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Identifying and Characterizing Regulatory Sequences in the Human Genome with Chromatin Accessibility Assays

机译:用染色质可及性测定鉴定和表征人类基因组中的调控序列

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摘要

After finishing a human genome reference sequence in 2002, the genomics community has turned to the task of interpreting it. A primary focus is to identify and characterize not only protein-coding genes, but all functional elements in the genome. The effort includes both individual investigators and large-scale projects like the Encyclopedia of DNA Elements (ENCODE) project. As part of the ENCODE project, several groups have identified millions of regulatory elements in hundreds of human cell-types using DNase-seq and FAIRE-seq experiments that detect regions of nucleosome-free open chromatin. ChIP-seq experiments have also been used to discover transcription factor binding sites and map histone modifications. Nearly all identified elements are found in non-coding DNA, hypothesizing a function for previously unannotated sequence. In this review, we provide an overview of the ENCODE effort to define regulatory elements, summarize the main results, and discuss implications of the millions of regulatory elements distributed throughout the genome.
机译:在2002年完成人类基因组参考序列后,基因组学界开始着手解释它。主要重点是不仅要识别和表征蛋白质编码基因,而且要鉴定和表征基因组中的所有功能元件。这项工作既包括个人研究人员,也包括大型项目,例如DNA元素百科全书(ENCODE)项目。作为ENCODE项目的一部分,使用DNase-seq和FAIRE-seq实验检测了无核小体的开放染色质区域,数个小组已经鉴定了数百种人类细胞类型中的数百万个调控元件。 ChIP-seq实验也已用于发现转录因子结合位点并绘制组蛋白修饰图。几乎所有已识别的元素都存在于非编码DNA中,从而推测了先前未注释序列的功能。在这篇综述中,我们概述了ENCODE定义调控元件,总结主要结果并讨论了分布在整个基因组中的数百万个调控元件的影响。

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