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Relatively frequent switching of transcription start sites during cerebellar development

BACKGROUND: Alternative transcription start site (TSS) usage plays important roles in transcriptional control of mammalian gene expression. The growing interest in alternative TSSs and their role in genome diversification spawned many single-gene studies on differential usages of tissue-specific or...

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Autores principales: Zhang, Peter, Dimont, Emmanuel, Ha, Thomas, Swanson, Douglas J., Hide, Winston, Goldowitz, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470264/
https://www.ncbi.nlm.nih.gov/pubmed/28610618
http://dx.doi.org/10.1186/s12864-017-3834-z
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author Zhang, Peter
Dimont, Emmanuel
Ha, Thomas
Swanson, Douglas J.
Hide, Winston
Goldowitz, Dan
author_facet Zhang, Peter
Dimont, Emmanuel
Ha, Thomas
Swanson, Douglas J.
Hide, Winston
Goldowitz, Dan
author_sort Zhang, Peter
collection PubMed
description BACKGROUND: Alternative transcription start site (TSS) usage plays important roles in transcriptional control of mammalian gene expression. The growing interest in alternative TSSs and their role in genome diversification spawned many single-gene studies on differential usages of tissue-specific or temporal-specific alternative TSSs. However, exploration of the switching usage of alternative TSS usage on a genomic level, especially in the central nervous system, is largely lacking. RESULTS: In this study, We have prepared a unique set of time-course data for the developing cerebellum, as part of the FANTOM5 consortium (http://fantom.gsc.riken.jp/5/) that uses their innovative capturing of 5′ ends of all transcripts followed by Helicos next generation sequencing. We analyzed the usage of all transcription start sites (TSSs) at each time point during cerebellar development that provided information on multiple RNA isoforms that emerged from the same gene. We developed a mathematical method that systematically compares the expression of different TSSs of a gene to identify temporal crossover and non-crossover switching events. We identified 48,489 novel TSS switching events in 5433 genes during cerebellar development. This includes 9767 crossover TSS switching events in 1511 genes, where the dominant TSS shifts over time. CONCLUSIONS: We observed a relatively high prevalence of TSS switching in cerebellar development where the resulting temporally-specific gene transcripts and protein products can play important regulatory and functional roles.
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spelling pubmed-54702642017-06-19 Relatively frequent switching of transcription start sites during cerebellar development Zhang, Peter Dimont, Emmanuel Ha, Thomas Swanson, Douglas J. Hide, Winston Goldowitz, Dan BMC Genomics Research Article BACKGROUND: Alternative transcription start site (TSS) usage plays important roles in transcriptional control of mammalian gene expression. The growing interest in alternative TSSs and their role in genome diversification spawned many single-gene studies on differential usages of tissue-specific or temporal-specific alternative TSSs. However, exploration of the switching usage of alternative TSS usage on a genomic level, especially in the central nervous system, is largely lacking. RESULTS: In this study, We have prepared a unique set of time-course data for the developing cerebellum, as part of the FANTOM5 consortium (http://fantom.gsc.riken.jp/5/) that uses their innovative capturing of 5′ ends of all transcripts followed by Helicos next generation sequencing. We analyzed the usage of all transcription start sites (TSSs) at each time point during cerebellar development that provided information on multiple RNA isoforms that emerged from the same gene. We developed a mathematical method that systematically compares the expression of different TSSs of a gene to identify temporal crossover and non-crossover switching events. We identified 48,489 novel TSS switching events in 5433 genes during cerebellar development. This includes 9767 crossover TSS switching events in 1511 genes, where the dominant TSS shifts over time. CONCLUSIONS: We observed a relatively high prevalence of TSS switching in cerebellar development where the resulting temporally-specific gene transcripts and protein products can play important regulatory and functional roles. BioMed Central 2017-06-13 /pmc/articles/PMC5470264/ /pubmed/28610618 http://dx.doi.org/10.1186/s12864-017-3834-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Zhang, Peter
Dimont, Emmanuel
Ha, Thomas
Swanson, Douglas J.
Hide, Winston
Goldowitz, Dan
Relatively frequent switching of transcription start sites during cerebellar development
title Relatively frequent switching of transcription start sites during cerebellar development
title_full Relatively frequent switching of transcription start sites during cerebellar development
title_fullStr Relatively frequent switching of transcription start sites during cerebellar development
title_full_unstemmed Relatively frequent switching of transcription start sites during cerebellar development
title_short Relatively frequent switching of transcription start sites during cerebellar development
title_sort relatively frequent switching of transcription start sites during cerebellar development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470264/
https://www.ncbi.nlm.nih.gov/pubmed/28610618
http://dx.doi.org/10.1186/s12864-017-3834-z
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