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Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Mating System Homozygote x Homozygote (Female x Male) 17-APR-08 Species laboratory mouse Generation N11+F5 (02-FEB-09) Donating Investigator Klaus Rajewsky, Immune Disease Institute (formerly CBRI) Description
Homozygous mutant mice are viable, fertile, normal in size, and do not display any gross physical or behavioral abnormalities. Homozygotes have a deficiency in the B-1 subset of B-lymphocytes along with a concomitant reduction in serum IgM. Their ability to respond to T-cell-dependent antigens is severely impaired, and they fail to form splenic germinal centers.In addition to disrupting the targeted gene, the targeting construct also introduced a cre cassette into exon 2 of the targeted gene, effectively placing cre expression under the control of the endogenous promoter. The Cd19 promoter specifically directs cre expression at the earliest stages and throughout B-lymphocyte development and differentiation. Although homozygous mutant mice are Cd19-deficient, heterozygous mice are phenotypically normal, and can be used for specific deletion of loxP-flanked (floxed) targets in B-lymphocytes.
In an attempt to offer alleles on well-characterized or multiple genetic backgrounds, alleles are frequently moved to a genetic background different from that on which an allele was first characterized. It should be noted that the phenotype could vary from that originally described. We will modify the strain description if necessary as published results become available.
Development
A targeting vector containing Cre recombinase, the rabbit beta-globin intron /poly A signal sequence, and an FRT-flanked neomycin resistance gene, was used to disrupt exon 2 of the Cd19 gene and to express cre under the regulation of the endogenous promoter. Herpes simplex virus thymidine kinase gene was placed 3' of the Cd19 sequence to allow for the selection against random integration. The construct was transfected into 129P2/OlaHsd-derived E14-1 embryonic stem cells. Correctly targeted ES cells were injected into 129/Sv blastocysts. The resulting chimeric animals were backcrossed to BALB/c IgHb congenics for a number of generations and then backcrossed to C57BL/6 for 10 generations.
| Control | ||
|---|---|---|
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
Strains carrying Cd19tm1(cre)Cgn allele
004126 C.Cg-Cd19tm1(cre)Cgn Ighb/J View Strains carrying Cd19tm1(cre)Cgn (1 strain)
Strains carrying other alleles of cre
View Strains carrying other alleles of cre (161 strains)
Introduction to Cre-lox technology
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Cd19tm1(cre)Cgn/Cd19tm1(cre)Cgn
involves: 129P2/OlaHsd
- hematopoietic system phenotype
- abnormal B cell differentiation (MGI Ref ID J:27463)
- absent spleen germinal center (MGI Ref ID J:27463)
- failure of germinal center formation
- decreased B-1 B cell number (MGI Ref ID J:27463)
- reduced numbers of B1 cells (cd23-, IgM hi, IgD lo)
- immune system phenotype
- abnormal B cell differentiation (MGI Ref ID J:27463)
- abnormal B cell physiology (MGI Ref ID J:27463)
- impaired Cd19-/- B cell response to T cell dependent antigens
- abnormal immunoglobulin level (MGI Ref ID J:27463)
- failure of affinity maturation of serum antibodies
- decreased IgM level (MGI Ref ID J:27463)
- reduction in serum IgM
- absent spleen germinal center (MGI Ref ID J:27463)
- failure of germinal center formation
- decreased B-1 B cell number (MGI Ref ID J:27463)
- reduced numbers of B1 cells (cd23-, IgM hi, IgD lo)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
cre relatedHematological Research
Hematopoietic Defects
Immunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency
B cell defects
Research Tools
Cre-lox System
Cre Recombinase Expression
Developmental Biology Research
Cre-lox System
Genetics Research
Mutagenesis and Transgenesis: Cre-lox System
Cd19tm1(cre)Cgn relatedResearch Tools
Cre-lox System
Hematological Research
Hematopoietic Defects
Immunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency
B cell defects
Research Tools
Genetics Research
Mutagenesis and Transgenesis: Cre-lox System
| Allele Symbol | Cd19tm1(cre)Cgn | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, University of Cologne | ||
| Allele Type | Targeted (knock-in) | ||
| Common Name(s) | CD19-; CD19-Cre; CD19-KO; Cd19Cre; Cd19cre; | ||
| Mutation Made By | Robert Rickert, The Burnham Institute | ||
| Strain of Origin | 129P2/OlaHsd | ||
| ES Cell Line Name | E14.1 | ||
| ES Cell Line Strain | 129P2/OlaHsd | ||
| Site of Expression | B cells | ||
| Expressed Gene | cre, cre recombinase, bacteriophage P1 | ||
| Cre recombinase is an enzyme derived from the bacteriophage P1 that specifically recognizes loxP sites. Cre has been shown to effectively mediate the excision of DNA located between loxP sites. After the excision event, the DNA ends recombine leaving a single loxP site in place of the intervening sequence. | |||
| Gene Symbol and Name | Cd19, CD19 antigen | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | AW495831; B4; MGC109570; MGC12802; expressed sequence AW495831; | ||
| Driver Note | Cd19 | ||
| Molecular Note | In frame insertion of a cre recombinase gene into the first coding exon followed by an frt-flanked neomycin cassette. A frameshift mutation was also introduced into exon 5. This allele expresses cre recombinase specifically in B lineage cells throughout development. [MGI Ref ID J:27463] | ||
Genotyping Protocols
Cd19tm1(cre)Cgn, Melt Curve Analysis
Cd19tm1(cre)Cgn, Separated PCR
Helpful Links
Genotyping resources and troubleshooting
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Animal Health Reports
Room Number AX11
Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice may be bred as heterozygotes or homozygotes. The donating investigator reports that homozygotes older than 3 months of age do not breed well. Homozygous breeding pairs maintained at The Jackson Laboratory have shown no such problems. Mating System Homozygote x Homozygote (Female x Male) 17-APR-08 Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
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Weeks of Age Price (US dollars $) Gender Genotypes Provided Individual Mouse $160.40 Female or Male Homozygous for Cd19tm1(cre)Cgn
Pairs /Price (US dollars $) Pair Genotype $320.80 Homozygous for Cd19tm1(cre)Cgn x Homozygous for Cd19tm1(cre)Cgn
| Pricing for International shipping destinations |
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Weeks of Age Price (US dollars $) Gender Genotypes Provided Individual Mouse $208.60 Female or Male Homozygous for Cd19tm1(cre)Cgn
Pairs /Price (US dollars $) Pair Genotype $417.10 Homozygous for Cd19tm1(cre)Cgn x Homozygous for Cd19tm1(cre)Cgn
| Standard Supply | Repository-Live. A collection of over 1000 strains maintained as live colonies. Individual colonies are sized to meet current customer demand. Delivery for orders of 10 mice or less ranges on average from one to eight weeks; mice are generally shipped between four to six weeks of age with a maximum shipping age of approximately nine weeks. Colony sizes do not generally support stringent age specifications for large volumes of mice; however custom orders and larger quantities of mice are easily arranged. Estimated ship dates for all orders provided within two business days following order placement. |
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| Supply Notes |
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| Control | ||
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| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
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