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拟南芥染色质中DNase I超敏感位点的定位与表征

Mapping and characterization of DNase I hypersensitive sites in Arabidopsis chromatin.

作者信息

Kodama Yuichi, Nagaya Shingo, Shinmyo Atsuhiko, Kato Ko

机构信息

Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Nara, 630-0192, Japan.

出版信息

Plant Cell Physiol. 2007 Mar;48(3):459-70. doi: 10.1093/pcp/pcm017. Epub 2007 Feb 5.

DOI:10.1093/pcp/pcm017
PMID:17283013
Abstract

Recent genome-wide analyses of yeast and human chromatin revealed the widespread prevalence of DNase I hypersensitive sites (DNase I HSs) at gene regulatory regions with possible roles in eukaryotic gene regulation. The presence of DNase I HSs in plants has been described for only a few genes, and we analyzed the chromatin structure of an 80 kb genomic region containing 30 variably expressed genes by DNase I sensitivity assay at 500 bp resolution in Arabidopsis. Distinct DNase I HSs were found at the 5' and/or 3' ends of most genes irrespective of their expression levels. Further analysis of well-characterized genes showed that the DNase I HSs occurred near cis-regulatory elements in the promoters of these genes. Upon transcriptional activation of a heat-inducible gene, the DNase I HS was extended into the vicinity of a cis-element and adjacent TATA element in the promoter. Concomitant with this change in DNase I HS, histones were acetylated, removed from the promoter, and a transcription activator bound to this cis-element. These results suggest that the DNase I HSs participate in the transcriptional regulation of Arabidopsis genes by enhancing the access of chromatin remodeling factors and/or transcription factors to their target sites as seen in yeast and human chromatin.

摘要

最近对酵母和人类染色质进行的全基因组分析表明,脱氧核糖核酸酶I超敏位点(DNase I HSs)在基因调控区域广泛存在,可能在真核基因调控中发挥作用。植物中仅对少数基因描述了DNase I HSs的存在,我们通过拟南芥中分辨率为500 bp的DNase I敏感性分析,分析了一个包含30个表达水平各异基因的80 kb基因组区域的染色质结构。无论基因表达水平如何,在大多数基因的5'和/或3'端都发现了明显的DNase I HSs。对特征明确的基因进行的进一步分析表明,DNase I HSs出现在这些基因启动子中的顺式调控元件附近。在一个热诱导基因转录激活后,DNase I HS延伸到启动子中一个顺式元件和相邻TATA元件附近。伴随着DNase I HS的这种变化,组蛋白被乙酰化,从启动子上移除,并且一个转录激活因子与这个顺式元件结合。这些结果表明,DNase I HSs通过增强染色质重塑因子和/或转录因子对其靶位点的可及性,参与拟南芥基因的转录调控,这与酵母和人类染色质中的情况类似。

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