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用于盐胁迫下红麻比较转录谱分析的RNA测序

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

作者信息

Li Hui, Li Defang, Chen Anguo, Tang Huijuan, Li Jianjun, Huang Siqi

机构信息

Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, No. 348 West Xianjiahu Road, Changsha, 410205, China.

出版信息

J Plant Res. 2017 Mar;130(2):365-372. doi: 10.1007/s10265-016-0898-9. Epub 2016 Dec 20.

DOI:10.1007/s10265-016-0898-9
PMID:27999968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5318473/
Abstract

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.

摘要

红麻(Hibiscus cannabinus L.)是一种具有重要经济价值的全球天然纤维作物。由于对粮食作物的需求增加以及可耕地面积减少,红麻种植已越来越多地转向盐碱地。为了研究红麻耐盐性的分子机制,我们对红麻茎尖进行了Illumina高通量RNA测序,鉴定出71,318个单基因,并使用四个不同的蛋白质数据库对其进行了注释。总共在盐胁迫植物和对照植物之间鉴定出2,384个差异表达基因(DEG),其中1,702个转录本上调,683个转录本下调。鉴定出属于15个响应盐胁迫的转录因子家族的37个转录本。基因本体功能富集分析表明,编码抗氧化酶的基因上调。在盐胁迫条件下,这些DEG中氨基酸代谢和碳水化合物代谢途径高度富集。为了确认RNA-seq数据,我们随机选择了20个单基因,使用定量实时聚合酶链反应进行分析。我们的研究不仅提供了对红麻转录组资源的大规模评估,还为理解红麻盐胁迫响应机制提供了指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/e6e80a2f7f0e/10265_2016_898_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/5f0a19964879/10265_2016_898_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/a5aa6fe8dc67/10265_2016_898_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/a35e5809b055/10265_2016_898_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/e6e80a2f7f0e/10265_2016_898_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/5f0a19964879/10265_2016_898_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/a5aa6fe8dc67/10265_2016_898_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/a35e5809b055/10265_2016_898_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e4/5318473/e6e80a2f7f0e/10265_2016_898_Fig4_HTML.jpg

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