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Identification of cell states using super-enhancer RNA
BACKGROUND: A new class of regulatory elements called super-enhancers, comprised of multiple neighboring enhancers, have recently been reported to be the key transcriptional drivers of cellular, developmental, and disease states. RESULTS: Here, we defined super-enhancer RNAs as highly expressed enha...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564956/ https://www.ncbi.nlm.nih.gov/pubmed/34727867 http://dx.doi.org/10.1186/s12864-021-08092-1 |
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author | Tu, Yueh-Hua Juan, Hsueh-Fen Huang, Hsuan-Cheng |
author_facet | Tu, Yueh-Hua Juan, Hsueh-Fen Huang, Hsuan-Cheng |
author_sort | Tu, Yueh-Hua |
collection | PubMed |
description | BACKGROUND: A new class of regulatory elements called super-enhancers, comprised of multiple neighboring enhancers, have recently been reported to be the key transcriptional drivers of cellular, developmental, and disease states. RESULTS: Here, we defined super-enhancer RNAs as highly expressed enhancer RNAs that are transcribed from a cluster of localized genomic regions. Using the cap analysis of gene expression sequencing data from FANTOM5, we systematically explored the enhancer and messenger RNA landscapes in hundreds of different cell types in response to various environments. Applying non-negative matrix factorization (NMF) to super-enhancer RNA profiles, we found that different cell types were well classified. In addition, through the NMF of individual time-course profiles from a single cell-type, super-enhancer RNAs were clustered into several states with progressive patterns. We further investigated the enriched biological functions of the proximal genes involved in each pattern, and found that they were associated with the corresponding developmental process. CONCLUSIONS: The proposed super-enhancer RNAs can act as a good alternative, without the complicated measurement of histone modifications, for identifying important regulatory elements of cell type specification and identifying dynamic cell states. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08092-1. |
format | Online Article Text |
id | pubmed-8564956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85649562021-11-04 Identification of cell states using super-enhancer RNA Tu, Yueh-Hua Juan, Hsueh-Fen Huang, Hsuan-Cheng BMC Genomics Research BACKGROUND: A new class of regulatory elements called super-enhancers, comprised of multiple neighboring enhancers, have recently been reported to be the key transcriptional drivers of cellular, developmental, and disease states. RESULTS: Here, we defined super-enhancer RNAs as highly expressed enhancer RNAs that are transcribed from a cluster of localized genomic regions. Using the cap analysis of gene expression sequencing data from FANTOM5, we systematically explored the enhancer and messenger RNA landscapes in hundreds of different cell types in response to various environments. Applying non-negative matrix factorization (NMF) to super-enhancer RNA profiles, we found that different cell types were well classified. In addition, through the NMF of individual time-course profiles from a single cell-type, super-enhancer RNAs were clustered into several states with progressive patterns. We further investigated the enriched biological functions of the proximal genes involved in each pattern, and found that they were associated with the corresponding developmental process. CONCLUSIONS: The proposed super-enhancer RNAs can act as a good alternative, without the complicated measurement of histone modifications, for identifying important regulatory elements of cell type specification and identifying dynamic cell states. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08092-1. BioMed Central 2021-11-02 /pmc/articles/PMC8564956/ /pubmed/34727867 http://dx.doi.org/10.1186/s12864-021-08092-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Tu, Yueh-Hua Juan, Hsueh-Fen Huang, Hsuan-Cheng Identification of cell states using super-enhancer RNA |
title | Identification of cell states using super-enhancer RNA |
title_full | Identification of cell states using super-enhancer RNA |
title_fullStr | Identification of cell states using super-enhancer RNA |
title_full_unstemmed | Identification of cell states using super-enhancer RNA |
title_short | Identification of cell states using super-enhancer RNA |
title_sort | identification of cell states using super-enhancer rna |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564956/ https://www.ncbi.nlm.nih.gov/pubmed/34727867 http://dx.doi.org/10.1186/s12864-021-08092-1 |
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