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Former Names C.129S6(B6)-Epha2tm1Jrui/J (Changed: 28-FEB-06 ) 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 Donating Investigator IMR Colony, The Jackson Laboratory Description
Mice homozygous for this targeted mutation are viable, fertile, and display no overt developmental or behavioral abnormalities. In mutant mice of a mixed BALB/c, C57BL/6, and 129S6 background, murine pulmonary microvascular endothelial cells (MPMECs) isolated from homozygotes express no endogenous protein. MPMECs from Epha2-deficient mice show impaired ephrin-A1-induced vascular assembly and defective migration both in vitro and in vivo. In addition, MPMECs from homozygous Epha2 mice exhibit decreased angiogenesis and fail to activate Rac1 in response to ephrin-A1 in vivo. Mutant mice on a BALB/c background that were transplanted with metastatic mammary adenocarcinoma cells showed impaired tumor progression, angiogenesis and metastasis to the lung, compared with wildtype littermate controls. These mutant mice may be useful in studies of postnatal angiogenesis (endothelial cell migration, assembly into new tubules, and cytoskeletal regulation), or as a tool to study cancer, especially breast cancer research.Development
A targeting vector containing the neomycin cassette was used to disrupt exon 5 (at nucleotide 1372, corresponding to amino acid residue 426 in the extracellular domain) of the endogenous Epha2 gene. This construct was microinjected into 129S6/SvEvTac-derived CCE embryonic stem (ES) cells. Correctly targeted ES cells were injected into C57BL/6 blastocysts. Resulting chimeric males were bred to C57BL/6 females for one generation and backcrossed to BALB/c once before being interbred to homozygosity. Mutant null mice were maintained by sibling matings for more than 10 years prior to arrival at The Jackson Laboratory. The mice were then backcrossed on to the BALB/cByJ (Stock No. 001026) background for 5 generations.
| Control | ||
|---|---|---|
| 001026 BALB/cByJ | ||
| Considerations for Choosing Controls | ||
Strains carrying Epha2tm1Jrui allele
006028 B6;129S6-Epha2tm1Jrui/J View Strains carrying Epha2tm1Jrui (1 strain)
View Related Disease (OMIM) Terms
Related Disease (OMIM) Terms provided by MGI
- Potential model based on gene homology relationships. Phenotypic similarity to the human disease has not been tested. Cataract 6, Multiple Types; CTRCT6 (EPHA2)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms provided by MGI
assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Epha2tm1Jrui/Epha2tm1Jrui
involves: 129 * BALB/c * C57BL/6View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Cancer Research
Other
tumor metastasis
Tumor Resistance
Tumor Suppressor Genes
Cardiovascular Research
Vascular Defects
Research Tools
Cancer Research
anti-tumor activity
tumor immunology
Cardiovascular Research
| Allele Symbol | Epha2tm1Jrui | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Joseph C Ruiz | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | Epha2-; Epha2tm1Jinc; | ||
| Mutation Made By | Joseph Ruiz, Indiana University School of Medicine | ||
| Gene Symbol and Name | Epha2, Eph receptor A2 | ||
| Chromosome | 4 | ||
| Gene Common Name(s) | ARCC2; AW545284; CTPA; CTPP1; CTRCT6; ECK; Eck; Myk2; Sek-2; Sek2; epithelial cell kinase; expressed sequence AW545284; | ||
| Molecular Note | A neo cassette was inserted at nucleotide 1372, within the sequence encoding the extracellular domain. Although the resultant transcript putatively encodes a nonfunctional protein truncated at amino acid 426, no protein was detected by Western blot analysis of murine pulmonary microvascular endothelial cells from mutant mice. [MGI Ref ID J:89275] | ||
Genotyping Protocols
Epha2tm1Jrui, Separated PCR
Helpful Links
Genotyping resources and troubleshooting
Brantley-Sieders DM; Caughron J; Hicks D; Pozzi A; Ruiz JC; Chen J. 2004. EphA2 receptor tyrosine kinase regulates endothelial cell migration and vascular assembly through phosphoinositide 3-kinase-mediated Rac1 GTPase activation. J Cell Sci 117(Pt 10):2037-49. [PubMed: 15054110] [MGI Ref ID J:89275]
Epha2tm1Jrui relatedBrantley-Sieders DM; Fang WB; Hicks DJ; Zhuang G; Shyr Y; Chen J. 2005. Impaired tumor microenvironment in EphA2-deficient mice inhibits tumor angiogenesis and metastatic progression. FASEB J 19(13):1884-6. [PubMed: 16166198] [MGI Ref ID J:102664]
Brantley-Sieders DM; Zhuang G; Hicks D; Fang WB; Hwang Y; Cates JM; Coffman K; Jackson D; Bruckheimer E; Muraoka-Cook RS; Chen J. 2008. The receptor tyrosine kinase EphA2 promotes mammary adenocarcinoma tumorigenesis and metastatic progression in mice by amplifying ErbB2 signaling. J Clin Invest 118(1):64-78. [PubMed: 18079969] [MGI Ref ID J:130805]
Carpenter TC; Schroeder W; Stenmark KR; Schmidt EP. 2012. Eph-A2 promotes permeability and inflammatory responses to bleomycin-induced lung injury. Am J Respir Cell Mol Biol 46(1):40-7. [PubMed: 21799118] [MGI Ref ID J:191913]
