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Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis
BACKGROUND: The development of the brain requires precise coordination of molecular processes across many cell-types. Underpinning these events are gene expression programs which require intricate regulation by non-coding regulatory sequences known as enhancers. In the context of the developing brai...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291752/ https://www.ncbi.nlm.nih.gov/pubmed/37365500 http://dx.doi.org/10.1186/s12864-023-09368-4 |
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author | Ramirez, Miguel Robert, Remi Yeung, Joanna Wu, Joshua Abdalla-Wyse, Ayasha Goldowitz, Daniel |
author_facet | Ramirez, Miguel Robert, Remi Yeung, Joanna Wu, Joshua Abdalla-Wyse, Ayasha Goldowitz, Daniel |
author_sort | Ramirez, Miguel |
collection | PubMed |
description | BACKGROUND: The development of the brain requires precise coordination of molecular processes across many cell-types. Underpinning these events are gene expression programs which require intricate regulation by non-coding regulatory sequences known as enhancers. In the context of the developing brain, transcribed enhancers (TEs) regulate temporally-specific expression of genes critical for cell identity and differentiation. Transcription of non-coding RNAs at active enhancer sequences, known as enhancer RNAs (eRNAs), is tightly associated with enhancer activity and has been correlated with target gene expression. TEs have been characterized in a multitude of developing tissues, however their regulatory role has yet to be described in the context of embryonic and early postnatal brain development. In this study, eRNA transcription was analyzed to identify TEs active during cerebellar development, as a proxy for the developing brain. Cap Analysis of Gene Expression followed by sequencing (CAGE-seq) was conducted at 12 stages throughout embryonic and early postnatal cerebellar development. RESULTS: Temporal analysis of eRNA transcription identified clusters of TEs that peak in activity during either embryonic or postnatal times, highlighting their importance for temporally specific developmental events. Functional analysis of putative target genes identified molecular mechanisms under TE regulation revealing that TEs regulate genes involved in biological processes specific to neurons. We validate enhancer activity using in situ hybridization of eRNA expression from TEs predicted to regulate Nfib, a gene critical for cerebellar granule cell differentiation. CONCLUSIONS: The results of this analysis provide a valuable dataset for the identification of cerebellar enhancers and provide insight into the molecular mechanisms critical for brain development under TE regulation. This dataset is shared with the community through an online resource (https://goldowitzlab.shinyapps.io/trans-enh-app/). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09368-4. |
format | Online Article Text |
id | pubmed-10291752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102917522023-06-27 Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis Ramirez, Miguel Robert, Remi Yeung, Joanna Wu, Joshua Abdalla-Wyse, Ayasha Goldowitz, Daniel BMC Genomics Research BACKGROUND: The development of the brain requires precise coordination of molecular processes across many cell-types. Underpinning these events are gene expression programs which require intricate regulation by non-coding regulatory sequences known as enhancers. In the context of the developing brain, transcribed enhancers (TEs) regulate temporally-specific expression of genes critical for cell identity and differentiation. Transcription of non-coding RNAs at active enhancer sequences, known as enhancer RNAs (eRNAs), is tightly associated with enhancer activity and has been correlated with target gene expression. TEs have been characterized in a multitude of developing tissues, however their regulatory role has yet to be described in the context of embryonic and early postnatal brain development. In this study, eRNA transcription was analyzed to identify TEs active during cerebellar development, as a proxy for the developing brain. Cap Analysis of Gene Expression followed by sequencing (CAGE-seq) was conducted at 12 stages throughout embryonic and early postnatal cerebellar development. RESULTS: Temporal analysis of eRNA transcription identified clusters of TEs that peak in activity during either embryonic or postnatal times, highlighting their importance for temporally specific developmental events. Functional analysis of putative target genes identified molecular mechanisms under TE regulation revealing that TEs regulate genes involved in biological processes specific to neurons. We validate enhancer activity using in situ hybridization of eRNA expression from TEs predicted to regulate Nfib, a gene critical for cerebellar granule cell differentiation. CONCLUSIONS: The results of this analysis provide a valuable dataset for the identification of cerebellar enhancers and provide insight into the molecular mechanisms critical for brain development under TE regulation. This dataset is shared with the community through an online resource (https://goldowitzlab.shinyapps.io/trans-enh-app/). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09368-4. BioMed Central 2023-06-26 /pmc/articles/PMC10291752/ /pubmed/37365500 http://dx.doi.org/10.1186/s12864-023-09368-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ramirez, Miguel Robert, Remi Yeung, Joanna Wu, Joshua Abdalla-Wyse, Ayasha Goldowitz, Daniel Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis |
title | Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis |
title_full | Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis |
title_fullStr | Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis |
title_full_unstemmed | Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis |
title_short | Identification and characterization of transcribed enhancers during cerebellar development through enhancer RNA analysis |
title_sort | identification and characterization of transcribed enhancers during cerebellar development through enhancer rna analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291752/ https://www.ncbi.nlm.nih.gov/pubmed/37365500 http://dx.doi.org/10.1186/s12864-023-09368-4 |
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