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Last modified on June 1, 2010 The Mouse Strain Difference Page
Click here to see common conditions with lists of affected strains.
129 strainsIn October 1998, the International Committee on Genetic Nomenclature for Mice approved a new nomenclature for 129 strains, because there are differences between the sublines. These changes affect strain designations for inbred 129 mice and all transgenics and mutants derived from them. Detailed information is available at http://jaxmice.jax.org/html/nomenclature/nomen_129.shtml {4181} All 129 substrains are homozygous for white-bellied agouti allele of the agouti (Aw) gene. Some substrains are not typical agouti color because of various epistatic genes, such as albino (Tyrc), pink-eyed dilution (p) or steel (Mgfsl). The ES cells of 129 mice are frequently used in the generation of targeted mutations. ES cells are introduced into C57BL/6 blastocysts, which are chosen because they have the black allele (a/a) at the agouti gene. The degree of contribution by the ES cell can be estimated by visual examination of the chimeric progeny for agouti color. Aw is dominant over a. In the first backcross with C57BL/6, some mice will be Aw/a if the ES cell contributed to the germline and will therefore be agouti. However, only half of these agouti offspring will carry the targeted allele, since the original ES cells were heterozygous. Other offspring in the first backcross will be black (a/a), since some of the gametes from the chimera will have been derived from the parent C57BL/6 mouse.{3740}
AVery susceptible to mousepox, dying acutely{3763}; Ectromelia is worse in A, CBA, DBA, C3H, BALB/c mice{3577} Common tumors are mammary and pulmonary (CL Davis 2001)
AKRResistant to mousepox{3763} Lactate dehydrogenase virus: AKR, C58 mice are paralyzed{3577}, but this turned out to be demyelination in previously retrovirus-infected animals{3763}{3551}. Common tumor: leukemia (CL Davis 2001)
AXB recombinant inbredProgenitors were A/J and C57BL/6J; used for genetics research (gene mapping), inflammation (genes regulating infectious disease and endotoxin susceptibility) and neurobiology (genes regulating preference to alcohol and stress); many strains in albino, black or brown{4181} Helicobacter hepaticus: These mice (derived from A/JCr x C57Bl/6J) are used for studying the host response to infectious agents, according to Fox{4047}. They found that 9 strains tested by gavaging with Helicobacter hepaticus differed in their susceptibility and response to the disease, and that hepatic neoplasia incidence was higher than in A/JCr historical controls. BALB/cAlbino mice of several substrains (including cByJ and cJ at Jax); increased incidence of late-onset mammary gland tumors; neurodevelopmental defects (callosal agenesis); used to produce monoclonal antibodies, myeloma and hybridoma, and is the background strain for histocompatibility genetics studies. The BALB/cWtEi substrain has early Y-chromosome nondisjunction resulting in hermaphroditism and sex chromosome chimerism.{4181} Also has age-related hearing loss and dystrophic cardiac calcification{4182}. Letters stand for "Bagg albino". BALB/cJ are extremely aggressive, while BALB/cByJ are much less so. although the strains differ at only 3 genetic loci{4184}. Helicobacter felis: develop minimal inflammation{3845} Borrelia burgdorferi: intermediate susceptibility; C3H/He are most affected, C57BL/6 mildly{4015} Salmonella is worse in BALB/C, C57BL mice{3577} Ectromelia is worse in A, CBA, DBA, C3H, BALB/c mice{3577} MHV is worse in BALB/c, C57BL mice{3577}; BALB/c are better sentinels Carry genes conferring resistance to encephalomyocarditis virus by influencing interferon{4162}. Dermatitis due to Myocoptes musculinis occurs in BALB/c, but no dermatitis occurs in response to Myobia musculi{4096} Mouse parvovirus (MPV): High doses are needed to get a measurable humoral response. C3H/HeN mice are good responders; ICN, BALB/c and DBA/2 mice are pretty good; and C57BL/6 require high doses and still they don't all seroconvert {4103}. CBA and C57BL mice have been reported to be less sensitive to morphine than DBA and BALB{4138}. Very sensitive to ether, along with DBA/2 and C3H/He{4154} C3HNote that the entire strain designation is important as there are significant differences. C3HeB/FeJ does not carry MMTV{4184}. They are agouti and have retinal degeneration (they are models for human retinitis pigmentosa) due to homozygosity for the rd1 mutation of the gene Pdeb{4182}. They have increased tumors (hepatomas, late-onset mammary gland). They are listed as "general purpose" research tools.{4181} Their bone mass is relatively high (c.f. C57BL/6). The strain was derived from Bagg albino x DBA, and has the same predilection for dystrophic cardiac calcification{4182}. Ectromelia is worse in A, CBA, DBA, C3H, BALB/c mice{3577};very susceptible to mousepox, dying acutely{3763}
