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SWI/SNF complexes and facilitation of TATA binding protein:nucleosome interactions.SWI/SNF复合物与TATA结合蛋白:核小体相互作用的促进作用
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DNA structure in human RNA polymerase II promoters.人类RNA聚合酶II启动子中的DNA结构。
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Architectural specificity in chromatin structure at the TATA box in vivo: nucleosome displacement upon beta-phaseolin gene activation.体内TATA框处染色质结构的建筑学特异性:菜豆β-球蛋白基因激活时核小体的移位
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New DNA sequence rules for high affinity binding to histone octamer and sequence-directed nucleosome positioning.与组蛋白八聚体高亲和力结合及序列导向核小体定位的新DNA序列规则。
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The Eukaryotic Promoter Database EPD.真核生物启动子数据库EPD。
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Nucleosome positioning and transcription-associated chromatin alterations on the human estrogen-responsive pS2 promoter.人类雌激素反应性pS2启动子上的核小体定位及与转录相关的染色质改变
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转录因子位点在启动子区域的周期性分布及其与染色质结构的关联

Periodical distribution of transcription factor sites in promoter regions and connection with chromatin structure.

作者信息

Ioshikhes I, Trifonov E N, Zhang M Q

机构信息

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.

出版信息

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2891-5. doi: 10.1073/pnas.96.6.2891.

DOI:10.1073/pnas.96.6.2891
PMID:10077607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC15865/
Abstract

Nucleosomes regulate transcriptional initiation when positioned in the promoter area. This may require the transcription factor (TF) sites to be correlated with the nucleosome positions and phased on the nucleosome surface. If this is the case, one would expect a periodical distribution of TF sites in the vicinity of promoters, with the nucleosomal period of 10.1-10.5 bp. We examined the distributions of putative binding sites of 323 different TFs along 1, 057 sequences of the Eukaryotic Promoter Database (release 50) [Cavin Perier, R., Junier, T. & Bucher, P. (1998) Nucleic Acids Res. 26, 353-357] and of 218 TFs on 673 sequences of the Lead Exon Database of human promoter sequences. We obtained a statistically significant overrepresentation of TF sites distributed with the main period of 10.1-10.5 bp in the region -50 to +120 around the transcription start site and in few locations nearby. Correlation of the positioning of the TF sites with the nucleosomes is further reinforced by sequence-directed mapping of the nucleosomes, a method previously developed.

摘要

当核小体位于启动子区域时,它们会调节转录起始。这可能需要转录因子(TF)位点与核小体位置相关,并在核小体表面呈相位分布。如果是这种情况,人们会预期在启动子附近TF位点呈周期性分布,核小体周期为10.1 - 10.5碱基对。我们研究了323种不同TF的假定结合位点沿真核生物启动子数据库(第50版)[Cavin Perier, R., Junier, T. & Bucher, P. (1998) Nucleic Acids Res. 26, 353 - 357]的1057个序列以及218种TF在人类启动子序列的前导外显子数据库的673个序列上的分布。我们发现在转录起始位点周围-50至+120区域以及附近的少数位置,TF位点以10.1 - 10.5碱基对的主要周期分布,具有统计学上显著的过度代表性。先前开发的一种方法——核小体的序列定向映射,进一步加强了TF位点定位与核小体之间的相关性。