Cas12a Base Editors Induce Efficient and Specific Editing with Low DNA Damage Response

Cell Rep. 2020 Jun 2;31(9):107723. doi: 10.1016/j.celrep.2020.107723.

Abstract

The advent of base editors (BEs) holds great potential for correcting pathogenic-related point mutations to treat relevant diseases. However, Cas9 nickase (nCas9)-derived BEs lead to DNA double-strand breaks, which can trigger unwanted DNA damage response (DDR). Here, we show that the original version of catalytically dead Cas12a (dCas12a)-conjugated BEs induce a basal level of DNA breaks and minimally activate DDR proteins, including H2AX, ATM, ATR, and p53. By fusing dCas12a with engineered human apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A (APOBEC3A), we further develop the BEACON (base editing induced by human APOBEC3A and Cas12a without DNA break) system to achieve enhanced deamination efficiency and editing specificity. Efficient C-to-T editing is achieved by BEACON in mammalian cells at levels comparable to AncBE4max, with only low levels of DDR and minimal RNA off-target mutations. Importantly, BEACON induces in vivo base editing in mouse embryos, and targeted C-to-T conversions are detected in F0 mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 17-Hydroxysteroid Dehydrogenases / genetics
  • Animals
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • CRISPR-Associated Proteins / genetics
  • CRISPR-Associated Proteins / metabolism*
  • Cytidine / metabolism
  • Cytidine Deaminase / genetics
  • Cytidine Deaminase / metabolism
  • DNA Damage*
  • DNA Replication
  • Deamination
  • Endodeoxyribonucleases / genetics
  • Endodeoxyribonucleases / metabolism*
  • Female
  • Gene Editing / methods*
  • HEK293 Cells
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Phosphorylation
  • Proteins / genetics
  • Proteins / metabolism
  • Thymidine / metabolism
  • Tumor Suppressor Protein p53 / metabolism
  • Ubiquitins / metabolism

Substances

  • Bacterial Proteins
  • CRISPR-Associated Proteins
  • Proteins
  • Tumor Suppressor Protein p53
  • UBL5 protein, human
  • Ubiquitins
  • Cytidine
  • 17-Hydroxysteroid Dehydrogenases
  • 17beta-hydroxysteroid dehydrogenase type 3
  • Ataxia Telangiectasia Mutated Proteins
  • Cas12a protein
  • Endodeoxyribonucleases
  • APOBEC3A protein, human
  • Cytidine Deaminase
  • Thymidine