C57BL/6Black mice with high susceptibility to diet-induced atherosclerosis (the most susceptible of all strains{4184}), obesity and diabetes. Have old-age-related hearing loss ~12-18 months. Are a background strain for histocompatibility congenics. C57BL/6J are also used for developmental biology research (eye and skeletal defects), type II diabetes (NIDDM, diet-induced), mutagenesis and transgenesis, behavioral and learning defects.{4181} They have low bone mass (c.f. C3H which have high bone mass), ulcerative dermatitis, pigmentation of the spleen, meninges, dura, and heart valves, microphthalmia (up to 12% incidence, mostly in females), cataracts and other ocular abnormalities, and hydrocephalus(1%){4182}. They have a high preference for alcohol, morphine and other opioids. They are good breeders but the females may die with their first litter; hydrocephalus at 4 weeks of age is common{4184}. Lethal effects of ether: C57BL/6 most resistant, followed by ICR. Sleep a long time under pentobarbital, second to DBA.{4154} Helicobacter felis: develop severe inflammation{3845} C57BL/6J mice are resistant to H. hepaticus-induced disease{4047} Resistant to mousepox{3763}; in fact, this strain is the most resistant. H-2 and non-H-2 genes are responsible; C57BL mice have a shorter period of virus transmission to the lymphoreticular system, and females are more resistant than males to some strains of virus{4162}. Borrelia burgdorferi: least affected; C3H/He are most susceptible, BALB/c intermediate{4015} Sendai virus: Mice strains vary in susceptibility to Sendai virus because of mucociliary clearance; resistant strains include AKR/J, Swiss, C57BL/6J, RF/J, and SJL/J{3551}. In C57BL/6J mice, resistance is conferred by an autosomal dominant trait on chromosome 1{4162}. Salmonella is worse in BALB/C, C57BL mice{3577} MHV is worse in BALB/C, C57BL mice{3577} Dermatitis is worse in C57BL/6 mice due to Myobia musculi{4096} Mouse parvovirus (MPV): High doses are needed to get a measurable humoral response. C3H/HeN mice are good responders; ICN, BALB/c and DBA/2 mice are pretty good; and C57BL/6 require high doses and still they don't all seroconvert {4103}. CBA and C57BL mice have been reported to be less sensitive to morphine than DBA and BALB{4138}. C57BL/6 mice breathe more shallowly, less deeply, and more regularly than A/J mice, both awake and under urethane anesthesia.{4733} C57BL/6JThese mice, when carrying the db or ob mutations, have high plasma insulin and hypertrophied islets of Langerhans{4162} C57BL/Ks (C57BLKS {4181})A black mouse with NIDDM and age-related hearing loss <3 months. Used for "general purposes", diabetes research, vestibular and hearing defects.{4181} They have a high frequency of malformed toes, polycystic kidneys and microphthalmia{4184}. Mice carrying the db or ob mutations on this background have decreased plasma insulin and degenerated islets of Langerhans{4162} C58Black mice with occasional white spots on belly{4184}. Increased incidence of leukemia{4181}, used in genetics, immunology, molecular biology, oncology and virology.{4184} Lactate dehydrogenase virus: AKR, C58 mice are paralyzed{3577}, but this turned out to be demyelination in previously retrovirus-infected animals{3763}{3551}. CBAAgouti mice with increased incidence of hepatomas, lymphomas and late-onset mammary gland tumors. The CBA/J substrain also has retinal degeneration and is used for research in retinitis pigmentosa. Another strain (CBA/CaHN-Btkxid/J) is used to study Bruton agammaglobulinemia tyrosine kinase{4181} because of sex-linked immunodeficiency{4184}. Obtained from a cross of Bagg albino x DBA in 1920. CBA/J is the only CBA substrain carrying the Pdebrd1 allele for retinal degeneration.{4184} Ectromelia is worse in A, CBA, DBA, C3H, BALB/c mice{3577} CBA and C57BL mice have been reported to be less sensitive to morphine than DBA and BALB{4138}. CBA mice sleep a long time under pentobarbital, second to DBA and C57Bl/6.{4154} DBADilute brown non-agouti mice used for general purposes. See specifics for substrains.{4181} Gets dystrophic calcification of the heart, kidneys, tongue, and other soft tissues which maps to chromosome 7{4182}. The dilute coat color is due to mutation caused by integration of a retrovirus at the d locus.{4749} Ectromelia is worse in A, CBA, DBA, C3H, BALB/c mice{3577} CBA and C57BL mice have been reported to be less sensitive to morphine than DBA and BALB{4138}. DBAs are more sensitive to pentobarbital than other strains.{4154}
ddYMycoplasma pulmonis is worse in ddY mice; LEW rats{3577} FVBFVB/NJ
NC/Jic and NC/NgaVery susceptible to dermatitis caused by Myobia musculi{4096} Nude
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©1999, Janet Becker Rodgers, DVM, MS, DipACLAM, MRCVS All rights reserved. Comments? Send an email to janet.rodgers@vet.ox.ac.uk |