High throughput technologies for the functional discovery of mammalian enhancers: New approaches for understanding transcriptional regulatory network dynamics

被引:19
作者
Dailey, Lisa [1 ]
机构
[1] NYU, Sch Med, Dept Microbiol, Kimmel Ctr Stem Cell Biol, New York, NY 10016 USA
关键词
Transcription; Chromatin; Enhancers; Transcription factors; Development; Genome; RNA-POLYMERASE-II; HYPERSENSITIVE SITES; EMBRYONAL CARCINOMA; GENE-EXPRESSION; CHROMATIN; BINDING; DNA; ELEMENTS; SIGNATURES; PROMOTERS;
D O I
10.1016/j.ygeno.2015.06.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Completion of the human and mouse genomes has inspired new initiatives to obtain a global understanding of the functional regulatory networks governing gene expression. Enhancers are primary regulatory DNA elements determining precise spatio- and temporal gene expression patterns, but the observation that they can function at any distance from the gene(s) they regulate has made their genome-wide characterization challenging. Since traditional, single reporter approaches would be unable to accomplish this enormous task, high throughput technologies for mapping chromatin features associated with enhancers have emerged as an effective surrogate for enhancer discovery. However, the last few years have witnessed the development of several new innovative approaches that can effectively screen for and discover enhancers based on their functional activation of transcription using massively parallel reporter systems. In addition to their application for genome annotation, these new high throughput functional approaches open new and exciting avenues for modeling gene regulatory networks. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:151 / 158
页数:8
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