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High-throughput methods of regulatory element discovery

机译:高通量调控元素发现方法

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摘要

With the number of organisms whose genomes have been sequenced, a vast amount of information concerning the genetic structure of an organism's genome has been collected. However, effective experiment means to study how this information is accessed have only recently been developed. In this review, three basic methods for identifying regions of protein-DNA interaction will be introduced. The first two, chromatin immunoprecipitation (ChIP)-chip and ChIP-PET (for paired-end ditag), rely on the enrichment provided by chromosomal immunoprecipitation to interrogate the genomic sequence for the interaction sites of a protein of interest. In contrast, protein microarrays allow the identification of DNA binding protein that interacts with a DNA sequence of interest. These complementary methods of exploring protein-DNA interactions will increase our fundamental knowledge of how the information contained within the genome sequence is accessed and processed.
机译:随着基因组已被测序的生物数量的增加,已经收集了有关生物基因组遗传结构的大量信息。但是,最近才开发出有效的实验手段来研究如何访问此信息。在这篇综述中,将介绍识别蛋白质-DNA相互作用区域的三种基本方法。前两个是染色质免疫沉淀(ChIP)芯片和ChIP-PET(用于双末端双标签),依靠染色体免疫沉淀提供的富集来询问目的蛋白质相互作用位点的基因组序列。相反,蛋白质微阵列允许鉴定与目的DNA序列相互作用的DNA结合蛋白。这些探索蛋白质-DNA相互作用的互补方法将增加我们对如何访问和处理基因组序列中所含信息的基础知识。

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