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Strain Name: |
C.129S(B6)-Stat5atm1Mam/J |
Stock Number: |
007806 |
Availability:
| Repository- Live |
Product Information
Strain Details
| Type |
JAX® GEMM® Strain -
Congenic |
| Additional information on
JAX® GEMM® Strains. |
| Type |
JAX® GEMM® Strain -
Mutant Strain |
| Type |
JAX® GEMM® Strain -
Targeted Mutation |
| Mating System | Heterozygote x Heterozygote
(Female x Male) |
|---|
| |
| Species | laboratory mouse |
| Donating Investigator | Michael Tomasson, Washington University School of Medicine |
| Generation | N5+
(05-AUG-08)
|
|
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Strain Description
Mice homozygous for the targeted mutation are viable, develop normally, and are fertile, but females do not lactate. Mammary ductal development through pregnancy is normal, but lobuloalveolar development is severely reduced, and milk is not secreted even after prolonged suckling. Levels of the closely-related STAT5B protein are also markedly reduced in STAT5A-deficient mice, but STAT5B protein levels increase and phosphorylation is evident after 3 days of suckling. Expression of several milk protein genes is unaffected in homozygous mutants, but whey acidic protein expression is severely reduced. Homozygous males exhibit abnormal prostate morphology and an increase in probasin secretion. Immmunological defects exhibited by homozygotes include a reduced number of peritoneal mast cells, decreased IL-3-dependent development of bone marrow-derived mast cells, defective bone marrow-derived macrophage GM-CSF (Granulocyte-Macrophage Colony-Stimulating Factor)-induced proliferation, decreased number of NK cells, and decreased expansion of T cells. This mutant mouse strain may be useful in studies of mammary gland development, lactogenesis, hematopoiesis, and immunological intracellular signal transduction.
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. This is the case for the strain above. 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.
Strain Development
A targeting vector containing phosphoglycerate kinase promoter-driven neomycin resistance gene casette and a herpes simplex virus thymidine kinase gene was used to disrupt a region containing a non-coding exon, 2 coding exons and flanking sequence. The construct was electroporated into 129S6/SvEvTac derived TC-1 embryonic stem (ES) cells, and correctly targeted ES cells were injected into C57BL/6J blastocysts. The resulting chimeric animals were crossed to 129 mice, and then backcrossed to C57BL/6 for one generation. The donating investigator backcrossed the strain to BALB/cAnNTac for 3 generations using a marker-assisted protocol. The mice were subsequently backcrossed to BALB/cJ for a single generation.
Mammalian Phenotype Terms assigned by genotype
Stat5atm1Mam/Stat5atm1Mam
C.129S6-Stat5atm1Mam
- immune system phenotype
- abnormal mast cell morphology
(MGI Ref ID J:101855)
- IL-3-induced but not stem cell factor-induced proliferation of bone marrow derived mast cells is significantly diminished
- survival rates of both peritoneal mast cells and bone marrow derived mast cells are decreased and apoptotic cells are increased
- abnormal mast cell differentiation
(MGI Ref ID J:101855)
- the IL-3-dependent development of bone marrow derived mast cells is decreased
- decreased mast cell number
(MGI Ref ID J:101855)
- decrease in the number of mast cells in the peritoneal cavity, ear and stomach
- hematopoietic system phenotype
- abnormal mast cell morphology
(MGI Ref ID J:101855)
- IL-3-induced but not stem cell factor-induced proliferation of bone marrow derived mast cells is significantly diminished
- survival rates of both peritoneal mast cells and bone marrow derived mast cells are decreased and apoptotic cells are increased
- abnormal mast cell differentiation
(MGI Ref ID J:101855)
- the IL-3-dependent development of bone marrow derived mast cells is decreased
- decreased mast cell number
(MGI Ref ID J:101855)
- decrease in the number of mast cells in the peritoneal cavity, ear and stomach
