdan Iacobas, Dumitru A. Sci Rep Article Myocardium transcriptomes of left and right atria and ventricles from four adult male C57Bl/6j mice were profiled with Agilent microarrays to identify the differences responsible for the distinct functional roles of the four heart chambers. Female mice were not investigated owing to their transcriptome dependence on the estrous cycle phase. Out of the quantified 16,886 unigenes, 15.76% on the left side and 16.5% on the right side exhibited differential expression between the atrium and the ventricle, while 5.8% of genes were differently expressed between the two atria and only 1.2% between the two ventricles. The study revealed also chamber differences in gene expression control and coordination. We analyzed ion channels and transporters, and genes within the cardiac muscle contraction, oxidative phosphorylation, glycolysis/gluconeogenesis, calcium and adrenergic signaling pathways. Interestingly, while expression of Ank2 oscillates in phase with all 27 quantified binding partners in the left ventricle, the percentage of in-phase oscillating partners of Ank2 is 15% and 37% in the left and right atria and 74% in the right ventricle. The analysis indicated high interventricular synchrony of the ion channels expressions and the substantially lower synchrony between the two atria and between the atrium and the ventricle from the same side. Nature Publishing Group UK 2021-02-02 /pmc/articles/PMC7854717/ /pubmed/33531573 http://dx.doi.org/10.1038/s41598-021-82383-1 Text en © The Author(s) 2021 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 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/. |
spellingShingle | Article Iacobas, Sanda Amuzescu, Bogdan Iacobas, Dumitru A. Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
title | Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
title_full | Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
title_fullStr | Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
title_full_unstemmed | Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
title_short | Transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
title_sort | transcriptomic uniqueness and commonality of the ion channels and transporters in the four heart chambers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854717/ https://www.ncbi.nlm.nih.gov/pubmed/33531573 http://dx.doi.org/10.1038/s41598-021-82383-1 |
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