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| Mice that are homozygous for this targeted mutation on the 129S genetic background exhibit diminished social interaction behavior, do not barber or trim whiskers of cagemates, show subordinance in social dominance tests, do not sleep huddled together and do not build nests. This mutant mouse strain may be useful in studies of social behavior, sensorimotor gating, and possibly psychiatric disorders. | |||||||
Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered Mutant Mice. Mating System Homozygote x Homozygote (Female x Male) Species laboratory mouse Generation N15+F1 (29-APR-08) Donating Investigator Anthony Wynshaw-Boris, UCSD Description
Mice that are homozygous for the targeted mutation are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities. No gene product (protein) is detected by Western blot analysis of MEF (mouse embryonic fibroblasts) derived from homozygotes. Homozygotes exhibit diminished social interaction behavior, do not barber or trim whiskers of cagemates, show subordinance in social dominance tests, do not sleep huddled together and do not build nests. Although mutants have an attenuated prepulse inhibition of acoustic and tactile startle (sensorimotor gating of the startle reflex), they do not exhibit any deficits in locomotor or cognitive function. This mutant mouse strain may be useful in studies of social behavior, sensorimotor gating, and possibly psychiatric disorders.In an attempt to offer alleles on well-characterized or multiple genetic backgrounds, alleles are frequently moved to a genetic background different from that on which an allele was first characterized. This is the case for the strain above. It should be noted that the phenotype could vary from that originally described. We will modify the strain description if necessary as published results become available.
Development
A targeting vector containing neomycin resistance and herpes simplex virus thymidine kinase genes was used to disrupt part of exon 2 and exons 3 and 4, encoding amino acids 131-225. The construct was electroporated into 129S6/SvEvTac derived TC-1 embryonic stem (ES) cells. Correctly targeted ES cells were injected into recipient blastocysts. The resulting chimeric animals were crossed to mice, and then backcrossed to C57BL/6J for 15 generations.
| Control | ||
|---|---|---|
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
Strains carrying Dvl1tm1Awb allele
007965 129S-Dvl1tm1Awb/J View Strains carrying Dvl1tm1Awb (1 strain)
Congenic Nomenclature
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.
Dvl1tm1Awb/Dvl1tm1Awb
129S/SvEv
- behavior/neurological phenotype
- abnormal huddling behavior (MGI Ref ID J:42758)
- mice slept in scattered random patterns
- over a period of time, mutant mice tended to loosely huddle in various quandrants of the cage, whereas wild-type littermates were more often observed huddled in the same quadrant
- abnormal nest building behavior (MGI Ref ID J:42758)
- mice built smaller nests than wild-type littermates
- mutant mice were also observed spleeping on top of intact nestlet material
- whisker trimming (MGI Ref ID J:42758)
- mutant mice did not trim/barber their cagemates' whiskers or facial hair, whereas the majority of separately housed wild-type littermates displayed whisker trimming behavior
- nervous system phenotype
- reduced sensorimotor gating (MGI Ref ID J:42758)
- attenuation of acoustic pre-pulse inhibition was exhibited with both acoustic and tactile startle
- hearing/vestibular/ear phenotype
- *normal* hearing/vestibular/ear phenotype (MGI Ref ID J:100861)
- normal stereocilia orientation at E18.5
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Neurobiology Research
Behavioral and Learning Defects
Sensorineural Research
