A mutation-independent CRISPR-Cas9-mediated gene targeting approach to treat a murine model of ornithine transcarbamylase deficiency.
Lili WangYang YangCamilo BretonPeter BellMingyao LiJia ZhangYan CheAlexei SavelievZhenning HeJohn WhiteCaitlin LatshawChenyu XuDeirdre McMenaminHongwei YuHiroki MorizonoMark L BatshawJames M WilsonPublished in: Science advances (2020)
Ornithine transcarbamylase (OTC) deficiency is an X-linked urea cycle disorder associated with high mortality. Although a promising treatment for late-onset OTC deficiency, adeno-associated virus (AAV) neonatal gene therapy would only provide short-term therapeutic effects as the non-integrated genome gets lost during hepatocyte proliferation. CRISPR-Cas9-mediated homology-directed repair can correct a G-to-A mutation in 10% of OTC alleles in the livers of newborn OTC spfash mice. However, an editing vector able to correct one mutation would not be applicable for patients carrying different OTC mutations, plus expression would not be fast enough to treat a hyperammonemia crisis. Here, we describe a dual-AAV vector system that accomplishes rapid short-term expression from a non-integrated minigene and long-term expression from the site-specific integration of this minigene without any selective growth advantage for OTC-positive cells in newborns. This CRISPR-Cas9 gene-targeting approach may be applicable to all patients with OTC deficiency, irrespective of mutation and/or clinical state.
Keyphrases
- crispr cas
- gene therapy
- genome editing
- late onset
- poor prognosis
- replacement therapy
- genome wide
- end stage renal disease
- early onset
- public health
- long non coding rna
- binding protein
- chronic kidney disease
- ejection fraction
- copy number
- induced apoptosis
- pregnant women
- signaling pathway
- cancer therapy
- drug delivery
- metabolic syndrome
- oxidative stress
- gene expression
- type diabetes
- skeletal muscle
- cell cycle arrest
- insulin resistance
- pi k akt
- adipose tissue
- genome wide identification
- coronary artery disease
- endoplasmic reticulum stress
- cord blood
- transcription factor