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      Editing the Epigenome: Technologies for Programmable Transcriptional Modulation and Epigenetic Regulation

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          Abstract

          Gene regulation is a highly complex and tightly controlled process that defines cell identity, health, and response to environmental signals. Technologies for precisely perturbing gene regulation are critical for improving our understanding of its coordination and for manipulating pathways for applications in biotechnology and medicine. Recently developed DNA-targeting platforms, including zinc finger proteins, TALEs, and CRISPR/Cas9, have enabled the recruitment of transcriptional modulators and epigenome-modifying factors to any genomic site. These technologies are generating novel insights into the function of epigenetic marks and the role of genome structure in gene expression. Additionally, custom transcriptional and epigenetic regulation is facilitating refined control over cell function and decision-making. The unique properties of the CRISPR/Cas9 system have also created new opportunities for multiplexing targets and manipulating complex gene expression patterns, as well as high-throughput genetic screens. This review summarizes recent technology developments in this area and their applications to modern biomedical challenges. We also discuss remaining limitations and necessary future directions for this field.

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          Author and article information

          Journal
          101215604
          32338
          Nat Methods
          Nat. Methods
          Nature methods
          1548-7091
          1548-7105
          27 May 2016
          February 2016
          01 February 2017
          : 13
          : 2
          : 127-137
          Affiliations
          [1 ]Department of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America, 27708
          [2 ]Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America, 27708
          [3 ]Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, United States of America, 27710
          Author notes
          Address for correspondence: Charles A. Gersbach, Ph.D., Department of Biomedical Engineering, Room 1427, FCIEMAS, 101 Science Drive, Box 90281, Duke University, Durham, NC 27708-0281, 919-613-2147, charles.gersbach@ 123456duke.edu
          Article
          PMC4922638 PMC4922638 4922638 nihpa781185
          10.1038/nmeth.3733
          4922638
          26820547
          6fc05a07-8d52-4d47-a164-3008a16fd148
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