Collin G Johnson1,2, Tong Chen3,4, Nika Furey2,4, Madeline G Hemmingsen1,4, Karl-Dimiter Bissig1,2,3,4,5. 1. Center for Cell and Gene Therapy, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, Texas. 2. Department of Molecular & Cellular Biology, Baylor College of Medicine, Houston, Texas. 3. Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, Texas. 4. Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina. 5. Duke Cancer Institute, Duke University, Durham, North Carolina.
Abstract
Somatic liver knockout (SLiK) is a method developed to rapidly generate a liver-specific knockout of one or several genes. This technique combines the strengths of CRISPR/Cas9 gene editing and hydrodynamic tail-vein injection, a simple in vivo method for transfection of hepatocytes, to harness the powerful selection pressure of tyrosinemic livers to replace host hepatocytes with any desired gene deletion. In this protocol, we will describe sgRNA design and cloning, hydrodynamic tail-vein injection of targeting constructs, and screening and validation methods for efficient in vivo gene editing.
Somatic liver knockout (SLiK) is a method developed to rapidly generate a liver-specific knockout of one or several genes. This technique combines the strengths of CRISPR/Cas9 gene editing and hydrodynamic tail-vein injection, a simple in vivo method for transfection of hepatocytes, to harness the powerful selection pressure of tyrosinemic livers to replace host hepatocytes with any desired gene deletion. In this protocol, we will describe sgRNA design and cloning, hydrodynamic tail-vein injection of targeting constructs, and screening and validation methods for efficient in vivo gene editing.
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