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| These Sufu, suppressor of fused homolog (Drosophila), mutant mice may be useful in studying the Hedgehog signaling pathway and embryonic development. Homozygotes for the allele fail to develop past embryonic day 10 and exhibit growth retardation, incomplete embryonic turning, abnormal somite development, abnormal left-right axial patterning and open neural tubes. | |||||||||
Type Coisogenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered Mutant Mice. Mating System +/+ sibling x Heterozygote (Female x Male) Species laboratory mouse Generation ?+F2 (09-OCT-08) Donating Investigator Allen Bale, Yale University Description
Mice that are heterozygous for the targeted mutation are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities. Homozygous null mice have an embryonic lethal phenotype, failing to develop past embryonic days 9.5 to 10. No gene product (protein) is detected by Western blot analysis. Truncated gene product (mRNA) is detected by Northern blot analysis. Homozygous embryos at 9 to 9.5 embryonic day exhibit growth retardation, incomplete embryonic turning, abnormal somite development, abnormal heart looping (due to abnormal left-right axial patterning) and open neural tubes. This mutant mouse strain may be useful in studies of the Hedgehog signaling pathway and embryonic development.Development
A targeting vector containing a loxP site flanked (floxed) neomycin resistance and herpes simplex virus thymidine kinase genes was used to disrupt the intron 6/exon 7 junction and part of exon 7. The construct was electroporated into 129S1/Sv-p+ Tyr+ Kitl+ derived W9.5 embryonic stem (ES) cells. Correctly targeted ES cells were injected into C57BL/6 blastocysts. The resulting chimeric male animals were crossed to 129S1 female mice. The strain was maintained as heterozygotes on the 129S1 background prior to arriving at The Jackson Laboratory.
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 002448 129S1/SvImJ | (approximate) | |
| Considerations for Choosing Controls | ||
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Sufutm1Aeb/Sufu+
either: 129S1/Sv-Sufutm1Aeb or (involves: 129S1/Sv * C57BL/6)
- normal phenotype
- no abnormal phenotype detected (MGI Ref ID J:101731)
- exhibit no obvious abnormalities, internal malformations or tumor predisposition
Sufutm1Aeb/Sufutm1Aeb
either: 129S1/Sv-Sufutm1Aeb or (involves: 129S1/Sv * C57BL/6)
- lethality-prenatal/perinatal
- embryonic lethality during organogenesis (MGI Ref ID J:101731)
- do not survive past E10.5
- embryogenesis phenotype
- abnormal developmental patterning (MGI Ref ID J:101731)
- abnormal dorsal-ventral axis patterning (MGI Ref ID J:101731)
- abnormal left-right axis patterning (MGI Ref ID J:101731)
- abnormal heart looping indicates abnormal development of left-right asymmetry
- abnormal primitive streak morphology (MGI Ref ID J:101731)
- abnormal node architecture at E7.75, ranging from mild changes in the shape of the node to irregular distribution of nodal cells
- incomplete embryo turning (MGI Ref ID J:101731)
- by E9-9.5, fail to undergo embryo turning
- abnormal somite development (MGI Ref ID J:101731)
- observed by E9-9.5
- embryonic growth retardation (MGI Ref ID J:101731)
- embryonic growth retardation is observed by E9-9.5 but not at E8.5
- nervous system phenotype
- open neural tube (MGI Ref ID J:101731)
- cardiovascular system phenotype
- abnormal aorta morphology (MGI Ref ID J:101731)
- descending aorta is dilated
- abnormal cardiac muscle morphology (MGI Ref ID J:101731)
- myocardium hyperplasia
- abnormal direction of looping morphogenesis (MGI Ref ID J:101731)
- 4 of 13 have L-looped (leftward) hearts at E9.5-10.5 and one has indeterminate cardiac looping
- aneurysm (MGI Ref ID J:101731)
- 4 of 14 have aneurysms in the diencephalic hemispheres
- hemorrhage (MGI Ref ID J:101731)
- 4 of 14 have hemorrhage in the diencephalic hemispheres
- muscle phenotype
- abnormal cardiac muscle morphology (MGI Ref ID J:101731)
- myocardium hyperplasia
- growth/size phenotype
- embryonic growth retardation (MGI Ref ID J:101731)
- embryonic growth retardation is observed by E9-9.5 but not at E8.5
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Developmental Biology Research
Embryonic Lethality (Homozygous)
Growth Defects
Internal/Organ Defects (heart)
Neural Tube Defects
| Allele Symbol | Sufutm1Aeb | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Allen E Bale | ||
| Allele Type | Targeted (knock-out) | ||
| Mutation Made By | Allen Bale, Yale University | ||
| Strain of Origin | 129S1/Sv-Oca2<+> Tyr<+> Kitl<+> | ||
| ES Cell Line Name | W9.5/W95 | ||
| ES Cell Line Strain | 129S1/Sv-Oca2<+> Tyr<+> Kitl<+> | ||
| Gene Symbol and Name | Sufu, suppressor of fused homolog (Drosophila) | ||
| Chromosome | 19 | ||
| Gene Common Name(s) | 2810026F04Rik; PRO1280; RIKEN cDNA 2810026F04 gene; SUFUH; SUFUXL; Su(Fu); | ||
| Molecular Note | Vector contains exon 4 through the 3' end of intron 6 then PGK-driven NEO in orientation reverse to the gene followed by the 3' end of exon 7 through the end of exon 8. Correct targeting replaces the intron 6/exon 7 splice site and a portion of exon 7 with the neo casette. Northern and Western blot analysis confirmed the absence of transcription and translation. [MGI Ref ID J:101731] | ||
Genotyping Protocols
Sufutm1Aeb, SEP PCR, vers. 1
Helpful Links
Optimizing PCR Protocols
Cooper AF; Yu KP; Brueckner M; Brailey LL; Johnson L; McGrath JM; Bale AE. 2005. Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused. Development 132(19):4407-17. [PubMed: 16155214] [MGI Ref ID J:101731]
Animal Health Reports
Room Number AX12
Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice are bred as heterozygotes. Homozygotes do not survive past embryonic day 10.5. Mating System +/+ sibling x Heterozygote (Female x Male) Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
|
Weeks of Age Price* Gender Genotypes Provided Individual Mouse Price $236.40 Female or Male Heterozygous for Sufutm1Aeb *Price(s) in US dollars ($)
Pairs /Price* Pair Genotype $288.65 Heterozygous for Sufutm1Aeb x Wild-type for Sufutm1Aeb $288.65 Wild-type for Sufutm1Aeb x Heterozygous for Sufutm1Aeb
| 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 $307.40 Female or Male Heterozygous for Sufutm1Aeb *Price(s) in US dollars ($)
Pairs /Price* Pair Genotype $375.30 Heterozygous for Sufutm1Aeb x Wild-type for Sufutm1Aeb $375.30 Wild-type for Sufutm1Aeb x Heterozygous for Sufutm1Aeb
| 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. |
|---|---|
| Supply Notes |
|
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 002448 129S1/SvImJ | (approximate) | |
| 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. | ||
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