Only the target tissue (dispensable tissue) is mutant while the rest of the mouse stays viable and fertile
A system where an enzyme causes recombination at specific DNA target sites in somatic cells- not during mitosis
LoxP sites and Cre recombinase
Lox and Cre come from P1 phage
It recombines the loxP sites and deletes the DNA between them
Flanked by loxP sites
A mouse in which important exon(s) of a gene are flanked by loxP sites
Because deleting them will disrupt the gene and create a knockout in cells where Cre is expressed
Use CRISPR + HDR to insert one loxP site on each side of important exon(s) of YFG
Two guide RNAs and two donor DNAs
One targets one side of the exon and the other targets the other side
One donor inserts the first loxP site and the other donor inserts the second loxP site
Show YFG with important exon(s), Cas9 plus 2 gRNAs cutting on each side, 2 donor DNAs carrying loxP sites, HDR inserting both loxP sites, and the final floxed YFG allele
By pronuclear injection
A tissue-specific promoter driving Cre cDNA
It determines where Cre will be expressed
Cross the floxed YFG mouse with a transgenic Cre mouse that expresses Cre in a specific tissue
Cre deletes the floxed exon(s) only in the cells where the Cre promoter is active
Show a floxed YFG mouse crossed with a tissue-specific Cre mouse, then in double-transgenic offspring show Cre expressed only in the target tissue and deletion of the floxed exon only there
A floxed allele is still functional until Cre is expressed, while a conditional knockout is produced after Cre deletes the floxed exon(s) in specific cells
Phelan-McDermid syndrome
A contiguous gene disorder
22q13.3 : can be terminal or interstital
SHANK3
They connect receptors to the cytoskeleton at synapses
A Shank3 floxed strain
Most of the Shank3 gene, effectively exons 4 through 22
A CMV-Cre strain
A constitutive promoter active in most cells and tissues
Because Cre is expressed in most cells, including germ cells
By crossing the Shank3 floxed mouse with the CMV-Cre mouse so Cre deleted the loxP-flanked region
Cross the floxed YFG strain to a constitutive Cre strain, let Cre delete the loxP-flanked exon(s) in all cells, then breed and identify mice carrying the deleted YFG allele
To amplify specific DNA regions that differ between wild-type, floxed, and knockout alleles
Agarose gel electrophoresis
Separates PCR products by size so different alleles can be distinguished as different bands
Different primer pairs amplify different allele structures, so band presence and size reveal the genotype
Because it carries 2 different alleles that generate different PCR products
Two?
Show genomic DNA, primers flanking diagnostic regions, PCR amplification of allele-specific fragments, loading products on an agarose gel, and different band patterns for WT, heterozygote, and knockout
CRISPR to make the floxed allele, Cre/Lox to delete it, and PCR plus agarose gel electrophoresis to verify the genotype
KO mice were much slower than WT and heterozygotes, while heterozygotes were closer to WT
KO mice buried far fewer marbles than WT and heterozygotes, while heterozygotes were close to WT
Autosomal recessive-like for the measured mouse behavioral phenotypes
