Human 8-cell embryos enable efficient induction of disease-preventive mutations without off-target effect by cytosine base editor

Protein Cell. 2023 Jun 7;14(6):416-432. doi: 10.1093/procel/pwac043.

Abstract

Approximately 140 million people worldwide are homozygous carriers of APOE4 (ε4), a strong genetic risk factor for late onset familial and sporadic Alzheimer's disease (AD), 91% of whom will develop AD at earlier age than heterozygous carriers and noncarriers. Susceptibility to AD could be reduced by targeted editing of APOE4, but a technical basis for controlling the off-target effects of base editors is necessary to develop low-risk personalized gene therapies. Here, we first screened eight cytosine base editor variants at four injection stages (from 1- to 8-cell stage), and found that FNLS-YE1 variant in 8-cell embryos achieved the comparable base conversion rate (up to 100%) with the lowest bystander effects. In particular, 80% of AD-susceptible ε4 allele copies were converted to the AD-neutral ε3 allele in human ε4-carrying embryos. Stringent control measures combined with targeted deep sequencing, whole genome sequencing, and RNA sequencing showed no DNA or RNA off-target events in FNLS-YE1-treated human embryos or their derived stem cells. Furthermore, base editing with FNLS-YE1 showed no effects on embryo development to the blastocyst stage. Finally, we also demonstrated FNLS-YE1 could introduce known protective variants in human embryos to potentially reduce human susceptivity to systemic lupus erythematosus and familial hypercholesterolemia. Our study therefore suggests that base editing with FNLS-YE1 can efficiently and safely introduce known preventive variants in 8-cell human embryos, a potential approach for reducing human susceptibility to AD or other genetic diseases.

Keywords: APOE4; base editor; disease-preventive mutations; human embryo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoprotein E4* / genetics
  • Blastocyst
  • CRISPR-Cas Systems
  • Cytosine*
  • Gene Editing
  • Heterozygote
  • Humans
  • Mutation

Substances

  • Apolipoprotein E4
  • Cytosine