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Type Transgenic; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Generation N?pN1
Generation DefinitionsDonating Investigator Jamey D Marth, Burnham Inst at Univ Calif Santa Barbara Description
This is a transgenic line in which Cre recombinase expression is controlled by the regulatory sequences from the mouse zona pellucida 3 (Zp3) gene, which is normally expressed exclusively in the growing oocyte prior to the completion of the first meiotic division. This strain is useful for deleting a loxP-flanked genomic segment during oogenesis and thereby producing embryos and offspring that bear the recombined and deleted genomic element(s).Development
The ZP3-Cre transgene was constructed by linking the Zp3 promoter to the Cre gene as well as the human growth hormone splicing and polyadenylation signals.
Strains carrying other alleles of Zp3
004038 B6.129S4-Zp3tm1Dean/J 003394 B6.FVB-Tg(Zp3-cre)3Mrt/J 003651 C57BL/6-Tg(Zp3-cre)93Knw/J 003650 C57BL/6J-Tg(Zp3-cre)82Knw/KnwJ 003377 FVB/N-Tg(Zp3-cre)3Mrt/J 006129 STOCK Tg(Zp3-EGFP)1Dean/J View Strains carrying other alleles of Zp3 (6 strains)
Strains carrying other alleles of cre
View Strains carrying other alleles of cre (394 strains)
Introduction to Cre-lox technology
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
cre relatedResearch Tools
Cre-lox System
Cre Recombinase Expression
Cre Recombinase Expression: Germline/Embryonic Expression
Research Tools
Cre-lox System
Genetics Research
Mutagenesis and Transgenesis
Mutagenesis and Transgenesis: Cre-lox System
| Allele Symbol | Tg(Zp3-cre)1Gwh | ||
|---|---|---|---|
| Allele Name | transgene insertion 1, Gerald W Hart | ||
| Allele Type | Transgenic (Cre/Flp) | ||
| Common Name(s) | ZP3-Cre; ZP3Cre; | ||
| Mutation Made By | Jamey Marth, Burnham Inst at Univ Calif Santa Barbara | ||
| Site of Expression | cre recombinase is expressed in oocytes. | ||
| Expressed Gene | cre, cre recombinase, bacteriophage P1 | ||
| Cre recombinase is an enzyme derived from the bacteriophage P1 that specifically recognizes loxP sites. Cre has been shown to effectively mediate the excision of DNA located between loxP sites. After the excision event, the DNA ends recombine leaving a single loxP site in place of the intervening sequence. | |||
| Promoter | Zp3, zona pellucida glycoprotein 3, mouse, laboratory | ||
| Gene Symbol and Name | Tg(Zp3-cre)1Gwh, transgene insertion 1, Gerald W Hart | ||
| Chromosome | UN | ||
| Gene Common Name(s) | ZP3-Cre; ZP3Cre; | ||
| Driver Note | Zp3 | ||
| Molecular Note | A 6 kb fragment encompassing the promoter sequence of Zp3 was adjoined to the cre recombinase coding region and human growth hormone splicing and polyadenylation signals. The Zp3 promoter region was reported to direct expression in oocytes. [MGI Ref ID J:102175] [MGI Ref ID J:62279] | ||
Genotyping Protocols
Tg(Zp3-cre)1Gwh, Standard PCR
Helpful Links
Genotyping resources and troubleshooting
Shafi R; Iyer SP; Ellies LG; O'Donnell N; Marek KW; Chui D; Hart GW; Marth JD. 2000. The O-GlcNAc transferase gene resides on the X chromosome and is essential for embryonic stem cell viability and mouse ontogeny. Proc Natl Acad Sci U S A 97(11):5735-9. [PubMed: 10801981] [MGI Ref ID J:62279]
Tg(Zp3-cre)1Gwh relatedAlfieri JA; Martin AD; Takeda J; Kondoh G; Myles DG; Primakoff P. 2003. Infertility in female mice with an oocyte-specific knockout of GPI-anchored proteins. J Cell Sci 116(Pt 11):2149-55. [PubMed: 12692150] [MGI Ref ID J:83792]
Ge C; Liu T; Hou X; Stanley P. 2008. In vivo consequences of deleting EGF repeats 8-12 including the ligand binding domain of mouse Notch1. BMC Dev Biol 8:48. [PubMed: 18445292] [MGI Ref ID J:136658]
