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Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots
BACKGROUND: Panax ginseng Meyer is a traditional medicinal plant famous for its strong therapeutic effects and serves as an important herbal medicine. To understand and manipulate genes involved in secondary metabolic pathways including ginsenosides, transcriptome profiling of P. ginseng is essentia...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213845/ https://www.ncbi.nlm.nih.gov/pubmed/25379008 http://dx.doi.org/10.1016/j.jgr.2014.05.008 |
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author | Jayakodi, Murukarthick Lee, Sang-Choon Park, Hyun-Seung Jang, Woojong Lee, Yun Sun Choi, Beom-Soon Nah, Gyoung Ju Kim, Do-Soon Natesan, Senthil Sun, Chao Yang, Tae-Jin |
author_facet | Jayakodi, Murukarthick Lee, Sang-Choon Park, Hyun-Seung Jang, Woojong Lee, Yun Sun Choi, Beom-Soon Nah, Gyoung Ju Kim, Do-Soon Natesan, Senthil Sun, Chao Yang, Tae-Jin |
author_sort | Jayakodi, Murukarthick |
collection | PubMed |
description | BACKGROUND: Panax ginseng Meyer is a traditional medicinal plant famous for its strong therapeutic effects and serves as an important herbal medicine. To understand and manipulate genes involved in secondary metabolic pathways including ginsenosides, transcriptome profiling of P. ginseng is essential. METHODS: RNA-seq analysis of adventitious roots of two P. ginseng cultivars, Chunpoong (CP) and Cheongsun (CS), was performed using the Illumina HiSeq platform. After transcripts were assembled, expression profiling was performed. RESULTS: Assemblies were generated from ∼85 million and ∼77 million high-quality reads from CP and CS cultivars, respectively. A total of 35,527 and 27,716 transcripts were obtained from the CP and CS assemblies, respectively. Annotation of the transcriptomes showed that approximately 90% of the transcripts had significant matches in public databases. We identified several candidate genes involved in ginsenoside biosynthesis. In addition, a large number of transcripts (17%) with different gene ontology designations were uniquely detected in adventitious roots compared to normal ginseng roots. CONCLUSION: This study will provide a comprehensive insight into the transcriptome of ginseng adventitious roots, and a way for successful transcriptome analysis and profiling of resource plants with less genomic information. The transcriptome profiling data generated in this study are available in our newly created adventitious root transcriptome database (http://im-crop.snu.ac.kr/transdb/index.php) for public use. |
format | Online Article Text |
id | pubmed-4213845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42138452014-11-06 Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots Jayakodi, Murukarthick Lee, Sang-Choon Park, Hyun-Seung Jang, Woojong Lee, Yun Sun Choi, Beom-Soon Nah, Gyoung Ju Kim, Do-Soon Natesan, Senthil Sun, Chao Yang, Tae-Jin J Ginseng Res Research Article BACKGROUND: Panax ginseng Meyer is a traditional medicinal plant famous for its strong therapeutic effects and serves as an important herbal medicine. To understand and manipulate genes involved in secondary metabolic pathways including ginsenosides, transcriptome profiling of P. ginseng is essential. METHODS: RNA-seq analysis of adventitious roots of two P. ginseng cultivars, Chunpoong (CP) and Cheongsun (CS), was performed using the Illumina HiSeq platform. After transcripts were assembled, expression profiling was performed. RESULTS: Assemblies were generated from ∼85 million and ∼77 million high-quality reads from CP and CS cultivars, respectively. A total of 35,527 and 27,716 transcripts were obtained from the CP and CS assemblies, respectively. Annotation of the transcriptomes showed that approximately 90% of the transcripts had significant matches in public databases. We identified several candidate genes involved in ginsenoside biosynthesis. In addition, a large number of transcripts (17%) with different gene ontology designations were uniquely detected in adventitious roots compared to normal ginseng roots. CONCLUSION: This study will provide a comprehensive insight into the transcriptome of ginseng adventitious roots, and a way for successful transcriptome analysis and profiling of resource plants with less genomic information. The transcriptome profiling data generated in this study are available in our newly created adventitious root transcriptome database (http://im-crop.snu.ac.kr/transdb/index.php) for public use. 2014-06-05 2014-10-15 /pmc/articles/PMC4213845/ /pubmed/25379008 http://dx.doi.org/10.1016/j.jgr.2014.05.008 Text en © 2014 The Korean Society of Ginseng. Published by Elsevier B.V. All rights reserved. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the CC-BY-NC License (http://creativecommons.org/licenses/by-nc/3.0). |
spellingShingle | Research Article Jayakodi, Murukarthick Lee, Sang-Choon Park, Hyun-Seung Jang, Woojong Lee, Yun Sun Choi, Beom-Soon Nah, Gyoung Ju Kim, Do-Soon Natesan, Senthil Sun, Chao Yang, Tae-Jin Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots |
title | Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots |
title_full | Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots |
title_fullStr | Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots |
title_full_unstemmed | Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots |
title_short | Transcriptome profiling and comparative analysis of Panax ginseng adventitious roots |
title_sort | transcriptome profiling and comparative analysis of panax ginseng adventitious roots |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213845/ https://www.ncbi.nlm.nih.gov/pubmed/25379008 http://dx.doi.org/10.1016/j.jgr.2014.05.008 |
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