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有读书笔记有附件Microarray-based analysis of stress-regulated microRNAs in Arabidopsis thaliana

libingbing 添加于 2010-4-24 17:35 | 1708 次阅读 | 0 个评论
  •  作 者

    Liu H-H, Tian X, Li Y-J, Wu C-A, Zheng C-C
  •  摘 要

    High-salinity, drought, and low temperature are three common environmental stress factors that seriously influence plant growth and development worldwide. Recently, microRNAs (miRNAs) have emerged as a class of gene expression regulators that have also been linked to stress responses. However, the relationship between miRNA expression and stress responses is just beginning to be explored. Here, we identified 14 stress-inducible miRNAs using microarray data in which the effects of three abiotic stresses were surveyed in Arabidopsis thaliana. Among them, 10 high-salinity-, four drought-, and 10 cold-regulated miRNAs were detected, respectively. miR168, miR171, and miR396 responded to all of the stresses. Expression profiling by RT-PCR analysis showed great cross-talk among the high-salinity, drought, and cold stress signaling pathways. The existence of stress-related elements in miRNA promoter regions provided further evidence supporting our results. These findings extend the current view about miRNA as ubiquitous regulators under stress conditions.
  •  详细资料

    • 文献种类: Journal Article
    • 期刊名称: RNA
    • 期刊缩写: RNA
    • 期卷页: 2008  14 5 836-843
    • ISBN: 1355-8382
  • 学科领域 生物医药 » 生物学

  •  标 签

  • 相关链接 DOI URL 

  •  附 件

    PDF附件836.full.pdf 
  •  libingbing 的文献笔记  订阅

    【原创】本文通过miRNA 芯片获得相应盐,干旱,冷胁迫的miRNA(14个),基于它们靶基因地特点,分为三类,eight miRNAs—miR156, miR159, miR165, miR169, miR171, miR172,miR319, and miR396—which target transcription factors,再进一步响应胁迫;Thesecond category includes miR167, miR168, miR393, and
    miR394, which are related to direct response to stresses ,The last category includes miR397 and miR408, whose target genes are hydrolase and oxidoreductase coding genes, which respond to many
    stresses ,对于未检测到的miRNA,作者分析了原因,对于已经报道明显响应胁迫的miR389 and miR400 ,可能是treatment methods or technical differences between RNA gel blot and microarrayanalysis. 其他的,perhaps at low levels at this stage or their expression is limited to specific cell types or particular growth conditions;通过sqRTPCR来验证芯片结果,除了miR156h and miR167d,符合芯片结果;作者提取20个miRNA上游1000bp序列通过PLANTCARE分析了miRNA的启动子发现存在胁迫响应顺式作用元件,进一步证明了之前的14个miRNA可能参与逆境响应。对其他物种的miRNA的研究有参考价值!

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