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RNA-seq for comparative transcript profiling of kenaf under salinity stress

Kenaf (Hibiscus cannabinus L.) is an economically important global natural fiber crop. As a consequence of the increased demand for food crops and the reduction of available arable land, kenaf cultivation has increasingly shifted to saline and alkaline land. To investigate the molecular mechanism of...

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Autores principales: Li, Hui, Li, Defang, Chen, Anguo, Tang, Huijuan, Li, Jianjun, Huang, Siqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318473/
https://www.ncbi.nlm.nih.gov/pubmed/27999968
http://dx.doi.org/10.1007/s10265-016-0898-9
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author Li, Hui
Li, Defang
Chen, Anguo
Tang, Huijuan
Li, Jianjun
Huang, Siqi
author_facet Li, Hui
Li, Defang
Chen, Anguo
Tang, Huijuan
Li, Jianjun
Huang, Siqi
author_sort Li, Hui
collection PubMed
description Kenaf (Hibiscus cannabinus L.) is an economically important global natural fiber crop. As a consequence of the increased demand for food crops and the reduction of available arable land, kenaf cultivation has increasingly shifted to saline and alkaline land. To investigate the molecular mechanism of salinity tolerance in kenaf, we performed Illumina high-throughput RNA sequencing on shoot tips of kenaf and identified 71,318 unigenes, which were annotated using four different protein databases. In total, 2,384 differentially expressed genes (DEGs) were identified between the salt-stressed and the control plants, 1,702 of these transcripts were up-regulated and 683 transcripts were down-regulated. Thirty-seven transcripts belonging to 15 transcription-factor families that respond to salt stress were identified. Gene ontology function enrichment analysis revealed that the genes encoding antioxidant enzymes were up-regulated. The amino acid metabolism and carbohydrate metabolism pathways were highly enriched among these DEGs under salt stress conditions. In order to confirm the RNA-seq data, we randomly selected 20 unigenes for analysis using a quntitative real-time polymerase chain reaction. Our study not only provided the large-scale assessment of transcriptome resources of kenaf but also guidelines for understanding the mechanism underlying salt stress responses in kenaf. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10265-016-0898-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-53184732017-03-06 RNA-seq for comparative transcript profiling of kenaf under salinity stress Li, Hui Li, Defang Chen, Anguo Tang, Huijuan Li, Jianjun Huang, Siqi J Plant Res Regular Paper Kenaf (Hibiscus cannabinus L.) is an economically important global natural fiber crop. As a consequence of the increased demand for food crops and the reduction of available arable land, kenaf cultivation has increasingly shifted to saline and alkaline land. To investigate the molecular mechanism of salinity tolerance in kenaf, we performed Illumina high-throughput RNA sequencing on shoot tips of kenaf and identified 71,318 unigenes, which were annotated using four different protein databases. In total, 2,384 differentially expressed genes (DEGs) were identified between the salt-stressed and the control plants, 1,702 of these transcripts were up-regulated and 683 transcripts were down-regulated. Thirty-seven transcripts belonging to 15 transcription-factor families that respond to salt stress were identified. Gene ontology function enrichment analysis revealed that the genes encoding antioxidant enzymes were up-regulated. The amino acid metabolism and carbohydrate metabolism pathways were highly enriched among these DEGs under salt stress conditions. In order to confirm the RNA-seq data, we randomly selected 20 unigenes for analysis using a quntitative real-time polymerase chain reaction. Our study not only provided the large-scale assessment of transcriptome resources of kenaf but also guidelines for understanding the mechanism underlying salt stress responses in kenaf. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10265-016-0898-9) contains supplementary material, which is available to authorized users. Springer Japan 2016-12-20 2017 /pmc/articles/PMC5318473/ /pubmed/27999968 http://dx.doi.org/10.1007/s10265-016-0898-9 Text en © The Author(s) 2016 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.
spellingShingle Regular Paper
Li, Hui
Li, Defang
Chen, Anguo
Tang, Huijuan
Li, Jianjun
Huang, Siqi
RNA-seq for comparative transcript profiling of kenaf under salinity stress
title RNA-seq for comparative transcript profiling of kenaf under salinity stress
title_full RNA-seq for comparative transcript profiling of kenaf under salinity stress
title_fullStr RNA-seq for comparative transcript profiling of kenaf under salinity stress
title_full_unstemmed RNA-seq for comparative transcript profiling of kenaf under salinity stress
title_short RNA-seq for comparative transcript profiling of kenaf under salinity stress
title_sort rna-seq for comparative transcript profiling of kenaf under salinity stress
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318473/
https://www.ncbi.nlm.nih.gov/pubmed/27999968
http://dx.doi.org/10.1007/s10265-016-0898-9
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