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Former Names B6;129X1-Grprtm1Jfb/J (Changed: 30-NOV-05 ) Type Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Donating Investigator Dr. Lori Hampton, NIDCD-NIH Appearance
black
Related Genotype: a/aDescription
Mice homozygous (females) or hemizygous (males) for the X-linked Grprtm1Jfb targeted mutation are viable with no gross phenotypic abnormalities observed. There is a deficiency in bombesin-induced mediation of satiety as measured by glucose intake. A modest increase in body weight is observed in older animals. At 18-20 months of age, hemizygous males (N = 8) are 44.5g ± 5.1 (mean ± std dev) and wildtype littermates (N = 8) are 38.3g ± 5.1 (L. Hampton, unpublished observation). We have recently observed head tilts and bobbing in the hemizygous males in our production colony. The donating investigator of this strain has also observed this phenotype and considers it a mutation not related to the gene. We are working to remove this phenotype, but we will continue to ship from the colony while we finish this process.Development
A targeting vector containing neomycin resistance and herpes simplex virus thymidine kinase genes was used to disrupt exon 1. The construct was electroporated into 129X1/SvJ derived RW-4 embryonic stem (ES) cells. Correctly targeted ES cells were injected into recipient blastocysts. The resulting chimeric animals were crossed to C57BL/6J mice, and then backcrossed to the same for 8 generations.
| Control | ||
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| 000664 C57BL/6J | ||
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View Mammalian Phenotype Terms
Mammalian Phenotype Terms provided by MGI
assigned by genotype
Grprtm1Jfb/Grprtm1Jfb
involves: 129X1/SvJ * C57BL/6J
- normal phenotype
- no abnormal phenotype detected
- female homozygotes are viable, fertile and developmentally normal with no pathological or histological abnormalities in all major organ systems up to 10 months of age (MGI Ref ID J:46897)
Grprtm1Jfb/Y
involves: 129X1/SvJ * C57BL/6J
- behavior/neurological phenotype
- abnormal food intake
- male hemizygotes are viable, fertile and developmentally normal with no pathological or histological abnormalities in all major organ systems up to 10 months of age (MGI Ref ID J:46897)
- however, male hemizygotes lack a bombesin (BN)-induced satiety response: BN produces a significant suppression of glucose intake in wild-type mice at doses of 3.2, 10, and 32 nmol/kg but fails to suppress glucose intake at any dose with no apparent weight gain in mutant males (MGI Ref ID J:46897)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Grprtm1Jfb related
Cancer Research
Genes Regulating Growth and Proliferation
Growth Factors/Receptors/Cytokines
Diabetes and Obesity Research
Obesity Without Diabetes
moderate, adult onset
Endocrine Deficiency Research
Gastrointestinal Defects
Pancreas Defects
Neurobiology Research
Behavioral and Learning Defects
Metabolic Defects
| Allele Symbol | Grprtm1Jfb | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, James F Battey | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | GRP-R-; GRPR-; | ||
| Mutation Made By | Dr. Lori Hampton, NIDCD-NIH | ||
| Strain of Origin | 129X1/SvJ | ||
| ES Cell Line Name | RW-4 | ||
| ES Cell Line Strain | 129X1/SvJ | ||
| Gene Symbol and Name | Grpr, gastrin releasing peptide receptor | ||
| Chromosome | X | ||
| Gene Common Name(s) | GRP-R; bombesin receptor; | ||
| Molecular Note | A neomycin resistance cassette disrupted exon 1 of the gene. [MGI Ref ID J:46897] | ||
Genotyping Protocols
Grprtm1Jfb,Separated MCA
Grprtm1Jfb, Separated PCR
Helpful Links
Genotyping resources and troubleshooting
Hampton LL; Ladenheim EE; Akeson M; Way JM; Weber HC; Sutliff VE ; Jensen RT ; Wine LJ ; Arnheiter H ; Battey JF. 1998. Loss of bombesin-induced feeding suppression in gastrin-releasing peptide receptor-deficient mice. Proc Natl Acad Sci U S A 95(6):3188-92. [PubMed: 9501238] [MGI Ref ID J:46897]
