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CRISPR technologies for genome, epigenome and transcriptome editing.
Villiger, Lukas; Joung, Julia; Koblan, Luke; Weissman, Jonathan; Abudayyeh, Omar O; Gootenberg, Jonathan S.
Affiliation
  • Villiger L; McGovern Institute for Brain Research, Massachusetts Institute of Technology Cambridge, Cambridge, MA, USA.
  • Joung J; Whitehead Institute for Biomedical Research, Cambridge, MA, USA.
  • Koblan L; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Weissman J; Whitehead Institute for Biomedical Research, Cambridge, MA, USA.
  • Abudayyeh OO; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Gootenberg JS; Whitehead Institute for Biomedical Research, Cambridge, MA, USA.
Nat Rev Mol Cell Biol ; 25(6): 464-487, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38308006
ABSTRACT
Our ability to edit genomes lags behind our capacity to sequence them, but the growing understanding of CRISPR biology and its application to genome, epigenome and transcriptome engineering is narrowing this gap. In this Review, we discuss recent developments of various CRISPR-based systems that can transiently or permanently modify the genome and the transcriptome. The discovery of further CRISPR enzymes and systems through functional metagenomics has meaningfully broadened the applicability of CRISPR-based editing. Engineered Cas variants offer diverse capabilities such as base editing, prime editing, gene insertion and gene regulation, thereby providing a panoply of tools for the scientific community. We highlight the strengths and weaknesses of current CRISPR tools, considering their efficiency, precision, specificity, reliance on cellular DNA repair mechanisms and their applications in both fundamental biology and therapeutics. Finally, we discuss ongoing clinical trials that illustrate the potential impact of CRISPR systems on human health.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcriptome / CRISPR-Cas Systems / Gene Editing / Epigenome Limits: Animals / Humans Language: En Journal: Nat Rev Mol Cell Biol Journal subject: BIOLOGIA MOLECULAR Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcriptome / CRISPR-Cas Systems / Gene Editing / Epigenome Limits: Animals / Humans Language: En Journal: Nat Rev Mol Cell Biol Journal subject: BIOLOGIA MOLECULAR Year: 2024 Type: Article Affiliation country: United States