首页> 美国卫生研究院文献>Genome Research >Identification of a Novel cis-Regulatory Element Involved in the Heat Shock Response in Caenorhabditis elegans Using Microarray Gene Expression and Computational Methods
【2h】

Identification of a Novel cis-Regulatory Element Involved in the Heat Shock Response in Caenorhabditis elegans Using Microarray Gene Expression and Computational Methods

机译:使用芯片基因表达和计算方法鉴定一种新型的顺式调控元件参与秀丽隐杆线虫的热休克反应。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We report here the identification of a previously unknown transcription regulatory element for heat shock (HS) genes in Caenorhabditis elegans. We monitored the expression pattern of 11,917 genes from C. elegans to determine the genes that were up-regulated on HS. Twenty eight genes were observed to be consistently up-regulated in several different repetitions of the experiments. We analyzed the upstream regions of these genes using computational DNA pattern recognition methods. Two potential cis-regulatory motifs were identified in this way. One of these motifs (TTCTAGAA) was the DNA binding motif for the heat shock factor (HSF), whereas the other (GGGTGTC) was previously unreported in the literature. We determined the significance of these motifs for the HS genes using different statistical tests and parameters. Comparative sequence analysis of orthologous HS genes from C. elegans and Caenorhabditis briggsae indicated that the identified DNA regulatory motifs are conserved across related species. The role of the identified DNA sites in regulation of HS genes was tested by in vitro mutagenesis of a green fluorescent protein (GFP) reporter transgene driven by the C. elegans hsp-16–2 promoter. DNA sites corresponding to both motifs are shown to play a significant role in up-regulation of the hsp-16–2 gene on HS. This is one of the rare instances in which a novel regulatory element, identified using computational methods, is shown to be biologically active. The contributions of individual sites toward induction of transcription on HS are nonadditive, which indicates interaction and cross-talk between the sites, possibly through the transcription factors (TFs) binding to these sites.[The following individuals kindly provided reagents, samples, or unpublished information as indicated in the paper: L. Hillier.]
机译:我们在这里报告的秀丽隐杆线虫热休克(HS)基因的一个以前未知的转录调控元件的鉴定。我们监测了秀丽隐杆线虫的11,917个基因的表达模式,以确定在HS上调的基因。在几个不同的实验重复中,观察到28个基因被一致地上调。我们使用计算的DNA模式识别方法分析了这些基因的上游区域。以这种方式鉴定了两个潜在的顺式调控基序。这些基序之一(TTCTAGAA)是热激因子(HSF)的DNA结合基序,而另一个(GGGTGTC)在文献中未见报道。我们使用不同的统计测试和参数确定了这些基序对于HS基因的重要性。来自秀丽隐杆线虫和秀丽隐杆线虫的直系同源HS基因的比较序列分析表明,所鉴定的DNA调控基序在相关物种中是保守的。通过体外诱变由秀丽隐杆线虫hsp-16-2启动子驱动的绿色荧光蛋白(GFP)报告基因转基因,测试了已鉴定的DNA位点在HS基因调控中的作用。已显示与两个基序对应的DNA位点在HS上hsp-16-2基因的上调中起重要作用。这是罕见的情况之一,其中使用计算方法鉴定的新型调节元件被证明具有生物活性。单个位点对HS上的转录诱导的贡献是非累加的,这表明这些位点之间的相互作用和串扰可能是通过与这些位点结合的转录因子(TF)引起的。[以下人员请提供试剂,样品或未公开文件中指出的信息:L。Hillier。]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号