| Allele Symbol | Dvl1tm1Awb | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Anthony Wynshaw-Boris | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | Dvl1-; Dvl1del131-225; | ||
| Mutation Made By | Anthony Wynshaw-Boris, UCSD | ||
| Strain of Origin | 129S6/SvEvTac | ||
| ES Cell Line Name | TC-1 | ||
| ES Cell Line Strain | 129S6/SvEvTac | ||
| Gene Symbol and Name | Dvl1, dishevelled, dsh homolog 1 (Drosophila) | ||
| Chromosome | 4 | ||
| Gene Common Name(s) | DVL; MGC54245; dvl-1; | ||
| Molecular Note | A neomycin selection cassette replaced a genomic fragment containing part of exon 2 and exons 3 and 4, which encode amino acids 131-225. Western blot analysis on embryonic fibroblasts derived from homozygous mice confirmed that no detectable protein wasproduced from this allele. [MGI Ref ID J:42758] | ||
Genotyping Protocols
Dvl1tm1Awb, STD PCR, vers. 1
Helpful Links
Optimizing PCR Protocols
Lijam N; Paylor R; McDonald MP; Crawley JN; Deng CX; Herrup K ; Stevens KE ; Maccaferri G ; McBain CJ ; Sussman DJ ; Wynshaw-Boris A. 1997. Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1. Cell 90(5):895-905. [PubMed: 9298901] [MGI Ref ID J:42758]
Dvl1tm1Awb relatedAhmad-Annuar A; Ciani L; Simeonidis I; Herreros J; Fredj NB; Rosso SB; Hall A; Brickley S; Salinas PC. 2006. Signaling across the synapse: a role for Wnt and Dishevelled in presynaptic assembly and neurotransmitter release. J Cell Biol 174(1):127-39. [PubMed: 16818724] [MGI Ref ID J:111190]
Hamblet NS; Lijam N; Ruiz-Lozano P; Wang J; Yang Y; Luo Z; Mei L; Chien KR; Sussman DJ; Wynshaw-Boris A. 2002. Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure. Development 129(24):5827-38. [PubMed: 12421720] [MGI Ref ID J:79834]
Long JM; LaPorte P; Paylor R; Wynshaw-Boris A. 2004. Expanded characterization of the social interaction abnormalities in mice lacking Dvl1. Genes Brain Behav 3(1):51-62. [PubMed: 14960015] [MGI Ref ID J:101889]
Purro SA; Ciani L; Hoyos-Flight M; Stamatakou E; Siomou E; Salinas PC. 2008. Wnt regulates axon behavior through changes in microtubule growth directionality: a new role for adenomatous polyposis coli. J Neurosci 28(34):8644-54. [PubMed: 18716223] [MGI Ref ID J:138829]
Rosso SB; Sussman D; Wynshaw-Boris A; Salinas PC. 2005. Wnt signaling through Dishevelled, Rac and JNK regulates dendritic development. Nat Neurosci 8(1):34-42. [PubMed: 15608632] [MGI Ref ID J:95820]
Wang J; Hamblet NS; Mark S; Dickinson ME; Brinkman BC; Segil N; Fraser SE; Chen P; Wallingford JB; Wynshaw-Boris A. 2006. Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation. Development 133(9):1767-78. [PubMed: 16571627] [MGI Ref ID J:108512]
Wang J; Mark S; Zhang X; Qian D; Yoo SJ; Radde-Gallwitz K; Zhang Y; Lin X; Collazo A; Wynshaw-Boris A; Chen P. 2005. Regulation of polarized extension and planar cell polarity in the cochlea by the vertebrate PCP pathway. Nat Genet 37(9):980-5. [PubMed: 16116426] [MGI Ref ID J:100861]
Animal Health Reports
Room Number AX11
Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice can be bred as homozygotes. Mating System Homozygote x Homozygote (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 $155.70 Female or Male Homozygous for Dvl1tm1Awb *Price(s) in US dollars ($)
Pairs /Price* Pair Genotype $311.40 Homozygous for Dvl1tm1Awb x Homozygous for Dvl1tm1Awb
| 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 $202.50 Female or Male Homozygous for Dvl1tm1Awb *Price(s) in US dollars ($)
Pairs /Price* Pair Genotype $404.90 Homozygous for Dvl1tm1Awb x Homozygous for Dvl1tm1Awb
| 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 | ||
|---|---|---|
| 000664 C57BL/6J | ||
| 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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| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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