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Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms

Alternative splicing (AS) is a process in eukaryotic gene expression, in which the primary transcript of a multi-exon gene is spliced into two or more different mature transcripts, thereby increasing proteome diversity. AS is often regulated differentially between different tissues or developmental...

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Autores principales: Wang, Haifeng, You, Chenjiang, Chang, Fang, Wang, Yingxiang, Wang, Lei, Qi, Ji, Ma, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921568/
https://www.ncbi.nlm.nih.gov/pubmed/24575124
http://dx.doi.org/10.3389/fgene.2014.00025
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author Wang, Haifeng
You, Chenjiang
Chang, Fang
Wang, Yingxiang
Wang, Lei
Qi, Ji
Ma, Hong
author_facet Wang, Haifeng
You, Chenjiang
Chang, Fang
Wang, Yingxiang
Wang, Lei
Qi, Ji
Ma, Hong
author_sort Wang, Haifeng
collection PubMed
description Alternative splicing (AS) is a process in eukaryotic gene expression, in which the primary transcript of a multi-exon gene is spliced into two or more different mature transcripts, thereby increasing proteome diversity. AS is often regulated differentially between different tissues or developmental stages. Recent studies suggested that up to 60% of intron-containing genes in Arabidopsis thaliana undergo AS. Yet little is known about this complicated and important process during floral development. To investigate the preferential expression of different isoforms of individual alternatively spliced genes, we used high throughput RNA-Seq technology to explore the transcriptomes of three floral development stages of Arabidopsis thaliana and obtained information of various AS events. We identified approximately 24,000 genes that were expressed at one or more of these stages, and found that nearly 25% of multi-exon genes had two or more spliced variants. This is less frequent than the previously reported 40–60% for multiple organs and stages of A. thaliana, indicating that many genes expressed in floral development function with a single predominant isoform. On the other hand, 1716 isoforms were differentially expressed between the three stages, suggesting that AS might still play important roles in stage transition during floral development. Moreover, 337 novel transcribed regions were identified and most of them have a single exon. Taken together, our analyses provide a comprehensive survey of AS in floral development and facilitate further genomic and genetic studies.
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spelling pubmed-39215682014-02-26 Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms Wang, Haifeng You, Chenjiang Chang, Fang Wang, Yingxiang Wang, Lei Qi, Ji Ma, Hong Front Genet Genetics Alternative splicing (AS) is a process in eukaryotic gene expression, in which the primary transcript of a multi-exon gene is spliced into two or more different mature transcripts, thereby increasing proteome diversity. AS is often regulated differentially between different tissues or developmental stages. Recent studies suggested that up to 60% of intron-containing genes in Arabidopsis thaliana undergo AS. Yet little is known about this complicated and important process during floral development. To investigate the preferential expression of different isoforms of individual alternatively spliced genes, we used high throughput RNA-Seq technology to explore the transcriptomes of three floral development stages of Arabidopsis thaliana and obtained information of various AS events. We identified approximately 24,000 genes that were expressed at one or more of these stages, and found that nearly 25% of multi-exon genes had two or more spliced variants. This is less frequent than the previously reported 40–60% for multiple organs and stages of A. thaliana, indicating that many genes expressed in floral development function with a single predominant isoform. On the other hand, 1716 isoforms were differentially expressed between the three stages, suggesting that AS might still play important roles in stage transition during floral development. Moreover, 337 novel transcribed regions were identified and most of them have a single exon. Taken together, our analyses provide a comprehensive survey of AS in floral development and facilitate further genomic and genetic studies. Frontiers Media S.A. 2014-02-12 /pmc/articles/PMC3921568/ /pubmed/24575124 http://dx.doi.org/10.3389/fgene.2014.00025 Text en Copyright © 2014 Wang, You, Chang, Wang, Wang, Qi and Ma. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Wang, Haifeng
You, Chenjiang
Chang, Fang
Wang, Yingxiang
Wang, Lei
Qi, Ji
Ma, Hong
Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms
title Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms
title_full Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms
title_fullStr Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms
title_full_unstemmed Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms
title_short Alternative splicing during Arabidopsis flower development results in constitutive and stage-regulated isoforms
title_sort alternative splicing during arabidopsis flower development results in constitutive and stage-regulated isoforms
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921568/
https://www.ncbi.nlm.nih.gov/pubmed/24575124
http://dx.doi.org/10.3389/fgene.2014.00025
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