Hahn AS; Kaufmann JK; Wies E; Naschberger E; Panteleev-Ivlev J; Schmidt K; Holzer A; Schmidt M; Chen J; Konig S; Ensser A; Myoung J; Brockmeyer NH; Sturzl M; Fleckenstein B; Neipel F. 2012. The ephrin receptor tyrosine kinase A2 is a cellular receptor for Kaposi's sarcoma-associated herpesvirus. Nat Med 18(6):961-6. [PubMed: 22635007] [MGI Ref ID J:186781]
Okazaki T; Ni A; Baluk P; Ayeni OA; Kearley J; Coyle AJ; Humbles A; McDonald DM. 2009. Capillary defects and exaggerated inflammatory response in the airways of EphA2-deficient mice. Am J Pathol 174(6):2388-99. [PubMed: 19443703] [MGI Ref ID J:148922]
Rao A; Taylor JL; Chi-Sabins N; Kawabe M; Gooding WE; Storkus WJ. 2012. Combination therapy with HSP90 inhibitor 17-DMAG reconditions the tumor microenvironment to improve recruitment of therapeutic T cells. Cancer Res 72(13):3196-206. [PubMed: 22552283] [MGI Ref ID J:189322]
Shi Y; De Maria A; Bennett T; Shiels A; Bassnett S. 2012. A role for epha2 in cell migration and refractive organization of the ocular lens. Invest Ophthalmol Vis Sci 53(2):551-9. [PubMed: 22167091] [MGI Ref ID J:191524]
Vaught D; Chen J; Brantley-Sieders DM. 2009. Regulation of mammary gland branching morphogenesis by EphA2 receptor tyrosine kinase. Mol Biol Cell 20(10):2572-81. [PubMed: 19321667] [MGI Ref ID J:175142]
Animal Health Reports
Production of mice from cryopreserved embryos or sperm occurs in a maximum barrier room, G200.Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice are bred as homozygotes.
| Pricing for USA, Canada and Mexico shipping destinations |
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Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $2450.00 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 on the strain data sheet for further information.
Supply Notes
Cryorecovery - Standard.
Progeny testing is not required.
The average number of mice provided from recovery of our cryopreserved strains is 10. The total number of animals provided, their gender and genotype will vary. We will fulfill your order by providing at least two pair of mice, at least one animal of each pair carrying the mutation of interest. Please inquire if larger numbers of animals with specific genotype and genders are needed. Animals typically ship between 11 and 14 weeks from the date of your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will ship within 25 weeks. IMPORTANT NOTE: The genotypes of animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire about possible genotypes which will be recovered for this specific strain. The Jackson Laboratory cannot guarantee the reproductive success of mice shipped to your facility. If the mice are lost after the first three days (post-arrival) or do not produce progeny at your facility, a new order and fee will be necessary.Cryorecovery to establish a Dedicated Supply for greater quantities of mice
Mice recovered can be used to establish a dedicated colony to contractually supply you mice according to your requirements. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 (from U.S.A., Canada or Puerto Rico only) or 1-207-288-5845 (from any location).
| Pricing for International shipping destinations |
|
Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $3185.00 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 on the strain data sheet for further information.
Supply Notes
Cryorecovery - Standard.
Progeny testing is not required.
The average number of mice provided from recovery of our cryopreserved strains is 10. The total number of animals provided, their gender and genotype will vary. We will fulfill your order by providing at least two pair of mice, at least one animal of each pair carrying the mutation of interest. Please inquire if larger numbers of animals with specific genotype and genders are needed. Animals typically ship between 11 and 14 weeks from the date of your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will ship within 25 weeks. IMPORTANT NOTE: The genotypes of animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire about possible genotypes which will be recovered for this specific strain. The Jackson Laboratory cannot guarantee the reproductive success of mice shipped to your facility. If the mice are lost after the first three days (post-arrival) or do not produce progeny at your facility, a new order and fee will be necessary.Cryorecovery to establish a Dedicated Supply for greater quantities of mice
Mice recovered can be used to establish a dedicated colony to contractually supply you mice according to your requirements. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 (from U.S.A., Canada or Puerto Rico only) or 1-207-288-5845 (from any location).
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Cryopreserved. Ready for recovery. Please refer to pricing and supply notes on the strain data sheet for further information.
| Control | ||
|---|---|---|
| 001026 BALB/cByJ | ||
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
For Licensing and Use Restrictions view the link(s) below:
- Use of MICE by companies or for-profit entities requires a license prior to shipping.
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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