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Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy
Circular RNAs (circRNAs) regulate mRNA translation by binding to microRNAs (miRNAs), and their expression is altered in diverse disorders, including cancer, cardiovascular disease, and Parkinson’s disease. Here, we compare circRNA expression patterns in the temporal cortex and hippocampus of patient...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546880/ https://www.ncbi.nlm.nih.gov/pubmed/33101384 http://dx.doi.org/10.3389/fgene.2020.564301 |
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author | Gray, Lachlan G. Mills, James D. Curry-Hyde, Ashton Devore, Sasha Friedman, Daniel Thom, Maria Scott, Catherine Thijs, Roland D. Aronica, Eleonora Devinsky, Orrin Janitz, Michael |
author_facet | Gray, Lachlan G. Mills, James D. Curry-Hyde, Ashton Devore, Sasha Friedman, Daniel Thom, Maria Scott, Catherine Thijs, Roland D. Aronica, Eleonora Devinsky, Orrin Janitz, Michael |
author_sort | Gray, Lachlan G. |
collection | PubMed |
description | Circular RNAs (circRNAs) regulate mRNA translation by binding to microRNAs (miRNAs), and their expression is altered in diverse disorders, including cancer, cardiovascular disease, and Parkinson’s disease. Here, we compare circRNA expression patterns in the temporal cortex and hippocampus of patients with pharmacoresistant mesial temporal lobe epilepsy (MTLE) and healthy controls. Nine circRNAs showed significant differential expression, including circRNA-HOMER1, which is expressed in synapses. Further, we identified miRNA binding sites within the sequences of differentially expressed (DE) circRNAs; expression levels of mRNAs correlated with changes in complementary miRNAs. Gene set enrichment analysis of mRNA targets revealed functions in heterocyclic compound binding, regulation of transcription, and signal transduction, which maintain the structure and function of hippocampal neurons. The circRNA–miRNA–mRNA interaction networks illuminate the molecular changes in MTLE, which may be pathogenic or an effect of the disease or treatments and suggests that DE circRNAs and associated miRNAs may be novel therapeutic targets. |
format | Online Article Text |
id | pubmed-7546880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75468802020-10-22 Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy Gray, Lachlan G. Mills, James D. Curry-Hyde, Ashton Devore, Sasha Friedman, Daniel Thom, Maria Scott, Catherine Thijs, Roland D. Aronica, Eleonora Devinsky, Orrin Janitz, Michael Front Genet Genetics Circular RNAs (circRNAs) regulate mRNA translation by binding to microRNAs (miRNAs), and their expression is altered in diverse disorders, including cancer, cardiovascular disease, and Parkinson’s disease. Here, we compare circRNA expression patterns in the temporal cortex and hippocampus of patients with pharmacoresistant mesial temporal lobe epilepsy (MTLE) and healthy controls. Nine circRNAs showed significant differential expression, including circRNA-HOMER1, which is expressed in synapses. Further, we identified miRNA binding sites within the sequences of differentially expressed (DE) circRNAs; expression levels of mRNAs correlated with changes in complementary miRNAs. Gene set enrichment analysis of mRNA targets revealed functions in heterocyclic compound binding, regulation of transcription, and signal transduction, which maintain the structure and function of hippocampal neurons. The circRNA–miRNA–mRNA interaction networks illuminate the molecular changes in MTLE, which may be pathogenic or an effect of the disease or treatments and suggests that DE circRNAs and associated miRNAs may be novel therapeutic targets. Frontiers Media S.A. 2020-09-25 /pmc/articles/PMC7546880/ /pubmed/33101384 http://dx.doi.org/10.3389/fgene.2020.564301 Text en Copyright © 2020 Gray, Mills, Curry-Hyde, Devore, Friedman, Thom, Scott, Thijs, Aronica, Devinsky and Janitz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Gray, Lachlan G. Mills, James D. Curry-Hyde, Ashton Devore, Sasha Friedman, Daniel Thom, Maria Scott, Catherine Thijs, Roland D. Aronica, Eleonora Devinsky, Orrin Janitz, Michael Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy |
title | Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy |
title_full | Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy |
title_fullStr | Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy |
title_full_unstemmed | Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy |
title_short | Identification of Specific Circular RNA Expression Patterns and MicroRNA Interaction Networks in Mesial Temporal Lobe Epilepsy |
title_sort | identification of specific circular rna expression patterns and microrna interaction networks in mesial temporal lobe epilepsy |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546880/ https://www.ncbi.nlm.nih.gov/pubmed/33101384 http://dx.doi.org/10.3389/fgene.2020.564301 |
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