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| These Tiparp-mutant mice may be useful in studying cellular signaling in development and adult mice; specifically receptor tyrosine kinases (RTK; such as Ras, MAP kinase, PI3K and those in the platelet-derived growth factor (PDGF) family) and immediate early genes (IEG) induced shortly after RTK activation. Homozygotes occur at lower than Mendelian ratio (22%), and 32% die by age 2 week. Homozygotes exhibit abnormalities in vascular and kidney development, anemia, polychromasia and abnormalities in palate bone fusion. | |||||||||
Type Gene Trap; Mutant Stock; Additional information on Genetically Engineered Mutant Mice. Mating System Heterozygote x Heterozygote (Female x Male) Species laboratory mouse Generation ?+F3 (13-OCT-08) Donating Investigator Philippe Soriano, Mount Sinai School of Medicine Description
Homozygous embryos E11.5 to E18.5 exhibit hemorrhages and microaneurisms. Vascular defects persist into adulthood. At 6 weeks of age, mice are anemic (low hemoglobin concentration, red blood cell count, hematocrit). These mice also exhibit polychromasia (abnormally high number of immature blood cells); kidney defects (blood urea nitrogen level abnormally high, kidney size smaller than wildtype, swollen blood filled, degraded glomeruli are often observed, increased number of vascular smooth muscle cells partially filling the glomeruli space); and abnormalities in palate bone fusion. Homozygotes occur at lower than Mendelian ratio (22%), and 32% die by age 2 week. Heterozygotes are viable and fertile. No gene product is detected in homozygous embryos aged ED9.5-12.5 or in adult gonad. These Tiparp-mutant mice may be useful in studying kidney development, vascular development, hematopoiesis and cellular signaling during development and in adult mice; specifically receptor tyrosine kinases (RTK; such as Ras, MAP kinase, PI3K and those in the platelet-derived growth factor (PDGF) family) and immediate early genes (IEG) induced shortly after RTK activation.Development
The retroviral gene-trap vector ROSAFARY (or reverse orientation splice acceptor for array) was designed with a promoter trap module (SAβgeo*pA; encoding a lacZ-neo fusion gene) and an frt-flanked poly-A trap module (PGKhygSD; PGK promoter-driven hygromycin gene with adenoviral splice donor). This construct was electroporated into 129S4/SvJaeSor-derived AK7.1 embryonic stem (ES) cells. ES cells with the ROSAFARY vector correctly targeted to the Tiparp gene (in the 1st intron) were identified and used to generate mutant mice. These mutant mice were maintained on a mixed B6;129S4 background prior to arrival at The Jackson Laboratory. The mice were then crossed to C57BL/6J (Stock No. 000664) for one generation.The ROSAFARY vector inserts a promoterless lacZ-neo reporter fusion gene (which functions as an artificial 3' terminal exon to intercept and terminate transcription from the targeted gene promoter) as well as a poly-A trap (which functions as an artificial 5' terminal exon to initiate transcription from the insertion site). After inserting into an intron of an endogenous gene at a permissive site and in the correct orientation, the promoter trap module and the poly-A trap module can be activated to form fusion transcripts with the 5' or 3' exons.
| Control | ||
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| Wild-type from the colony | ||
| Considerations for Choosing Controls | ||
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
involves: 129S4/SvJaeSor
- lethality-postnatal
- postnatal lethality (MGI Ref ID J:117491)
- 32% of mice die by week 2
- skeleton phenotype
- abnormal skeleton morphology (MGI Ref ID J:117491)
- abnormal neural crest derived and thoracic skeleton
- abnormal calvaria morphology (MGI Ref ID J:117491)
- 55% of mice have reduced calvarial bones at the midline with increases in the gaps between frontal bones
- abnormal frontal bone morphology (MGI Ref ID J:117491)
- increases in the gaps between frontal bones
- abnormal palatine shelf (MGI Ref ID J:117491)
- 78% of mice have smaller and less extended towards the midline palatine and presphenoid bones
- abnormal presphenoid bone morphology (MGI Ref ID J:117491)
- 78% of mice have smaller and less extended towards the midline palatine and presphenoid bones
- abnormal sternum morphology (MGI Ref ID J:117491)
- 44% of mice have sternum defects including asymmetric or additional fusion of ribs and gaps in the sternum
- asymmetric rib-sternum attachment (MGI Ref ID J:117491)
- short maxilla (MGI Ref ID J:117491)
- short nasal bone (MGI Ref ID J:117491)
- short premaxilla (MGI Ref ID J:117491)
- renal/urinary system phenotype
- abnormal kidney morphology (MGI Ref ID J:117491)
- abnormal renal glomerulus morphology (MGI Ref ID J:117491)
- glomeruli are often degraded
- excess smooth muscle cells are found in the glomeruli
- pale kidney (MGI Ref ID J:117491)
- small kidney (MGI Ref ID J:117491)
- kidney inflammation (MGI Ref ID J:117491)
- kidney is swollen in sections and blood filled
- hematopoietic system phenotype
- abnormal red blood cell (MGI Ref ID J:117491)
- an increase in immature red blood cells is observed compared to wild-type mice
