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Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation

Transposable elements cause alternative splicing (AS) in different ways, contributing to transcript diversification. Alternative polyadenylation (APA), one of the AS events, is related to the generation of mRNA isoforms in 70% of human genes. In this study, we tried to investigate AluYRa1s located a...

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Autores principales: Cho, Hyeon-Mu, Choe, Se-Hee, Kim, Young-Hyun, Park, Hye-Ri, Lee, Hee-Eun, Lee, Ja-Rang, Park, Sang-Je, Huh, Jae-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878741/
https://www.ncbi.nlm.nih.gov/pubmed/33574427
http://dx.doi.org/10.1038/s41598-021-83360-4
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author Cho, Hyeon-Mu
Choe, Se-Hee
Kim, Young-Hyun
Park, Hye-Ri
Lee, Hee-Eun
Lee, Ja-Rang
Park, Sang-Je
Huh, Jae-Won
author_facet Cho, Hyeon-Mu
Choe, Se-Hee
Kim, Young-Hyun
Park, Hye-Ri
Lee, Hee-Eun
Lee, Ja-Rang
Park, Sang-Je
Huh, Jae-Won
author_sort Cho, Hyeon-Mu
collection PubMed
description Transposable elements cause alternative splicing (AS) in different ways, contributing to transcript diversification. Alternative polyadenylation (APA), one of the AS events, is related to the generation of mRNA isoforms in 70% of human genes. In this study, we tried to investigate AluYRa1s located at the terminal region of cynomolgus monkey genes, utilizing both computational analysis and molecular experimentation. We found that ten genes had AluYRa1 at their 3′ end, and nine of these AluYRa1s were sense-oriented. Furthermore, in seven genes, AluYRa1s were expected to have a similar consensus sequence for polyadenylation cleavage. Additional computational analysis using the annotation files from the UCSC database showed that AluYRa1 was more involved in polyadenylation than in open reading frame exon splicing. To examine the extent of AluYRa1 involvement in polyadenylation, RNA-seq data from 30 normal cynomolgus monkeys were analyzed using TAPAS, a recently devised software that detects all the promising polyadenylation sites including APA sites. We observed that approximately 74% of possible polyadenylation sites in the analyzed genes were provided by sense-oriented AluYRa1. In conclusion, AluYRa1 is an Old-World monkey-specific TE, and its sense-oriented insertion at the 3′UTR region tends to provide a favorable environment for polyadenylation, diversifying gene transcripts.
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spelling pubmed-78787412021-02-12 Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation Cho, Hyeon-Mu Choe, Se-Hee Kim, Young-Hyun Park, Hye-Ri Lee, Hee-Eun Lee, Ja-Rang Park, Sang-Je Huh, Jae-Won Sci Rep Article Transposable elements cause alternative splicing (AS) in different ways, contributing to transcript diversification. Alternative polyadenylation (APA), one of the AS events, is related to the generation of mRNA isoforms in 70% of human genes. In this study, we tried to investigate AluYRa1s located at the terminal region of cynomolgus monkey genes, utilizing both computational analysis and molecular experimentation. We found that ten genes had AluYRa1 at their 3′ end, and nine of these AluYRa1s were sense-oriented. Furthermore, in seven genes, AluYRa1s were expected to have a similar consensus sequence for polyadenylation cleavage. Additional computational analysis using the annotation files from the UCSC database showed that AluYRa1 was more involved in polyadenylation than in open reading frame exon splicing. To examine the extent of AluYRa1 involvement in polyadenylation, RNA-seq data from 30 normal cynomolgus monkeys were analyzed using TAPAS, a recently devised software that detects all the promising polyadenylation sites including APA sites. We observed that approximately 74% of possible polyadenylation sites in the analyzed genes were provided by sense-oriented AluYRa1. In conclusion, AluYRa1 is an Old-World monkey-specific TE, and its sense-oriented insertion at the 3′UTR region tends to provide a favorable environment for polyadenylation, diversifying gene transcripts. Nature Publishing Group UK 2021-02-11 /pmc/articles/PMC7878741/ /pubmed/33574427 http://dx.doi.org/10.1038/s41598-021-83360-4 Text en © The Author(s) 2021 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/.
spellingShingle Article
Cho, Hyeon-Mu
Choe, Se-Hee
Kim, Young-Hyun
Park, Hye-Ri
Lee, Hee-Eun
Lee, Ja-Rang
Park, Sang-Je
Huh, Jae-Won
Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation
title Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation
title_full Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation
title_fullStr Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation
title_full_unstemmed Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation
title_short Sense-oriented AluYRa1 elements provide a lineage-specific transcription environment for polyadenylation
title_sort sense-oriented aluyra1 elements provide a lineage-specific transcription environment for polyadenylation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878741/
https://www.ncbi.nlm.nih.gov/pubmed/33574427
http://dx.doi.org/10.1038/s41598-021-83360-4
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