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在体作图揭示拟南芥支架/基质附着区与不利于核小体的聚(dA:dT)序列的关联。

In vivo mapping of arabidopsis scaffold/matrix attachment regions reveals link to nucleosome-disfavoring poly(dA:dT) tracts.

机构信息

Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, North Carolina 27695.

出版信息

Plant Cell. 2014 Jan;26(1):102-20. doi: 10.1105/tpc.113.121194. Epub 2014 Jan 31.

Abstract

Scaffold or matrix attachment regions (S/MARs) are found in all eukaryotes. The pattern of distribution and genomic context of S/MARs is thought to be important for processes such as chromatin organization and modulation of gene expression. Despite the importance of such processes, much is unknown about the large-scale distribution and sequence content of S/MARs in vivo. Here, we report the use of tiling microarrays to map 1358 S/MARs on Arabidopsis thaliana chromosome 4 (chr4). S/MARs occur throughout chr4, spaced much more closely than in the large plant and animal genomes that have been studied to date. Arabidopsis S/MARs can be divided into five clusters based on their association with other genomic features, suggesting a diversity of functions. While some Arabidopsis S/MARs may define structural domains, most occur near the transcription start sites of genes. Genes associated with these S/MARs have an increased probability of expression, which is particularly pronounced in the case of transcription factor genes. Analysis of sequence motifs and 6-mer enrichment patterns show that S/MARs are preferentially enriched in poly(dA:dT) tracts, sequences that resist nucleosome formation, and the majority of S/MARs contain at least one nucleosome-depleted region. This global view of S/MARs provides a framework to begin evaluating genome-scale models for S/MAR function.

摘要

支架或基质附着区 (S/MARs) 存在于所有真核生物中。S/MARs 的分布模式和基因组环境被认为对染色质组织和基因表达调控等过程很重要。尽管这些过程很重要,但关于 S/MARs 在体内的大规模分布和序列内容知之甚少。在这里,我们报告了使用平铺微阵列在拟南芥第 4 号染色体 (chr4) 上绘制 1358 个 S/MAR 的情况。S/MAR 遍布 chr4,与迄今为止研究过的大型植物和动物基因组相比,它们的间隔更近。根据与其他基因组特征的关联,拟南芥 S/MAR 可以分为五个簇,这表明它们具有多种功能。虽然一些拟南芥 S/MAR 可能定义了结构域,但大多数位于基因的转录起始位点附近。与这些 S/MAR 相关的基因表达的可能性增加,这在转录因子基因的情况下尤为明显。序列基序和 6- 碱基富集模式的分析表明,S/MAR 优先富集在多(dA:dT)片段中,这些序列抵抗核小体形成,并且大多数 S/MAR 至少包含一个核小体缺失区域。这种对 S/MARs 的全局观察为开始评估 S/MAR 功能的全基因组模型提供了框架。

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