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Stat5atm1Mam/Stat5atm1Mam
either: 129S6/SvEvTac-Stat5atm1Mam or (involves: 129S6/SvEvTac * NIH Black Swiss)
- endocrine/exocrine gland phenotype
- abnormal lactation
(MGI Ref ID J:64278)
- females fail to lactate after parturition because of a failure of terminal differentiation
- continued suckling does not result in milk production and release, however expression of milk protein genes and synthesis of milk proteins is maintained and the gland does not involute
- abnormal mammary gland development
(MGI Ref ID J:64278)
- abnormal branching of the mammary ductal tree
(MGI Ref ID J:64278)
- ductal development appears normal but lobuloalveolar outgrowth is severely reduced, secretory tissue is sparse, and alveoli are petite and contain small lumina
- abnormal mammary gland growth during lactation
(MGI Ref ID J:64278)
- lubuloalveolar units are underdeveloped and do not exhibit a secretory phenotype, even after maximal stimulation of prolactin secretion induced by suckling
- abnormal mammary gland growth during pregnancy
(MGI Ref ID J:64278)
- mammary lobuloalveolar outgrowth during pregnancy is curtailed
- reproductive system phenotype
- abnormal lactation
(MGI Ref ID J:64278)
- females fail to lactate after parturition because of a failure of terminal differentiation
- continued suckling does not result in milk production and release, however expression of milk protein genes and synthesis of milk proteins is maintained and the gland does not involute
- abnormal mammary gland development
(MGI Ref ID J:64278)
- abnormal branching of the mammary ductal tree
(MGI Ref ID J:64278)
- ductal development appears normal but lobuloalveolar outgrowth is severely reduced, secretory tissue is sparse, and alveoli are petite and contain small lumina
- abnormal mammary gland growth during lactation
(MGI Ref ID J:64278)
- lubuloalveolar units are underdeveloped and do not exhibit a secretory phenotype, even after maximal stimulation of prolactin secretion induced by suckling
- abnormal mammary gland growth during pregnancy
(MGI Ref ID J:64278)
- mammary lobuloalveolar outgrowth during pregnancy is curtailed
Stat5atm1Mam/Stat5atm1Mam
involves: 129S6/SvEvTac
- endocrine/exocrine gland phenotype
- abnormal prostate morphology
(MGI Ref ID J:63495)
- on average, 10.6% show cystic prostates compared to 1% in wild type, however do not show changes in prostate size or epithelial hyperplasia
- abnormal prostate epithelium morphology
(MGI Ref ID J:63495)
- prostate is characterized by an increased prevalence of local disorganization within acinar epithelium of ventral prostates
- affected acini are filled with desquamated, granular epithelial cells that become embedded in dense, coagulated secretory material, resulting in glandular cyst formation
- abnormal prostate physiology
(MGI Ref ID J:63495)
- exhibit an increase in prostate secretion of probasin
- reproductive system phenotype
- abnormal prostate morphology
(MGI Ref ID J:63495)
- on average, 10.6% show cystic prostates compared to 1% in wild type, however do not show changes in prostate size or epithelial hyperplasia
- abnormal prostate epithelium morphology
(MGI Ref ID J:63495)
- prostate is characterized by an increased prevalence of local disorganization within acinar epithelium of ventral prostates
- affected acini are filled with desquamated, granular epithelial cells that become embedded in dense, coagulated secretory material, resulting in glandular cyst formation
- abnormal prostate physiology
(MGI Ref ID J:63495)
- exhibit an increase in prostate secretion of probasin
Stat5atm1Mam/Stat5atm1Mam
involves: 129S6/SvEvTac * C57BL/6
- immune system phenotype
- abnormal spleen cellularity
(MGI Ref ID J:112035)
- exhibit decreased numbers of splenocytes
- decreased NK cell number
(MGI Ref ID J:112035)
- the percentage of NK cells is diminished (about 70% of the percentage seen in wild type) although to a lesser extent than in Stat5btm1Hwd homozygotes
- impaired NK cell cytolysis
(MGI Ref ID J:112035)
