4.6 Review Book Chapter

CRISPR/Cas9 in Genome Editing and Beyond

Journal

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85
Volume 85, Issue -, Pages 227-264

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-biochem-060815-014607

Keywords

dCas9; Cas9 structure; gene regulation; epigenetic regulation; genomic imaging; CRISPR applications

Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM008568] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [T32 GM008568] Funding Source: Medline

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The Cas9 protein (CRISPR-associated protein 9), derived from type II CRISPR (clustered regularly interspaced short palindromic repeats) bacterial immune systems, is emerging as a powerful tool for engineering the genome in diverse organisms. As an RNA-guided DNA endonuclease, Cas9 can be easily programmed to target new sites by altering its guide RNA sequence, and its development as a tool has made sequence-specific gene editing several magnitudes easier. The nuclease-deactivated form of Cas9 further provides a versatile RNA-guided DNA-targeting platform for regulating and imaging the genome, as well as for rewriting the epigenetic status, all in a sequence-specific manner. With all of these advances, we have just begun to explore the possible applications of Cas9 in biomedical research and therapeutics. In this review, we describe the current models of Cas9 function and the structural and biochemical studies that support it. We focus on the applications of Cas9 for genome editing, regulation, and imaging, discuss other possible applications and some technical considerations, and highlight the many advantages that CRISPR/Cas9 technology offers.

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