Hampton LL; Wright CG; Alagramam KN; Battey JF; Noben-Trauth K. 2003. A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15. Hear Res 180(1-2):67-75. [PubMed: 12782354] [MGI Ref ID J:84779]
Ladenheim EE; Hampton LL; Whitney AC; White WO; Battey JF; Moran TH. 2002. Disruptions in feeding and body weight control in gastrin-releasing peptide receptor deficient mice. J Endocrinol 174(2):273-81. [PubMed: 12176666] [MGI Ref ID J:78753]
Grprtm1Jfb relatedBalci F; Papachristos EB; Gallistel CR; Brunner D; Gibson J; Shumyatsky GP. 2008. Interval timing in genetically modified mice: a simple paradigm. Genes Brain Behav 7(3):373-84. [PubMed: 17696995] [MGI Ref ID J:147479]
Carroll RE; Matkowskyj K; Saunthararajah Y; Sekosan M; Battey JF; Benya RV. 2002. Contribution of gastrin-releasing peptide and its receptor to villus development in the murine and human gastrointestinal tract. Mech Dev 113(2):121-30. [PubMed: 11960700] [MGI Ref ID J:76548]
Carroll RE; Matkowskyj KA; Tretiakova MS; Battey JF; Benya RV. 2000. Gastrin-releasing peptide is a mitogen and a morphogen in murine colon cancer Cell Growth Differ 11(7):385-93. [PubMed: 10939592] [MGI Ref ID J:63661]
Chaperon F; Fendt M; Kelly PH; Lingenhoehl K; Mosbacher J; Olpe HR; Schmid P; Sturchler C; McAllister KH; van der Putten PH; Gee CE. 2012. Gastrin-releasing peptide signaling plays a limited and subtle role in amygdala physiology and aversive memory. PLoS One 7(4):e34963. [PubMed: 22509372] [MGI Ref ID J:187094]
Ladenheim EE; Hampton LL; Whitney AC; White WO; Battey JF; Moran TH. 2002. Disruptions in feeding and body weight control in gastrin-releasing peptide receptor deficient mice. J Endocrinol 174(2):273-81. [PubMed: 12176666] [MGI Ref ID J:78753]
Lagerstrom MC; Rogoz K; Abrahamsen B; Persson E; Reinius B; Nordenankar K; Olund C; Smith C; Mendez JA; Chen ZF; Wood JN; Wallen-Mackenzie A; Kullander K. 2010. VGLUT2-dependent sensory neurons in the TRPV1 population regulate pain and itch. Neuron 68(3):529-42. [PubMed: 21040852] [MGI Ref ID J:167752]
Liu XY; Liu ZC; Sun YG; Ross M; Kim S; Tsai FF; Li QF; Jeffry J; Kim JY; Loh HH; Chen ZF. 2011. Unidirectional Cross-Activation of GRPR by MOR1D Uncouples Itch and Analgesia Induced by Opioids. Cell 147(2):447-58. [PubMed: 22000021] [MGI Ref ID J:177501]
Martel G; Hevi C; Wong A; Zushida K; Uchida S; Shumyatsky GP. 2012. Murine GRPR and stathmin control in opposite directions both cued fear extinction and neural activities of the amygdala and prefrontal cortex. PLoS One 7(2):e30942. [PubMed: 22312434] [MGI Ref ID J:185238]
Shumyatsky GP; Tsvetkov E; Malleret G; Vronskaya S; Hatton M; Hampton L; Battey JF; Dulac C; Kandel ER; Bolshakov VY. 2002. Identification of a signaling network in lateral nucleus of amygdala important for inhibiting memory specifically related to learned fear. Cell 111(6):905-18. [PubMed: 12526815] [MGI Ref ID J:80849]
Sun YG; Chen ZF. 2007. A gastrin-releasing peptide receptor mediates the itch sensation in the spinal cord. Nature 448(7154):700-3. [PubMed: 17653196] [MGI Ref ID J:123810]
Sun YG; Zhao ZQ; Meng XL; Yin J; Liu XY; Chen ZF. 2009. Cellular basis of itch sensation. Science 325(5947):1531-4. [PubMed: 19661382] [MGI Ref ID J:152477]
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 by crossing heterozygous or homozygous females and hemizygous males. This is a targeted mutation of an X-linked gene. Expected coat color from breeding: Black. Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
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Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $1980.00 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* $2574.00 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 | ||
|---|---|---|
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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