- anemia (MGI Ref ID J:117491)
- by week 6
- decreased erythrocyte cell number (MGI Ref ID J:117491)
- by week 6
- decreased hematocrit (MGI Ref ID J:117491)
- by week 6
- decreased hemoglobin content (MGI Ref ID J:117491)
- by week 6
- polychromatophilia (MGI Ref ID J:117491)
- homeostasis/metabolism phenotype
- increased blood urea nitrogen level (MGI Ref ID J:117491)
- cardiovascular system phenotype
- abnormal vasculature (MGI Ref ID J:117491)
- hemorrhage (MGI Ref ID J:117491)
- at E11.5-E18.5
- muscle phenotype
- abnormal smooth muscle morphology (MGI Ref ID J:117491)
- excess smooth muscle cells are found in the glomeruli
- immune system phenotype
- kidney inflammation (MGI Ref ID J:117491)
- kidney is swollen in sections and blood filled
- craniofacial phenotype
- abnormal calvaria morphology (MGI Ref ID J:117491)
- 55% of mice have reduced calvarial bones at the midline with increases in the gaps between frontal bones
- abnormal frontal bone morphology (MGI Ref ID J:117491)
- increases in the gaps between frontal bones
- abnormal palate morphology (MGI Ref ID J:117491)
- irregularities in fusion persist into adulthood
- abnormal palatine shelf (MGI Ref ID J:117491)
- 78% of mice have smaller and less extended towards the midline palatine and presphenoid bones
- abnormal presphenoid bone morphology (MGI Ref ID J:117491)
- 78% of mice have smaller and less extended towards the midline palatine and presphenoid bones
- abnormal snout morphology (MGI Ref ID J:117491)
- shorter and wider than in wild-type mice
- short maxilla (MGI Ref ID J:117491)
- short nasal bone (MGI Ref ID J:117491)
- short premaxilla (MGI Ref ID J:117491)
- digestive/alimentary phenotype
- abnormal palate morphology (MGI Ref ID J:117491)
- irregularities in fusion persist into adulthood
- abnormal palatine shelf (MGI Ref ID J:117491)
- 78% of mice have smaller and less extended towards the midline palatine and presphenoid bones
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Cardiovascular Research
Vascular Defects
Cell Biology Research
Signal Transduction
Developmental Biology Research
Craniofacial and Palate Defects
Embryonic Lethality (Homozygous) (incomplete)
Internal/Organ Defects (kidney)
Perinatal Lethality (Homozygous)
Hematological Research
Hematopoietic Defects
| Allele Symbol | TiparpGt(ROSA)79Sor | ||
|---|---|---|---|
| Allele Name | gene trapped 79, Philippe M Soriano | ||
| Allele Type | Gene trapped | ||
| Common Name(s) | Tiparp-; | ||
| Mutation Made By | Philippe Soriano, Fred Hutchinson Cancer Research Center | ||
| Strain of Origin | 129S4/SvJaeSor | ||
| ES Cell Line Name | AK7 | ||
| ES Cell Line Strain | 129S4/SvJaeSor | ||
| Gene Symbol and Name | Tiparp, TCDD-inducible poly(ADP-ribose) polymerase | ||
| Chromosome | 3 | ||
| Gene Common Name(s) | AW558171; DDF1; DKFZp434J214; DKFZp686N0351; DKFZp686P1838; FLJ40466; PARP-1; PARP-7; PARP7; expressed sequence AW558171; | ||
| Molecular Note | The Rosafary gene trap vector containing a SAbetaGeo pA promoter trap module and a PGKhygSD poly-A trap module was inserted into intron 1. [MGI Ref ID J:117491] | ||
Genotyping Protocols
TiparpGt(ROSA)79Sor, SEP PCR, vers. 1
Helpful Links
Optimizing PCR Protocols
Schmahl J; Raymond CS; Soriano P. 2007. PDGF signaling specificity is mediated through multiple immediate early genes. Nat Genet 39(1):52-60. [PubMed: 17143286] [MGI Ref ID J:117491]
Animal Health Reports
Room Number AX12
Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice can be bred as heterozygotes. Homozygotes occur at lower than Mendelian ratio (22%), and 32% die by age 2 week. The Donating Investigator used a breeding scheme of homozygous male x heterozygous female. Mating System Heterozygote x Heterozygote (Female x Male) Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
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Weeks of Age Price* Gender Genotypes Provided Individual Mouse Price $236.40 Female or Male Heterozygous for TiparpGt(ROSA)79Sor *Price(s) in US dollars ($)
Pairs /Price* Pair Genotype $288.90 Heterozygous for TiparpGt(ROSA)79Sor x Wildtype for TiparpGt(ROSA)79Sor $288.90 Wildtype for TiparpGt(ROSA)79Sor x Heterozygous for TiparpGt(ROSA)79Sor
| Supply Notes |
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| Pricing for International shipping destinations |
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Weeks of Age Price* Gender Genotypes Provided Individual Mouse Price $307.40 Female or Male Heterozygous for TiparpGt(ROSA)79Sor *Price(s) in US dollars ($)
Pairs /Price* Pair Genotype $375.60 Heterozygous for TiparpGt(ROSA)79Sor x Wildtype for TiparpGt(ROSA)79Sor $375.60 Wildtype for TiparpGt(ROSA)79Sor x Heterozygous for TiparpGt(ROSA)79Sor
| Supply Notes |
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| 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. |
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| Supply Notes |
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| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
Purchasing Information
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| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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