4.7 Article

Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control

Journal

METHODS
Volume 121, Issue -, Pages 68-76

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2017.03.016

Keywords

CRISPR; Cas9; Genome editing; Screening; Genotyping; Mouse; Mutant; QC

Funding

  1. Medical Research Council IMPC Strategic Award [53658]
  2. National Institute for Health [U42OD011174]
  3. MRC [MC_UP_1502/1] Funding Source: UKRI
  4. Medical Research Council [MC_UP_1502/1] Funding Source: researchfish

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The application of CRISPR/Cas9 technology has revolutionised genetics by greatly enhancing the efficacy of genome editing in the early embryo. Furthermore, the system has enabled the generation of allele types previously incompatible with in vivo mutagenesis. Despite its versatility and ease of implementation, CRISPR/Cas9 editing outcome is unpredictable and can generate mosaic founders. Therefore, careful genotyping and characterisation of new mutants is proving essential. The literature presents a wide range of protocols for molecular characterisation, each representing different levels of investment. We present strategies and protocols for designing, producing and screening CRISPR/Cas9 edited founders and genotyping their offspring according to desired allele type (indel, point mutation and deletion). (C) 2017 The Authors. Published by Elsevier Inc.

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