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Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons

The exposure of mouse embryos in utero and primary cortical neurons to ionizing radiation results in the P53-dependent activation of a subset of genes that is highly induced during brain development and neuronal maturation, a feature that these genes reportedly share with circular RNAs (circRNAs). I...

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Autores principales: Mbouombouo Mfossa, André Claude, Thekkekara Puthenparampil, Helene, Inalegwu, Auchi, Coolkens, Amelie, Baatout, Sarah, Benotmane, Mohammed A., Huylebroeck, Danny, Quintens, Roel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721538/
https://www.ncbi.nlm.nih.gov/pubmed/31357500
http://dx.doi.org/10.3390/cells8080778
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author Mbouombouo Mfossa, André Claude
Thekkekara Puthenparampil, Helene
Inalegwu, Auchi
Coolkens, Amelie
Baatout, Sarah
Benotmane, Mohammed A.
Huylebroeck, Danny
Quintens, Roel
author_facet Mbouombouo Mfossa, André Claude
Thekkekara Puthenparampil, Helene
Inalegwu, Auchi
Coolkens, Amelie
Baatout, Sarah
Benotmane, Mohammed A.
Huylebroeck, Danny
Quintens, Roel
author_sort Mbouombouo Mfossa, André Claude
collection PubMed
description The exposure of mouse embryos in utero and primary cortical neurons to ionizing radiation results in the P53-dependent activation of a subset of genes that is highly induced during brain development and neuronal maturation, a feature that these genes reportedly share with circular RNAs (circRNAs). Interestingly, some of these genes are predicted to express circular transcripts. In this study, we validated the abundance of the circular transcript variants of four P53 target genes (Pvt1, Ano3, Sec14l5, and Rnf169). These circular variants were overall more stable than their linear counterparts. They were furthermore highly enriched in the brain and their transcript levels continuously increase during subsequent developmental stages (from embryonic day 12 until adulthood), while no further increase could be observed for linear mRNAs beyond post-natal day 30. Finally, whereas radiation-induced expression of P53 target mRNAs peaks early after exposure, several of the circRNAs showed prolonged induction in irradiated embryonic mouse brain, primary mouse cortical neurons, and mouse blood. Together, our results indicate that the circRNAs from these P53 target genes are induced in response to radiation and they corroborate the findings that circRNAs may represent biomarkers of brain age. We also propose that they may be superior to mRNA as long-term biomarkers for radiation exposure.
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spelling pubmed-67215382019-09-10 Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons Mbouombouo Mfossa, André Claude Thekkekara Puthenparampil, Helene Inalegwu, Auchi Coolkens, Amelie Baatout, Sarah Benotmane, Mohammed A. Huylebroeck, Danny Quintens, Roel Cells Article The exposure of mouse embryos in utero and primary cortical neurons to ionizing radiation results in the P53-dependent activation of a subset of genes that is highly induced during brain development and neuronal maturation, a feature that these genes reportedly share with circular RNAs (circRNAs). Interestingly, some of these genes are predicted to express circular transcripts. In this study, we validated the abundance of the circular transcript variants of four P53 target genes (Pvt1, Ano3, Sec14l5, and Rnf169). These circular variants were overall more stable than their linear counterparts. They were furthermore highly enriched in the brain and their transcript levels continuously increase during subsequent developmental stages (from embryonic day 12 until adulthood), while no further increase could be observed for linear mRNAs beyond post-natal day 30. Finally, whereas radiation-induced expression of P53 target mRNAs peaks early after exposure, several of the circRNAs showed prolonged induction in irradiated embryonic mouse brain, primary mouse cortical neurons, and mouse blood. Together, our results indicate that the circRNAs from these P53 target genes are induced in response to radiation and they corroborate the findings that circRNAs may represent biomarkers of brain age. We also propose that they may be superior to mRNA as long-term biomarkers for radiation exposure. MDPI 2019-07-26 /pmc/articles/PMC6721538/ /pubmed/31357500 http://dx.doi.org/10.3390/cells8080778 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
Mbouombouo Mfossa, André Claude
Thekkekara Puthenparampil, Helene
Inalegwu, Auchi
Coolkens, Amelie
Baatout, Sarah
Benotmane, Mohammed A.
Huylebroeck, Danny
Quintens, Roel
Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons
title Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons
title_full Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons
title_fullStr Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons
title_full_unstemmed Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons
title_short Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons
title_sort exposure to ionizing radiation triggers prolonged changes in circular rna abundance in the embryonic mouse brain and primary neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721538/
https://www.ncbi.nlm.nih.gov/pubmed/31357500
http://dx.doi.org/10.3390/cells8080778
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