Genotyping Genetically Modified (GM) Mice.
CRISPR/Cas9
Chimera
Genetically engineered mice
Genotyping
Germ line transmission
Knock-in mice
Knock-out mice
Mosaic
PCR
Targeted
Transgenic
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2020
2020
Historique:
entrez:
13
9
2019
pubmed:
13
9
2019
medline:
15
12
2020
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 31512214
doi: 10.1007/978-1-4939-9837-1_12
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
133-148Subventions
Organisme : NCI NIH HHS
ID : R50 CA211121
Pays : United States