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Dynamic landscape of tandem 3′ UTRs during zebrafish development
Tandem 3′ untranslated regions (UTRs), produced by alternative polyadenylation (APA) in the terminal exon of a gene, could have critical roles in regulating gene networks. Here we profiled tandem poly(A) events on a genome-wide scale during the embryonic development of zebrafish (Danio rerio) using...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460185/ https://www.ncbi.nlm.nih.gov/pubmed/22955139 http://dx.doi.org/10.1101/gr.128488.111 |
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author | Li, Yuxin Sun, Yu Fu, Yonggui Li, Mengzhen Huang, Guangrui Zhang, Chenxu Liang, Jiahui Huang, Shengfeng Shen, Gaoyang Yuan, Shaochun Chen, Liangfu Chen, Shangwu Xu, Anlong |
author_facet | Li, Yuxin Sun, Yu Fu, Yonggui Li, Mengzhen Huang, Guangrui Zhang, Chenxu Liang, Jiahui Huang, Shengfeng Shen, Gaoyang Yuan, Shaochun Chen, Liangfu Chen, Shangwu Xu, Anlong |
author_sort | Li, Yuxin |
collection | PubMed |
description | Tandem 3′ untranslated regions (UTRs), produced by alternative polyadenylation (APA) in the terminal exon of a gene, could have critical roles in regulating gene networks. Here we profiled tandem poly(A) events on a genome-wide scale during the embryonic development of zebrafish (Danio rerio) using a recently developed SAPAS method. We showed that 43% of the expressed protein-coding genes have tandem 3′ UTRs. The average 3′ UTR length follows a V-shaped dynamic pattern during early embryogenesis, in which the 3′ UTRs are first shortened at zygotic genome activation, and then quickly lengthened during gastrulation. Over 4000 genes are found to switch tandem APA sites, and the distinct functional roles of these genes are indicated by Gene Ontology analysis. Three families of cis-elements, including miR-430 seed, U-rich element, and canonical poly(A) signal, are enriched in 3′ UTR-shortened/lengthened genes in a stage-specific manner, suggesting temporal regulation coordinated by APA and trans-acting factors. Our results highlight the regulatory role of tandem 3′ UTR control in early embryogenesis and suggest that APA may represent a new epigenetic paradigm of physiological regulations. |
format | Online Article Text |
id | pubmed-3460185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34601852013-04-01 Dynamic landscape of tandem 3′ UTRs during zebrafish development Li, Yuxin Sun, Yu Fu, Yonggui Li, Mengzhen Huang, Guangrui Zhang, Chenxu Liang, Jiahui Huang, Shengfeng Shen, Gaoyang Yuan, Shaochun Chen, Liangfu Chen, Shangwu Xu, Anlong Genome Res Research Tandem 3′ untranslated regions (UTRs), produced by alternative polyadenylation (APA) in the terminal exon of a gene, could have critical roles in regulating gene networks. Here we profiled tandem poly(A) events on a genome-wide scale during the embryonic development of zebrafish (Danio rerio) using a recently developed SAPAS method. We showed that 43% of the expressed protein-coding genes have tandem 3′ UTRs. The average 3′ UTR length follows a V-shaped dynamic pattern during early embryogenesis, in which the 3′ UTRs are first shortened at zygotic genome activation, and then quickly lengthened during gastrulation. Over 4000 genes are found to switch tandem APA sites, and the distinct functional roles of these genes are indicated by Gene Ontology analysis. Three families of cis-elements, including miR-430 seed, U-rich element, and canonical poly(A) signal, are enriched in 3′ UTR-shortened/lengthened genes in a stage-specific manner, suggesting temporal regulation coordinated by APA and trans-acting factors. Our results highlight the regulatory role of tandem 3′ UTR control in early embryogenesis and suggest that APA may represent a new epigenetic paradigm of physiological regulations. Cold Spring Harbor Laboratory Press 2012-10 /pmc/articles/PMC3460185/ /pubmed/22955139 http://dx.doi.org/10.1101/gr.128488.111 Text en © 2012, Published by Cold Spring Harbor Laboratory Press This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/. |
spellingShingle | Research Li, Yuxin Sun, Yu Fu, Yonggui Li, Mengzhen Huang, Guangrui Zhang, Chenxu Liang, Jiahui Huang, Shengfeng Shen, Gaoyang Yuan, Shaochun Chen, Liangfu Chen, Shangwu Xu, Anlong Dynamic landscape of tandem 3′ UTRs during zebrafish development |
title | Dynamic landscape of tandem 3′ UTRs during zebrafish development |
title_full | Dynamic landscape of tandem 3′ UTRs during zebrafish development |
title_fullStr | Dynamic landscape of tandem 3′ UTRs during zebrafish development |
title_full_unstemmed | Dynamic landscape of tandem 3′ UTRs during zebrafish development |
title_short | Dynamic landscape of tandem 3′ UTRs during zebrafish development |
title_sort | dynamic landscape of tandem 3′ utrs during zebrafish development |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460185/ https://www.ncbi.nlm.nih.gov/pubmed/22955139 http://dx.doi.org/10.1101/gr.128488.111 |
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