Genotyping Genetically Modified (GM) Mice

Neeraj K. Aryal, Jan Parker-Thornburg

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations

Abstract

Prior to generating a new mouse model, it is important to plan the method that will be used to detect which of the mice generated have the mutation(s) desired. Nearly, all types of mutations may be detected using PCR. However, the choice of primers will differ depending upon the method used to generate the model. Transgenic mice should be genotyped across a unique junction fragment. Targeted ES cells used to generate knock-out or knock-in mice should be genotyped using primers from a unique marker in the construct and a region outside of the construct. Targeting in ES cells can also be detected using a genomic Southern blot. Mice targeted using CRISPR/Cas9 should have the region of interest amplified using PCR, and then be assessed for size changes (for large changes in sequence) by Surveyor Assay (for gene knock-out and point mutations) and/or sequenced to verify the mutation. Each of these models has a unique requirement for genotyping, and failure to understand the requirements can easily lead to loss of the gene in subsequent generations.

Original languageEnglish (US)
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages133-148
Number of pages16
DOIs
StatePublished - 2020

Publication series

NameMethods in Molecular Biology
Volume2066
ISSN (Print)1064-3745
ISSN (Electronic)1940-6029

Keywords

  • CRISPR/Cas9
  • Chimera
  • Genetically engineered mice
  • Genotyping
  • Germ line transmission
  • Knock-in mice
  • Knock-out mice
  • Mosaic
  • PCR
  • Targeted
  • Transgenic

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

MD Anderson CCSG core facilities

  • Genetically Engineered Mouse Facility

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