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CRISPR beyond: harnessing compact RNA-guided endonucleases for enhanced genome editing.
Wang, Feizuo; Ma, Shengsheng; Zhang, Senfeng; Ji, Quanquan; Hu, Chunyi.
Afiliação
  • Wang F; Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore.
  • Ma S; Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore.
  • Zhang S; Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore.
  • Ji Q; Cancer Science Institute of Singapore, National University of Singapore, Singapore, 117597, Singapore. jqq@nus.edu.sg.
  • Hu C; Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore. hu_dbs@nus.edu.sg.
Sci China Life Sci ; 2024 Jul 12.
Article em En | MEDLINE | ID: mdl-39012436
ABSTRACT
The CRISPR-Cas system, an adaptive immunity system in prokaryotes designed to combat phages and foreign nucleic acids, has evolved into a groundbreaking technology enabling gene knockout, large-scale gene insertion, base editing, and nucleic acid detection. Despite its transformative impact, the conventional CRISPR-Cas effectors face a significant hurdle-their size poses challenges in effective delivery into organisms and cells. Recognizing this limitation, the imperative arises for the development of compact and miniature gene editors to propel advancements in gene-editing-related therapies. Two strategies were accepted to develop compact genome editors harnessing OMEGA (Obligate Mobile Element-guided Activity) systems, or engineering the existing CRISPR-Cas system. In this review, we focus on the advances in miniature genome editors based on both of these strategies. The objective is to unveil unprecedented opportunities in genome editing by embracing smaller, yet highly efficient genome editors, promising a future characterized by enhanced precision and adaptability in the genetic interventions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article