Grasa P; Kaune H; Williams SA. 2012. Embryos generated from oocytes lacking complex N- and O-glycans have compromised development and implantation. Reproduction 144(4):455-65. [PubMed: 22919046] [MGI Ref ID J:191575]
He ZY; Brakebusch C; Fassler R; Kreidberg JA; Primakoff P; Myles DG. 2003. None of the integrins known to be present on the mouse egg or to be ADAM receptors are essential for sperm-egg binding and fusion. Dev Biol 254(2):226-37. [PubMed: 12591243] [MGI Ref ID J:82124]
O'Donnell N; Zachara NE; Hart GW; Marth JD. 2004. Ogt-dependent X-chromosome-linked protein glycosylation is a requisite modification in somatic cell function and embryo viability. Mol Cell Biol 24(4):1680-90. [PubMed: 14749383] [MGI Ref ID J:93112]
Ohtsubo K; Takamatsu S; Minowa MT; Yoshida A; Takeuchi M; Marth JD. 2005. Dietary and genetic control of glucose transporter 2 glycosylation promotes insulin secretion in suppressing diabetes. Cell 123(7):1307-21. [PubMed: 16377570] [MGI Ref ID J:117542]
Pospichalova V; Tureckova J; Fafilek B; Vojtechova M; Krausova M; Lukas J; Sloncova E; Takacova S; Divoky V; Leprince D; Plachy J; Korinek V. 2011. Generation of two modified mouse alleles of the Hic1 tumor suppressor gene. Genesis 49(3):142-51. [PubMed: 21309068] [MGI Ref ID J:170337]
Schmid RS; Tsujimoto N; Qu Q; Lei H; Li E; Chen T; Blaustein CS. 2008. A methyl-CpG-binding protein 2-enhanced green fluorescent protein reporter mouse model provides a new tool for studying the neuronal basis of Rett syndrome. Neuroreport 19(4):393-8. [PubMed: 18287934] [MGI Ref ID J:136605]
Shi S; Stahl M; Lu L; Stanley P. 2005. Canonical Notch signaling is dispensable for early cell fate specifications in mammals. Mol Cell Biol 25(21):9503-8. [PubMed: 16227600] [MGI Ref ID J:102175]
Shi S; Williams SA; Seppo A; Kurniawan H; Chen W; Ye Z; Marth JD; Stanley P. 2004. Inactivation of the Mgat1 gene in oocytes impairs oogenesis, but embryos lacking complex and hybrid N-glycans develop and implant. Mol Cell Biol 24(22):9920-9. [PubMed: 15509794] [MGI Ref ID J:94224]
Stahl M; Ge C; Shi S; Pestell RG; Stanley P. 2006. Notch1-induced transformation of RKE-1 cells requires up-regulation of cyclin D1. Cancer Res 66(15):7562-70. [PubMed: 16885355] [MGI Ref ID J:112097]
Tenno M; Ohtsubo K; Hagen FK; Ditto D; Zarbock A; Schaerli P; von Andrian UH; Ley K; Le D; Tabak LA; Marth JD. 2007. Initiation of protein O glycosylation by the polypeptide GalNAcT-1 in vascular biology and humoral immunity. Mol Cell Biol 27(24):8783-96. [PubMed: 17923703] [MGI Ref ID J:128982]
Williams SA; Stanley P. 2009. Complex N-glycans or core 1-derived O-glycans are not required for the expression of stage-specific antigens SSEA-1, SSEA-3, SSEA-4, or Le(Y) in the preimplantation mouse embryo. Glycoconj J 26(3):335-47. [PubMed: 18773292] [MGI Ref ID J:146690]
Williams SA; Stanley P. 2009. Oocyte-specific deletion of complex and hybrid N-glycans leads to defects in preovulatory follicle and cumulus mass development. Reproduction 137(2):321-31. [PubMed: 19028923] [MGI Ref ID J:150225]
Williams SA; Xia L; Cummings RD; McEver RP; Stanley P. 2007. Fertilization in mouse does not require terminal galactose or N-acetylglucosamine on the zona pellucida glycans. J Cell Sci 120(Pt 8):1341-9. [PubMed: 17374637] [MGI Ref ID J:122012]
Animal Health Reports
Production of mice from cryopreserved embryos or sperm occurs in a maximum barrier room, G200.
| 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.
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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