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利用微阵列基因表达和计算方法鉴定秀丽隐杆线虫热休克反应中涉及的一种新型顺式调控元件。

Identification of a novel cis-regulatory element involved in the heat shock response in Caenorhabditis elegans using microarray gene expression and computational methods.

作者信息

GuhaThakurta Debraj, Palomar Lisanne, Stormo Gary D, Tedesco Pat, Johnson Thomas E, Walker David W, Lithgow Gordon, Kim Stuart, Link Christopher D

机构信息

Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63114, USA.

出版信息

Genome Res. 2002 May;12(5):701-12. doi: 10.1101/gr.228902.

Abstract

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.

摘要

我们在此报告在秀丽隐杆线虫中鉴定出一种先前未知的热休克(HS)基因转录调控元件。我们监测了秀丽隐杆线虫11917个基因的表达模式,以确定在热休克时上调的基因。在实验的几次不同重复中,观察到28个基因持续上调。我们使用计算DNA模式识别方法分析了这些基因的上游区域。通过这种方式鉴定出两个潜在的顺式调控基序。其中一个基序(TTCTAGAA)是热休克因子(HSF)的DNA结合基序,而另一个(GGGTGTC)在文献中此前未被报道。我们使用不同的统计测试和参数确定了这些基序对HS基因的重要性。对秀丽隐杆线虫和布氏秀丽隐杆线虫直系同源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。通过对由秀丽隐杆线虫hsp-16-2启动子驱动的绿色荧光蛋白(GFP)报告转基因进行体外诱变,测试了所鉴定的DNA位点在HS基因调控中的作用。对应于这两个基序的DNA位点在热休克时hsp-16-2基因的上调中均发挥重要作用。这是少数几个使用计算方法鉴定出的新型调控元件具有生物学活性的实例之一。各个位点对热休克时转录诱导的贡献是非累加性的,这表明这些位点之间存在相互作用和串扰,可能是通过与这些位点结合的转录因子(TFs)实现的。

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