Cytosine base editors induce off-target mutations and adverse phenotypic effects in transgenic mice.
Nana YanHu FengYongsen SunYing XinHaihang ZhangHongjiang LuJitan ZhengChenfei HeZhenrui ZuoTanglong YuanNana LiLong XieWu WeiYi-Di SunErwei ZuoPublished in: Nature communications (2023)
Base editors have been reported to induce off-target mutations in cultured cells, mouse embryos and rice, but their long-term effects in vivo remain unknown. Here, we develop a Systematic evaluation Approach For gene Editing tools by Transgenic mIce (SAFETI), and evaluate the off-target effects of BE3, high fidelity version of CBE (YE1-BE3-FNLS) and ABE (ABE7.10 F148A ) in ~400 transgenic mice over 15 months. Whole-genome sequence analysis reveals BE3 expression generated de novo mutations in the offspring of transgenic mice. RNA-seq analysis reveals both BE3 and YE1-BE3-FNLS induce transcriptome-wide SNVs, and the numbers of RNA SNVs are positively correlated with CBE expression levels across various tissues. By contrast, ABE7.10 F148A shows no detectable off-target DNA or RNA SNVs. Notably, we observe abnormal phenotypes including obesity and developmental delay in mice with permanent genomic BE3 overexpression during long-time monitoring, elucidating a potentially overlooked aspect of side effects of BE3 in vivo.
Keyphrases
- rna seq
- single cell
- poor prognosis
- gene expression
- type diabetes
- cell proliferation
- insulin resistance
- high fat diet induced
- induced apoptosis
- weight loss
- emergency department
- magnetic resonance
- genome wide
- long non coding rna
- circulating tumor
- signaling pathway
- oxidative stress
- copy number
- transcription factor
- weight gain
- cell cycle arrest
- pi k akt
- dna methylation
- circulating tumor cells
- adverse drug