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首页> 外文期刊>Sugar Tech >Identification of Differentially Expressed Genes in Sugarcane During Pathogenesis of Colletotrichum falcatum by Suppression Subtractive Hybridization (SSH)
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Identification of Differentially Expressed Genes in Sugarcane During Pathogenesis of Colletotrichum falcatum by Suppression Subtractive Hybridization (SSH)

机译:通过抑制消减杂交(SSH)鉴定在炭疽菌发病过程中甘蔗中差异表达的基因

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摘要

A suppression subtractive hybridization technique was used to identify differentially expressed genes in sugarcane in response to Colletotrichum falcatum, the fungal pathogen causing red rot in sugarcane. Messenger RNA (mRNA) samples collected from red rot resistant cv. Co 93009 at 6, 12, 24 and 48 h after pathogen challenge were pooled together and used as tester population. mRNA samples collected from red rot susceptible cv. CoC 671 at 6, 12, 24 and 48 h after pathogen challenge and control of samples of cv. Co 93009 and cv. CoC 671 were pooled together and used as the driver population. A forward subtraction enriched for differentially expressed ESTs in the resistant cultivar was carried out. At the end of subtraction, cloning and sequencing, 136 EST sequences were assembled into ten clusters/contigs. Based on TIGR homology search, the clusters were found to be involved in reactive oxygen species signaling, defense and the secretory pathway of plant innate immunity associated with hypersensitive response-mediated programmed cell death. Temporal gene expression pattern of the EST clusters by quantitative real time PCR revealed that, resistant cultivar had a higher level of gene expression than the susceptible cultivar in all the clusters till 48 h after pathogen inoculation. In conclusion, this study identified for the first time a set of differentially expressed EST clusters in red rot resistant sugarcane cultivar in response to C. falcatum infection.
机译:抑制消减杂交技术被用来识别甘蔗中的表达差异基因,该基因是对引起甘蔗红腐的真菌病原菌炭疽菌的反应。从抗红腐病的简历中收集的信使RNA(mRNA)样品。在病原体攻击后第6、12、24和48小时将Co 93009汇集在一起​​,并用作测试者种群。从易患红腐病的简历中收集的mRNA样本。在病原体攻击和cv样品对照后的6、12、24和48小时的CoC 671。公司93009和简历。将CoC 671汇集在一起​​并用作驱动程序种群。对在抗性品种中差异表达的EST进行了富集的正向扣除。在减法,克隆和测序结束时,将136个EST序列组装成十个簇/重叠群。基于TIGR同源性搜索,发现这些簇与活性氧介导的程序性细胞死亡相关的活性氧物种信号传导,防御和植物固有免疫的分泌途径。定量实时荧光定量PCR分析了EST簇的时间基因表达模式,表明在病原体接种后48小时,抗性品种的基因表达水平均高于易感品种。总之,本研究首次确定了抗腐烂念珠菌感染的抗红腐甘蔗品种中的一组差异表达的EST簇。

著录项

  • 来源
    《Sugar Tech》 |2016年第2期|176-183|共8页
  • 作者单位

    Indian Council Agr Res, Plant Pathol Sect, Div Crop Protect, Sugarcane Breeding Inst, Coimbatore 641007, Tamil Nadu, India;

    Indian Council Agr Res, Plant Pathol Sect, Div Crop Protect, Sugarcane Breeding Inst, Coimbatore 641007, Tamil Nadu, India;

    Indian Council Agr Res, Plant Pathol Sect, Div Crop Protect, Sugarcane Breeding Inst, Coimbatore 641007, Tamil Nadu, India;

    Indian Council Agr Res, Plant Pathol Sect, Div Crop Protect, Sugarcane Breeding Inst, Coimbatore 641007, Tamil Nadu, India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Sugarcane; Red rot; Host-pathogen interaction; Subtractive libraries; Real time PCR;

    机译:甘蔗;红腐病;宿主-病原体相互作用;消减文库;实时荧光定量PCR;

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