Inducible Genome Editing with Conditional CRISPR/Cas9 Mice

G3 (Bethesda). 2018 May 4;8(5):1627-1635. doi: 10.1534/g3.117.300327.

Abstract

Genetically engineered mouse models (GEMMs) are powerful tools by which to probe gene function in vivo, obtain insight into disease etiology, and identify modifiers of drug response. Increased sophistication of GEMMs has led to the design of tissue-specific and inducible models in which genes of interest are expressed or ablated in defined tissues or cellular subtypes. Here we describe the generation of a transgenic mouse harboring a doxycycline-regulated Cas9 allele for inducible genome engineering. This model provides a flexible platform for genome engineering since editing is achieved by exogenous delivery of sgRNAs and should allow for the modeling of a range of biological and pathological processes.

Keywords: CRISPR/Cas9; Cas9 knock-in; conditional Cas9 mouse; genome editing; mouse model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • CRISPR-Cas Systems / genetics*
  • Doxycycline / pharmacology
  • Gene Editing*
  • Gene Expression / drug effects
  • Genetic Engineering
  • Genome*
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism
  • Mice
  • Mice, Transgenic
  • Models, Animal
  • Mouse Embryonic Stem Cells / drug effects
  • Mouse Embryonic Stem Cells / metabolism
  • Proto-Oncogene Proteins c-myc / metabolism
  • RNA, Guide, CRISPR-Cas Systems / genetics

Substances

  • Proto-Oncogene Proteins c-myc
  • RNA, Guide, CRISPR-Cas Systems
  • Doxycycline