"knockout mouse" homologous recombination A knockout mouse has had both alleles of a particular gene replaced with an inactive allele. This is usually accomplished by using homologous recombination to replace one allele followed by two or more generations of selective breeding until breeing pairs are isolated that have both alleles of the targeted gene inactivated or knocked out.

When an investigator wants to replace one allele with an engineered construct but not affect any other locus in the genome, then the method of choice is homologous recombination. To perform homolgous recombination, you must know the DNA sequence of the gene you want to replace. With this information, it is possible to replace any gene with a DNA construct of your choosing. The next step is to design and fabricate the DNA construct you want to insert into the chromosome in place of the wild-type allele. This construct may contain any DNA sequence of your choosing which means you can insert different alleles (both functional and non-functional ones), different genes or reporter genes (e.g. antibiotic resistance or green fluorescent protein). Regardless of what you want to insert, you must include some flanking DNA that is identical in sequence to the targeted locus

negative selection marker (e.g. thymidine kinase, tk) is added to the In addition to the positive selection marker (e.g. antibiotic resistance) often a negative selection marker (e.g. thymidine kinase, tk) is added to the replacement vector. The negative marker is outside the region of sequence similarity between the vector and the targeted locus. The engineered construct is added to cells which contain the targeted gene of interest. By mechanisms that are poorly understood but are similar to what occurrs during meiosis and mitosis when homolgous chromosomes align along the metaphase plane, the engineered construct finds the targeted gene and recombination takes place within the homolgous (meaning identical in this case) sequences. Once the cells have performed their part of the procedure, the end result is a new piece of DNA inserted into the chromosome. The rest of the genome is unaltered but the single targeted locus has been replaced with the engineered construct and some of its flanking DNA .

incorporated into the genome. If the targeting vector aligns in a non-homologous region of the genome, then recombination is random and the negative selection marker may become incorporated into the genome. The final product of non-homologous recombination can survive positive (antibiotic) selection. However, there is a drug called gancyclovir that will kill any cell that contains the tk gene. So cells undergoing homologous recombination are grown in antibiotic to select for recombination and gancyclovir to kill any cells that successfully conducted non-homologous recombination. The positive and negative selection markers are incorporated into chromosome so gancyclovir will kill cells with modified chromosomes.

A knockout mouse has had both alleles of a particular gene replaced with an inactive allele.. 1. 2. Isolate developing embryo at blastocyst stage. This embryo is from a strain of mice with gray fur. Transfect stem cells with homologous recombination construct. Select for homologous recombination by growing stem cells in neomycin and gancyclvir. Remove embryonic stem cells from gray-fur blastocyst. Grow stem cells in tissue culture.

Implant several chimeric blastocysts into pseudo-pregnant, white fur mouse. Mother will give birth to a range of mice. Some will be normal white fur mice but others will be chimeric mice. Chimeric mice have many of their cells from the original white fur blastocyst but some of their cells will be derived from recombinant stem cells. Fur cells from recombinant stem cells produce gray patches which are easily detected.

Mate the chimeric mice with wild-type white fur mice. If the gonads of the chimeric mice were derived from recombinant stem cells, all the offspring will have gray fur. Every cell in gray mice are heterozygous for the homologous recombination. Mate heterozygous gray mice (+/ H) and genotpye the gray offspring. Identify homozygous recombinants (H / H) and breed them to produce a strain of mice with both alleles knocked out. The pure breeding mouse strain is a "knockout mouse".

Knock in módszer Engrailed 1 és 2 egér homeobox gének. En-1 ko egér: súlyos fejlôdési rendellenességek. En-2 ko egér OK. En-1 kompenzál? És En-2? Az En-2 az En-1 promoter kontrollja alá került. En-1 hamarabb expresszálódik, mint En-2. Az En-1/En2 knock in egér OK, tehát az En-2 képes helyettesíteni az En-t.

Bone marrow transplantation +Mx -Mx Granulocita és monocita irrad. wt rec. ko donor B- és T- limfocita

Az egér füle k.o. k.o. k.o. k.o. +/+ Lucerna-tart. táp Pheophorbide a is transported by BCRP Lucerna-tart. táp

Az egér füle +/+ k.o. Bone marrow transplantation Lucerna táp

"knockout mouse"