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Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.)
BACKGROUND: Alternative splicing (AS) represents a mechanism widely used by eukaryotes for the post-transcriptional regulation of genes. The detailed exploration of AS in peanut has not been documented. RESULTS: The strand-specific RNA-Seq technique was exploited to characterize the distribution of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032549/ https://www.ncbi.nlm.nih.gov/pubmed/29973157 http://dx.doi.org/10.1186/s12870-018-1339-9 |
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author | Ruan, Jian Guo, Feng Wang, Yingying Li, Xinguo Wan, Shubo Shan, Lei Peng, Zhenying |
author_facet | Ruan, Jian Guo, Feng Wang, Yingying Li, Xinguo Wan, Shubo Shan, Lei Peng, Zhenying |
author_sort | Ruan, Jian |
collection | PubMed |
description | BACKGROUND: Alternative splicing (AS) represents a mechanism widely used by eukaryotes for the post-transcriptional regulation of genes. The detailed exploration of AS in peanut has not been documented. RESULTS: The strand-specific RNA-Seq technique was exploited to characterize the distribution of AS in the four samples of peanut (FH1-seed1, FH1-seed2, FH1-root and FH1-leaf). AS was detected as affecting around 37.2% of the full set of multi-exon genes. Some of these genes experienced AS throughout the plant, while in the case of others, the effect was organ-specific. Overall, AS was more frequent in the seed than in either the root or leaf. The predominant form of AS was intron retention, and AS in transcription start site and transcription terminal site were commonly identified in all the four samples. It is interesting that in genes affected by AS, the majority experienced only a single type of event. Not all of the in silico predicted transcripts appeared to be translated, implying that these are either degraded or sequestered away from the translation machinery. With respect to genes involved in fatty acid metabolism, about 61.6% were shown to experience AS. CONCLUSION: Our report contributes significantly in AS analysis of peanut genes in general, and these results have not been mentioned before. The specific functions of different AS forms need further investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1339-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6032549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60325492018-07-11 Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) Ruan, Jian Guo, Feng Wang, Yingying Li, Xinguo Wan, Shubo Shan, Lei Peng, Zhenying BMC Plant Biol Research Article BACKGROUND: Alternative splicing (AS) represents a mechanism widely used by eukaryotes for the post-transcriptional regulation of genes. The detailed exploration of AS in peanut has not been documented. RESULTS: The strand-specific RNA-Seq technique was exploited to characterize the distribution of AS in the four samples of peanut (FH1-seed1, FH1-seed2, FH1-root and FH1-leaf). AS was detected as affecting around 37.2% of the full set of multi-exon genes. Some of these genes experienced AS throughout the plant, while in the case of others, the effect was organ-specific. Overall, AS was more frequent in the seed than in either the root or leaf. The predominant form of AS was intron retention, and AS in transcription start site and transcription terminal site were commonly identified in all the four samples. It is interesting that in genes affected by AS, the majority experienced only a single type of event. Not all of the in silico predicted transcripts appeared to be translated, implying that these are either degraded or sequestered away from the translation machinery. With respect to genes involved in fatty acid metabolism, about 61.6% were shown to experience AS. CONCLUSION: Our report contributes significantly in AS analysis of peanut genes in general, and these results have not been mentioned before. The specific functions of different AS forms need further investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1339-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-04 /pmc/articles/PMC6032549/ /pubmed/29973157 http://dx.doi.org/10.1186/s12870-018-1339-9 Text en © The Author(s). 2018 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 Ruan, Jian Guo, Feng Wang, Yingying Li, Xinguo Wan, Shubo Shan, Lei Peng, Zhenying Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) |
title | Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) |
title_full | Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) |
title_fullStr | Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) |
title_full_unstemmed | Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) |
title_short | Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.) |
title_sort | transcriptome analysis of alternative splicing in peanut (arachis hypogaea l.) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032549/ https://www.ncbi.nlm.nih.gov/pubmed/29973157 http://dx.doi.org/10.1186/s12870-018-1339-9 |
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