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Type Mutant Strain; Spontaneous Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Description
The overall appearance of mice homozygous for either the Scd1ab-J allele or the Scd1ab-2J allele (Stock No. 002304 or 005956) includes slightly hunched posture, dry, scaly skin, thin fur sometimes detectable by 7 days of age, and small eyes with encrusted eyelids stuck shut. They have hypoplasia of the sebaceous glands and other hair follicle abnormalities that result in scarring alopecia. These mice have a paucity of adipose tissue, thin subcutis, and a distinctive odor. Hepatic cholesterol ester and triglyceride synthesis has been shown to be deficient in Scd1ab-J homozygotes and could not be restored through diet. Early studies of skin lipids in the original asebia mutant (Scd1ab) revealed a deficiency in wax esters, wax diesters, and sterols esterified with very long-chain fatty acids along with an increase in free sterols. (Wilkinson and Darasek, 1966; Sundberg et al., 1994; Zheng et al. 1999; Miyazaki et al., 2000; Sundberg et al., 2000)Mice homozygous for the Scd1ab-2J allele have greater dermal inflammatory infiltrate in the skin and thicker epidermis than do Scd1ab-J mice. Scd1ab-2J homozygotes show an increased transepidermal water loss and corresponding ad libitum intake of water that is not seen in Scd1ab-J homozygotes. For a thorough description see Sundberg et al., 2000 and Sundberg, 1994.
Development
The Scd1ab-2J allele arose in 1993 on the DBA/1LacJ background at The Jackson Laboratory. The mutation was maintained by sibling mating at each generation.
Strains carrying Scd1ab-2J allele
005956 B6;D1Lac-Scd1ab-2J/J View Strains carrying Scd1ab-2J (1 strain)
Strains carrying other alleles of Scd1
006201 B6.129-Scd1tm1Ntam/J View Strains carrying other alleles of Scd1 (1 strain)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Scd1ab-2J/Scd1ab-2J
DBA/1LacJ-Scd1ab-2J/J
- skin/coat/nails phenotype
- abnormal hair follicle morphology (MGI Ref ID J:62699)
- hair follicle bulbar histology is distorted compared to in wild-type mice
- hair shafts rupture through the base of the hair follicle and induce a foreign body granuloma in the dermal stroma resulting in dermal scarring and eventually scarring of the hair follicle
- while few follicles continue to cycle, with each cycle there is a progressive loss of individual follicles
- abnormal hair follicle development (MGI Ref ID J:62699)
- follicles stay in anagen longer than in wild-type mice
- abnormal hair follicle root sheath (MGI Ref ID J:62699)
- the inner root sheath is retained beyond the midfollicle into the outer piliary canal unlike in wild-type mice
- enlarged hair follicles (MGI Ref ID J:62699)
- during the first anagen stage the hair follicles are unusually long and extend at a sharp angle into the deep subcutis unlike in wild-type mice
- abnormal hair shaft morphology (MGI Ref ID J:62699)
- hair shafts rupture through the base of the hair follicle and induce a foreign body granuloma in the dermal stroma resulting in dermal scarring and eventually scarring of the hair follicle
- abnormal skin morphology (MGI Ref ID J:62699)
- mice exhibit thicker than normal epidermis, Malphigian layer and stratum corneum
- abnormal meibomian gland morphology (MGI Ref ID J:62699)
- small
- acanthosis (MGI Ref ID J:62699)
- hyperkeratosis (MGI Ref ID J:62699)
- mice exhibit varying degrees of orthokeratotic hyperkeratosis
- parakeratosis (MGI Ref ID J:62699)
- in focal areas
- sebaceous gland atrophy (MGI Ref ID J:62699)
- at day 6 mice have very small sebaceous glands compared to in wild-type mice
- mice have small meibomian, perianal and cerimous glands
- however, preputial, clitoral, lingual, Harderian and lacrimal glands are normal
- thick dermal layer (MGI Ref ID J:62699)
- dry skin (MGI Ref ID J:62699)
- flaky skin (MGI Ref ID J:62699)
- moderate white flaking is observed when hair is removed unlike in wild-type mice
- impaired skin barrier function (MGI Ref ID J:62699)
- transepidermal water loss is increased 4.5-fold compared to in wild-type mice
- matted coat (MGI Ref ID J:62699)
- scaly skin (MGI Ref ID J:62699)
- sparse hair (MGI Ref ID J:62699)
- behavior/neurological phenotype
- hunched posture (MGI Ref ID J:62699)
- increased drinking behavior (MGI Ref ID J:62699)
- homeostasis/metabolism phenotype
- abnormal lipid level (MGI Ref ID J:62699)
