Transcriptome profiling of the UV-B stress response in the desert shrub Lycium ruthenicum
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  • 作者:Haikui Chen (1) (2)
    Yang Feng (2)
    Lina Wang (2)
    Takahiro Yonezawa (2)
    M. James C. Crabbe (3) (4)
    Xiu Zhang (1)
    Yang Zhong (2) (5)

    1. Department of Life Science
    ; Beifang University of Nationalities ; Yinchuan ; 750021 ; China
    2. School of Life Sciences
    ; Fudan University ; Shanghai ; 200433 ; China
    3. Department of Zoology
    ; Tinbergen Building ; University of Oxford ; South Parks Road ; Oxford ; OX1 3PS ; UK
    4. Institute of Biomedical and Environmental Science & Technology
    ; Faculty of Creative Arts ; Technologies and Science ; University of Bedfordshire ; Park Square ; Luton ; LU1 3JU ; UK
    5. Institute of Biodiversity Science and Geobiology
    ; Tibet University ; Lhasa ; 850000 ; China
  • 关键词:Ultraviolet ; Lycium ruthenicum ; Stress response ; Transcriptome ; RNA ; seq
  • 刊名:Molecular Biology Reports
  • 出版年:2015
  • 出版时间:March 2015
  • 年:2015
  • 卷:42
  • 期:3
  • 页码:639-649
  • 全文大小:856 KB
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  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Animal Anatomy, Morphology and Histology
    Animal Biochemistry
  • 出版者:Springer Netherlands
  • ISSN:1573-4978
文摘
Ultraviolet-B (UV-B) is a natural component of the solar radiation. Due to its high energy, low dosages of UV-B can bring huge potential damage effect to organisms. Despite much research that has analyzed the gene expression changes of plants that under UV-B radiation, the transcriptome response of Lycium ruthenicum under the UV-B induction is still un-available. The aim of our study was to identify UV-B responsive genes and gain an insight into the underlying genetic basis of the pathobiology of UV-B related damage. We collected leaf samples from L. ruthenicum with and without UV-B exposure, and then performed a transcriptome profiling to comprehensively investigate their expression signatures. By employing the high throughput RNA-sequencing analysis of samples with and without UV-B exposure, we identified 1,913 up-regulated and 536 down-regulated genes at least by twofold changes. The activity of antioxidant enzyme related genes, including the superoxide dismutase, was decreased, genes related to the synthesis of secondary metabolites and defense responses, such as cinnamyl alcohol dehydrogenase, chalcone-flavanone isomerase and dihydroflavonol reductase were also downregulated. The expression patterns of 14 randomly selected genes resulted from quantitative real-time PCR were basically consistent with their transcript abundance changes identified by RNA-sequencing. We found that several biological pathways related to biotic and abiotic stresses, including cell defense, photosynthesis processes, energy metabolism, were involved in the process of UV-B stress response. A genome-wide screening of gene deregulation under UV-B induction would provide an insight into the understanding of the molecular bases and pathogenesis of UV-B responses.

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