Strain Name: |
C57BL/6J-Lystbg-J/J |
|---|---|
Stock Number: |
000629 |
Availability: | Level 4 |
General Terms and Conditions |
| Genes & Alleles | Lyst; Lystbg-J; |
Type JAX® GEMM® Strain - Coisogenic Additional information on JAX® GEMM® Strains. Type JAX® GEMM® Strain - Mutant Strain Type JAX® GEMM® Strain - Spontaneous Mutation Mating System Homozygote x Homozygote (Female x Male) Species laboratory mouse Generation N11F6 (03-JAN-08) Appearance
dark gray, affected
Related Genotype: a/a Lystbg-J/Lystbg-J
black, unaffected
Related Genotype: a/a Lystbg-J/+Strain Description
Mice homozygous for the beige-J spontaneous mutation (Lystbg-J) are identical to the original beige mutation (Lystbg). The phenotype closely resembles Chediak-Higashi disease in man and similar conditions in mink and cattle. Abnormal giant lysosomal granules occur in all tissues with granule-containing cells, including granulocytes, lymphocytes, cells of the liver, kidney, central nervous system, pancreas, and thyroid, and the ducts of most glands; in type II pneumocytes; in mast cells; and in retinal pigment epithelium. Granulocytes from beige homozygous mutant mice mice show defective chemotaxis and reduced bactericidal activity. Beige mice are more susceptible than controls to pneumonitis and to various viral, bacterial, and parasitic infections. Natural killer (NK) cells from beige mice exhibit decreased endogenous cytotoxic activity. Beige mice also have a defective cytotoxic T-cell and cytotoxic antibody response to allogeneic tumor cells. Syngeneic tumor cells grow better in beige mice than in littermate controls, an effect thought to be due to the deficiency of NK cells. Beige mice have platelet storage pool deficiency, leading to a prolonged bleeding time. The immunodeficiency of beige mutant mice has been used, especially in combination with the scid mutation (Prkdcscid), in tissue graft and disease studies.
Mammalian Phenotype Terms assigned by genotype |
| Allele Symbol | Lystbg-J | ||
|---|---|---|---|
| Allele Name | beige Jackson | ||
| Common Name(s) | bgj; | ||
| Strain of Origin | C57BL/6J | ||
| Gene Symbol and Name | Lyst, lysosomal trafficking regulator | ||
| Chromosome | 13 | ||
| Gene Common Name(s) | Beige; CHS; CHS1; D13Sfk13; DNA segment, Chr 13, Stephen F. Kingsmore 13; beige; bg; | ||
| General Note | This remutation occurred spontaneously in the C57BL/6J strain at The Jackson Laboratory (J:5311). It has essentially identical effects to the original Lystbg mutation, and has been used extensively in defining locus effects. | ||
| Molecular Note | This allele is defined by a noncomplementation test with Lystbg. Although mice homozygous for this allele show a decrease in Lyst mRNA in the liver compared to normal, the molecular basis for this allele is not yet known. [MGI Ref ID J:7539] | ||
| Allele | Control | |
|---|---|---|
| Lystbg-J | 000664 C57BL/6J | |
| Considerations for Choosing Controls | ||
| Diet Information | LabDiet® 5K52/5K67 |
|---|
Strains carrying Lystbg-J allele
000604 B6C3 a/A-T(10;13)199H +/+ Lystbg-J/J or Lystbg-2J/J View Strains carrying Lystbg-J (1 strain)
Strains carrying other alleles of Lyst
000204 B6.Cg-Lystbg/J 000604 B6C3 a/A-T(10;13)199H +/+ Lystbg-J/J or Lystbg-2J/J 000509 C3H/HeJ-Lystbg-2J/J 000494 J.Cg-Oca2+ Tyr+ Lystbg/J 000269 SB/LeJ View Strains carrying other alleles of Lyst (5 strains)
Genetic Quality Control Annual Report
JAX® NOTES, Spring 1991; 445. Why C57BL/6J-bgJ (beige) Mice are not Beige.
JAX® NOTES, Spring 2003; 489. Role of NK and NKT Cells in Immunity and Disease.
JAX® NOTES, Winter 1992; 448. The Beige (BgJ) Mutation.
Room Number AX30
Lystbg-J related
Cardiovascular Research
Atherosclerosis
Dermatology Research
Color and White Spotting Defects
Hematological Research
Immunological Defects
Platelet Defects (platelet storage pool deficiency)
Immunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency (NK Cell and Cd8 T Cell defects)
Immunodeficiency Associated with Other Defects
Intracellular Signaling Molecules
Internal/Organ Research
Kidney Defects (lysosomal enzyme abnormalities)
Metabolism Research
Mouse/Human Gene Homologs
Chediak-Higashi syndrome
Research Tools
Immunology and Inflammation Research (NK Cell Deficiency)
Selected Reference(s)
Additional ReferencesGallin JI; Bujak JS; Patten E; Wolff SM. 1974. Granulocyte function in the Chediak-Higashi syndrome of mice. Blood 43(2):201-6. [PubMed: 4589319] [MGI Ref ID J:5405]
Perou CM; Moore KJ; Nagle DL; Misumi DJ; Woolf EA; McGrail SH; Holmgren L; Brody TH; Dussault BJ Jr; Monroe CA; Duyk GM; Pryor RJ; Li L; Justice MJ; Kaplan J. 1996. Identification of the murine beige gene by YAC complementation and positional cloning. Nat Genet 13(3):303-8. [PubMed: 8673129] [MGI Ref ID J:33734]
Roder JC. 1979. The beige mutation in the mouse. I. A stem cell predetermined impairment in natural killer cell function. J Immunol 123(5):2168-73. [PubMed: 489978] [MGI Ref ID J:6213]
| Strain Name: | C57BL/6J-Lystbg-J/J |
| Stock Number: | 000629 |
IMPORTANT NOTE: Prices are based on shipping destination. To view prices, select your shipping destination.
| Standard Supply | Level 4. Up to 10 mice. Larger quantities or custom orders arranged upon request. Expected delivery up to one to three months. |
|---|---|
| Supply Notes |
Shipped at a specific age in weeks. Mice at a precise age in days, littermates and retired breeders are also available. Strains that must be genotyped are not available until five to seven weeks of age. Genomic DNA is available for this strain from the Mouse DNA Resource. |
| Licensing | See General Terms and Conditions below |
| Control Information | View Control Information in Strain Details. |
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