Multiplex ligation-dependent probe amplification for identification of correctly targeted murine embryonic stem cell clones

Anal Biochem. 2015 Apr 1:474:35-7. doi: 10.1016/j.ab.2015.01.007. Epub 2015 Jan 20.

Abstract

Following locus-specific genome editing of mouse embryonic stem cells (ESCs), the identification of correctly targeted clones remains a challenge. We applied multiplex ligation-dependent probe amplification (MLPA) to screen for homologous recombination-based genomic integration of a knockout construct in which part of a gene is deleted. All candidate ESCs thereby identified were subsequently validated by conventional methods. Thus, MLPA represents a highly reliable as well as cost- and time-efficient alternative to currently applied methods such as Southern blotting and polymerase chain reaction (PCR)-based approaches. It is also applicable to knockin recombination strategies and compatible with the CRISPR/Cas9 system and other genome editing strategies.

Keywords: Embryonic stem cells; Genome engineering; Knockout; MLPA; Mouse model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Clone Cells
  • Electroporation
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / metabolism
  • Homologous Recombination / genetics
  • Membrane Proteins / deficiency
  • Membrane Proteins / metabolism
  • Mice, Knockout
  • Multiplex Polymerase Chain Reaction / methods*

Substances

  • Membrane Proteins
  • REEP2 protein, mouse