Functional interrogation of non-coding DNA through CRISPR genome editing

Methods. 2017 May 15:121-122:118-129. doi: 10.1016/j.ymeth.2017.03.008. Epub 2017 Mar 10.

Abstract

Methodologies to interrogate non-coding regions have lagged behind coding regions despite comprising the vast majority of the genome. However, the rapid evolution of clustered regularly interspaced short palindromic repeats (CRISPR)-based genome editing has provided a multitude of novel techniques for laboratory investigation including significant contributions to the toolbox for studying non-coding DNA. CRISPR-mediated loss-of-function strategies rely on direct disruption of the underlying sequence or repression of transcription without modifying the targeted DNA sequence. CRISPR-mediated gain-of-function approaches similarly benefit from methods to alter the targeted sequence through integration of customized sequence into the genome as well as methods to activate transcription. Here we review CRISPR-based loss- and gain-of-function techniques for the interrogation of non-coding DNA.

Publication types

  • Review

MeSH terms

  • Animals
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • CRISPR-Associated Protein 9
  • CRISPR-Cas Systems*
  • Clustered Regularly Interspaced Short Palindromic Repeats*
  • DNA, Intergenic / genetics*
  • DNA, Intergenic / metabolism
  • Endonucleases / genetics*
  • Endonucleases / metabolism
  • Gain of Function Mutation
  • Gene Editing / methods*
  • Genome
  • Humans
  • Loss of Function Mutation
  • Plasmids / chemistry
  • Plasmids / metabolism
  • RNA, Guide, CRISPR-Cas Systems / genetics*
  • RNA, Guide, CRISPR-Cas Systems / metabolism
  • Sequence Analysis, DNA

Substances

  • Bacterial Proteins
  • DNA, Intergenic
  • RNA, Guide, CRISPR-Cas Systems
  • CRISPR-Associated Protein 9
  • Cas9 endonuclease Streptococcus pyogenes
  • Endonucleases