- NK cytolytic activity is impaired but to a lesser extent than seen in Stat5btm1Hwd homozygotes
- hematopoietic system phenotype
- abnormal spleen cellularity
(MGI Ref ID J:112035)
- exhibit decreased numbers of splenocytes
- decreased NK cell number
(MGI Ref ID J:112035)
- the percentage of NK cells is diminished (about 70% of the percentage seen in wild type) although to a lesser extent than in Stat5btm1Hwd homozygotes
|
Gene & Allele Details
| Allele Symbol |
Stat5atm1Mam |
| Allele Name |
targeted mutation 1, Lothar Hennighausen |
| Common Name(s) |
Stat5a-;
|
| Mutation Made By | Lothar Hennighausen, National Institutes of Health |
| Strain of Origin | 129S6/SvEvTac |
| ES Cell Line Name | TC-1 |
| ES Cell Line Strain | 129S6/SvEvTac |
| Gene Symbol and Name |
Stat5a, signal transducer and activator of transcription 5A |
| Chromosome |
11 |
| Gene Common Name(s) |
AA959963;
MGF;
STAT5;
expressed sequence AA959963;
|
| Molecular Note |
The promoter sequence, an untranslated exon, and two coding exons were replaced by a neomycin selection cassette. Western blot analysis of extracts immunoprecipitated from mammary tissue of homozygous mutant mice showed an absence of encoded protein. [MGI Ref ID J:64278]
|
Control Information
Genotyping Protocols
Stat5atm1Mam
Colony Maintenance
| Breeding & Husbandry | When maintaining a live colony, these mice are bred heterozygous females x homozygous males. Although homozygous females are viable and fertile, they do not lactate. Litters from homozygous females must be fostered. |
| Diet Information |
LabDiet® 5K52/5K67
|
Related Strains
Strains carrying Stat5atm1Mam allele
View Strains carrying Stat5atm1Mam (2 strains)
Additional Web Information
Congenic Nomenclature
Animal Health Reports
Room Number AX12
Research Applications
This mouse can be used to support research in many areas including:
Cancer Research
Genes Regulating Growth and Proliferation
Hematological Research
Mast Cell Deficiency
Immunology and Inflammation Research
Immunodeficiency
(NK Cell Deficiency)
Immunodeficiency
(T cell deficiency)
Intracellular Signaling Molecules
Stat5atm1Mam related
Cancer Research
Genes Regulating Growth and Proliferation
Immunology and Inflammation Research
Immunodeficiency
(Mast Cell Deficiency)
Intracellular Signaling Molecules
Research Tools
Immunology and Inflammation Research
(Mast Cell Deficiency)
References
Selected Reference(s)
Liu X; Robinson GW; Wagner KU; Garrett L; Wynshaw-Boris A; Hennighausen L. 1997. Stat5a is mandatory for adult mammary gland development and lactogenesis. Genes Dev
11(2):179-86.
[PubMed: 9009201]
[MGI Ref ID J:64278]
Additional References
Price and Supply Information
| Strain Name: |
C.129S(B6)-Stat5atm1Mam/J |
| Stock Number: |
007806 |
Price Details
IMPORTANT NOTE: Prices are based on shipping destination.
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Supply Details
| 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 ~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 48 hours of order placement. |
| Supply Notes |
Usually shipped between four and eight weeks of age.
This strain is included in the Induced Mutant Resource Colony collection.
|
| Licensing | See General Terms and Conditions below
|
| Control Information | View Control Information in Strain Details.
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|---|
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® Mice strains as
well as the genotypes of strains with identified molecular mutations.
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® Mice strains are only made available to researchers after meeting our
standards. However, the phenotype of each strain may not be fully
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Therefore, we
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ensure that JAX
® Mice will meet the needs of individual research projects
or when requesting a strain that is new to your research, we suggest ordering
and performing tests on a small number of mice to determine suitability for
your particular project.
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