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| At 5 to 6 weeks of age, mice that are homozygous for this targeted mutation have a reduced number (approximately 68% of wildtype levels) of naive T cells in the spleen. This mutant mouse strain may be useful in studies of glycosidic molecular interactions and function. This strain was transferred from the collection of the Consortium for Functional Glycomics. | |||||||||||||||
Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Species laboratory mouse Generation F5+N1F1pN1 Donating Investigator Steve Rosen, University of San Francisco Description
Mice that are homozygous for the targeted mutation are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities. No gene product (mRNA) is detected by Northern blot analysis of total spleen RNA. Protein activity is not detected in spleen, lung peripheral lymph nodes, mesenteric lymph nodes or Peyer's patches. At 5 to 6 weeks of age, homozygotes have a reduced number (approximately 68% of wildtype levels) of naive T cells in the spleen. Chondroitin sulfate D is not detected in the brains of adult homozygotes or in the telencephalon and cartilage of homozygote embryos aged 12.5 and 15.5 embryonic days. Brain development is not impaired in mutant mice. This mutant mouse strain may be useful in studies of glycosidic molecular interactions and function.This strain was transferred from the collection of the Consortium for Functional Glycomics.
Development
A targeting vector containing neomycin resistance and diphtheria toxin fragment A genes was used to disrupt the portion of exon 3 that encodes the catalytic domain. The construct was electroporated into 129S2/SvPas derived D3 embryonic stem (ES) cells. Correctly targeted ES cells were injected into C57BL/6J blastocysts. The resulting chimeric animals were crossed to 129/SvJ mice, and then backcrossed to the same for 4 generations before being made homozygous. The mice were then backcrossed to C57BL/6 for 12 generations before arriving at The Jackson Laboratory.
| Control | ||
|---|---|---|
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
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.
Chst3tm1Tmu/Chst3tm1Tmu
involves: 129S2/SvPas * 129X1/SvJ
- immune system phenotype
- decreased T cell number (MGI Ref ID J:73698)
- reduction in number of naive T cells in the spleen of 5-6 week old mutant animals
- however, normal spleen morphology and lymphocyte trafficking into secondary lymph nodes
- nervous system phenotype
- *normal* nervous system phenotype (MGI Ref ID J:73698)
- normal brain development and morphology, particularly the organization of the cerebral cortex and orientation of processes for pyramidal cells
- hematopoietic system phenotype
- decreased T cell number (MGI Ref ID J:73698)
- reduction in number of naive T cells in the spleen of 5-6 week old mutant animals
- however, normal spleen morphology and lymphocyte trafficking into secondary lymph nodes
| Allele Symbol | Chst3tm1Tmu | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Takashi Muramatsu | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | C6st-; | ||
| Mutation Made By | Peter Sobieszczuk, Consortium for Functional Glycomics,TSRI | ||
| Strain of Origin | 129S2/SvPas | ||
| ES Cell Line Name | D3 | ||
| ES Cell Line Strain | 129S2/SvPas | ||
| Gene Symbol and Name | Chst3, carbohydrate (chondroitin 6/keratan) sulfotransferase 3 | ||
| Chromosome | 10 | ||
| Gene Common Name(s) | C6ST; C6ST-1; C6ST1; GST-0; HSD; | ||
| Molecular Note | A neomycin resistance cassette replaced sequences in exon III encoding part of the catalytic domain. Northern blot analysis of spleen did not detect mRNA in homozygous mutant mice. Protein activity was not detected in spleen, lung, and lymph nodes of homozygous mutant mice. [MGI Ref ID J:73698] | ||
Genotyping Protocols
Chst3tm1Tmu, SEP PCR, vers. 1
Helpful Links
Genotyping resources and troubleshooting
Uchimura K; Kadomatsu K; Nishimura H; Muramatsu H; Nakamura E; Kurosawa N; Habuchi O; El-Fasakhany FM; Yoshikai Y; Muramatsu T. 2002. Functional analysis of the chondroitin 6-sulfotransferase gene in relation to lymphocyte subpopulations, brain development, and oversulfated chondroitin sulfates. J Biol Chem 277(2):1443-50. [PubMed: 11696535] [MGI Ref ID J:73698]
Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice can be bred as homozygotes.
| Pricing for USA, Canada and Mexico shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Standard Supply | Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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| Control | ||
|---|---|---|
| 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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| phone: | 207-288-6470 |
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