- mice exhibit a reduction in skin surface lipids such as sterol esters and cholesterol with a total loss of diol esters unlike in wild-type mice
- impaired skin barrier function (MGI Ref ID J:62699)
- transepidermal water loss is increased 4.5-fold compared to in wild-type mice
- immune system phenotype
- granulomatous inflammation (MGI Ref ID J:62699)
- hair shafts rupture through the base of the hair follicle and induce a foreign body granuloma in the dermal stroma resulting in dermal scarring and eventually scarring of the hair follicle
- renal/urinary system phenotype
- polyuria (MGI Ref ID J:62699)
- urine output is increased by 2% compared to in wild-type mice
- endocrine/exocrine gland phenotype
- abnormal meibomian gland morphology (MGI Ref ID J:62699)
- small
- sebaceous gland atrophy (MGI Ref ID J:62699)
- at day 6 mice have very small sebaceous glands compared to in wild-type mice
- mice have small meibomian, perianal and cerimous glands
- however, preputial, clitoral, lingual, Harderian and lacrimal glands are normal
- vision/eye phenotype
- abnormal meibomian gland morphology (MGI Ref ID J:62699)
- small
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Scd1ab-2J related
Cardiovascular Research
Hypotriglyceridemia
Dermatology Research
Skin and Hair Texture Defects
Internal/Organ Research
Adipose Defects
Metabolism Research
Lipid Metabolism
| Allele Symbol | Scd1ab-2J | ||
|---|---|---|---|
| Allele Name | asebia 2 Jackson | ||
| Allele Type | Spontaneous | ||
| Strain of Origin | DBA/1LacJ | ||
| Gene Symbol and Name | Scd1, stearoyl-Coenzyme A desaturase 1 | ||
| Chromosome | 19 | ||
| Gene Common Name(s) | AA589638; AI265570; SCD; Scd-1; ab; asebia; expressed sequence AA589638; expressed sequence AI265570; stearoyl-CoA desaturase; | ||
| Molecular Note | An 18 bp deletion in the exon 2/intron 2 boundary. [MGI Ref ID J:58283] | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Ntambi JM; Buhrow SA; Kaestner KH; Christy RJ; Sibley E; Kelly TJ Jr; Lane MD. 1988. Differentiation-induced gene expression in 3T3-L1 preadipocytes. Characterization of a differentially expressed gene encoding stearoyl-CoA desaturase. J Biol Chem 263(33):17291-300. [PubMed: 2903162] [MGI Ref ID J:9448]
Sundberg JP; Boggess D; Sundberg BA; Eilertsen K; Parimoo S; Filippi M; Stenn K. 2000. Asebia-2J (Scd1(ab2J)): a new allele and a model for scarring alopecia. Am J Pathol 156(6):2067-75. [PubMed: 10854228] [MGI Ref ID J:62699]
Wilkinson DI; Karasek MA. 1966. Skin lipids of a normal and mutant (asebic) mouse strain. J Invest Dermatol 47(5):449-55. [PubMed: 5924301] [MGI Ref ID J:5013]
Zheng Y; Eilertsen KJ; Ge L; Zhang L; Sundberg JP; Prouty SM; Stenn KS; Parimoo S. 1999. Scd1 is expressed in sebaceous glands and is disrupted in the asebia mouse [letter] Nat Genet 23(3):268-70. [PubMed: 10545940] [MGI Ref ID J:58283]
Scd1ab-2J relatedMacDonald ML; Singaraja RR; Bissada N; Ruddle P; Watts R; Karasinska JM; Gibson WT; Fievet C; Vance JE; Staels B; Hayden MR. 2008. Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice. J Lipid Res 49(1):217-29. [PubMed: 17960025] [MGI Ref ID J:130278]
Sundberg JP; Boggess D; Sundberg BA; Eilertsen K; Parimoo S; Filippi M; Stenn K. 2000. Asebia-2J (Scd1(ab2J)): a new allele and a model for scarring alopecia. Am J Pathol 156(6):2067-75. [PubMed: 10854228] [MGI Ref ID J:62699]
Zheng Y; Eilertsen KJ; Ge L; Zhang L; Sundberg JP; Prouty SM; Stenn KS; Parimoo S. 1999. Scd1 is expressed in sebaceous glands and is disrupted in the asebia mouse [letter] Nat Genet 23(3):268-70. [PubMed: 10545940] [MGI Ref ID J:58283]
Colony Maintenance
Breeding & Husbandry The homozygotes are very poor breeders and the mutation was best maintained using heterozygous females bred to homozygous males. It was also frozen using this breeding scheme.
| Pricing for USA, Canada and Mexico shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 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.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 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 for further information. |
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| Supply Notes |
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Purchasing Information
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Contact Information
Orders & Technical Support
Tel: 800.422.6423 or 207.288.5845
Fax: 207.288.6150
Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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