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Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties

BACKGROUND: Stable introns and intronic fragments make up the largest population of RNA in the oocyte nucleus of the frog Xenopus tropicalis. These stable intronic sequence RNAs (sisRNAs) persist through the onset of zygotic transcription when synchronous cell division has ended, and the developing...

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Autores principales: Jin, Jing, He, Ximiao, Silva, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137253/
https://www.ncbi.nlm.nih.gov/pubmed/32264855
http://dx.doi.org/10.1186/s12864-020-6687-9
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author Jin, Jing
He, Ximiao
Silva, Elena
author_facet Jin, Jing
He, Ximiao
Silva, Elena
author_sort Jin, Jing
collection PubMed
description BACKGROUND: Stable introns and intronic fragments make up the largest population of RNA in the oocyte nucleus of the frog Xenopus tropicalis. These stable intronic sequence RNAs (sisRNAs) persist through the onset of zygotic transcription when synchronous cell division has ended, and the developing embryo consists of approximately 8000 cells. Despite their abundance, the sequence properties and biological function of sisRNAs are just beginning to be understood. RESULTS: To characterize this population of non-coding RNA, we identified all of the sisRNAs in the X. tropicalis oocyte nucleus using published high-throughput RNA sequencing data. Our analysis revealed that sisRNAs, have an average length of ~ 360 nt, are widely expressed from genes with multiple introns, and are derived from specific regions of introns that are GC and TG rich, while CpG poor. They are enriched in introns at both ends of transcripts but preferentially at the 3′ end. The consensus binding sites of specific transcription factors such as Stat3 are enriched in sisRNAs, suggesting an association between sisRNAs and transcription factors involved in early development. Evolutionary conservation analysis of sisRNA sequences in seven vertebrate genomes indicates that sisRNAs are as conserved as other parts of introns, but much less conserved than exons. CONCLUSION: In total, our results indicate sisRNAs are selected intron regions with distinct properties and may play a role in gene expression regulation.
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spelling pubmed-71372532020-04-11 Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties Jin, Jing He, Ximiao Silva, Elena BMC Genomics Research Article BACKGROUND: Stable introns and intronic fragments make up the largest population of RNA in the oocyte nucleus of the frog Xenopus tropicalis. These stable intronic sequence RNAs (sisRNAs) persist through the onset of zygotic transcription when synchronous cell division has ended, and the developing embryo consists of approximately 8000 cells. Despite their abundance, the sequence properties and biological function of sisRNAs are just beginning to be understood. RESULTS: To characterize this population of non-coding RNA, we identified all of the sisRNAs in the X. tropicalis oocyte nucleus using published high-throughput RNA sequencing data. Our analysis revealed that sisRNAs, have an average length of ~ 360 nt, are widely expressed from genes with multiple introns, and are derived from specific regions of introns that are GC and TG rich, while CpG poor. They are enriched in introns at both ends of transcripts but preferentially at the 3′ end. The consensus binding sites of specific transcription factors such as Stat3 are enriched in sisRNAs, suggesting an association between sisRNAs and transcription factors involved in early development. Evolutionary conservation analysis of sisRNA sequences in seven vertebrate genomes indicates that sisRNAs are as conserved as other parts of introns, but much less conserved than exons. CONCLUSION: In total, our results indicate sisRNAs are selected intron regions with distinct properties and may play a role in gene expression regulation. BioMed Central 2020-04-07 /pmc/articles/PMC7137253/ /pubmed/32264855 http://dx.doi.org/10.1186/s12864-020-6687-9 Text en © The Author(s). 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Jin, Jing
He, Ximiao
Silva, Elena
Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties
title Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties
title_full Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties
title_fullStr Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties
title_full_unstemmed Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties
title_short Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties
title_sort stable intronic sequence rnas (sisrnas) are selected regions in introns with distinct properties
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137253/
https://www.ncbi.nlm.nih.gov/pubmed/32264855
http://dx.doi.org/10.1186/s12864-020-6687-9
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