Strain Name:

B6.129-Indotm1Alm/J

Stock Number:

005867

Availability:

Repository- Live

Use Restrictions Apply, see Terms of Use

Description

Strain Information

Type Congenic; Mutant Strain; Targeted Mutation;
Additional information on Genetically Engineered Mutant Mice.
Mating SystemHomozygote x Homozygote         (Female x Male)
Specieslaboratory mouse
Generation?+N1F6 (05-AUG-08)
 
Donating Investigator Andrew Mellor,   Medical College of Georgia

Description
Homozygous mice are viable and fertile with normal immune system development and function. They exhibit no spontaneous autoimmune disorders. No gene product (mRNA or protein) from the targeted gene is detected in the epididymis. At embryonic day 10.5, endogenous protein is absent from all cells at the maternal-fetal interface when both parents are homozygous for the targeted gene. Allogeneic and syngeneic pregnancy outcomes are unaffected by this mutation. In contrast to wildtype, anti-proliferative treatments (CTLA4-Ig, IFNalpha, or CpG-ODN) do not suppress T cell expansion both in vivo and in vitro. In addition, homozygous dendritic cells isolated from lymph nodes draining (induced) tumor sites have no suppressor activity. These mice may be useful in studies of pregnancy and reproductive immunology (tryptophan degradation, T cell activation, clonal expansion) as well as autoimmune disease, tissue transplantation, fostering, acquired tolerance/T cell anergy, and immunosuppressive pathways.

Development
A targeting vector was designed to replace exons 3-5 (encode critical portions of the enzyme catalytic site) with the beta-galactosidase and neomycin resistance genes. Additionally, a translational "stop" codon (TAG) was introduced into exon 2. The construct was electroporated into 129/SvJ-derived embryonic stem (ES) cells and correctly targeted clones were injected into blastocysts. Male chimeric mice were mated with C57BL/6 females to produce heterozygotes. Mutant mice were backcrossed more than 10 generations to C57BL/6 before arriving at The Jackson Laboratory.

Control Information

  Control
   000664 C57BL/6J
 
  Considerations for Choosing Controls

Additional Web Information

Congenic Nomenclature

Phenotype

Phenotype Information

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.

Indotm1Alm/Indotm1Alm

        either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * CBA)
  • reproductive system phenotype
  • *normal* reproductive system phenotype (MGI Ref ID J:93797)
    • no effect on reproductive success
View Research Applications

Research Applications
This mouse can be used to support research in many areas including:

Immunology and Inflammation Research
Autoimmunity
Immunodeficiency (T cell deficiency)

Research Tools
Cancer Research (B and T cell deficiency) (xenograft/transplant host)
Immunology and Inflammation Research (T cell deficiency) (xenograft/transplant host)
Reproductive Biology Research

Genes & Alleles

Gene & Allele Information

Allele Symbol Indotm1Alm
Allele Name targeted mutation 1, Andrew L Mellor
Allele Type Targeted (knock-out)
Common Name(s) IDO-;
Mutation Made By Brendan Marshall,   Medical College of Georgia
Strain of Origin129X1/SvJ
ES Cell Line Strain129
Gene Symbol and Name Indo, indoleamine-pyrrole 2,3 dioxygenase
Chromosome 8
Gene Common Name(s) CD107B; IDO; IDO1; Ido; indole 2,3-dioxygenase; indole 2,4-dioxygenase;
Molecular Note A Betagal and neomycin cassette replaced exons 3-5, which encode critical portions of the enzyme catalytic site. Also, a translation stop codon was introduced into exon 2. RT-PCR of total epididymis RNA from mutants showed no transcript was present. Western blot of mutant epididymis confirmed a lack of protein. [MGI Ref ID J:93797]

Genotyping

Genotyping Information

Genotyping Protocols

Indotm1Alm, STD PCR, vers. 1

Helpful Links

Optimizing PCR Protocols

References

References

Selected Reference(s)

Baban B; Chandler P; McCool D; Marshall B; Munn DH; Mellor AL. 2004. Indoleamine 2,3-dioxygenase expression is restricted to fetal trophoblast giant cells during murine gestation and is maternal genome specific. J Reprod Immunol 61(2):67-77. [PubMed: 15063630]  [MGI Ref ID J:93797]

Additional References

Indotm1Alm related

Baban B; Hansen AM; Chandler PR; Manlapat A; Bingaman A; Kahler DJ; Munn DH; Mellor AL. 2005. A minor population of splenic dendritic cells expressing CD19 mediates IDO-dependent T cell suppression via type I IFN signaling following B7 ligation. Int Immunol 17(7):909-19. [PubMed: 15967784]  [MGI Ref ID J:99971]

Harrington L; Srikanth CV; Antony R; Rhee SJ; Mellor AL; Shi HN; Cherayil BJ. 2008. Deficiency of indoleamine 2,3-dioxygenase enhances commensal-induced antibody responses and protects against Citrobacter rodentium-induced colitis. Infect Immun 76(7):3045-53. [PubMed: 18426872]  [MGI Ref ID J:137302]

Jasperson LK; Bucher C; Panoskaltsis-Mortari A; Taylor PA; Mellor AL; Munn DH; Blazar BR. 2008. Indoleamine 2,3-dioxygenase is a critical regulator of acute graft-versus-host disease lethality. Blood 111(6):3257-65. [PubMed: 18077788]  [MGI Ref ID J:132719]

Manlapat AK; Kahler DJ; Chandler PR; Munn DH; Mellor AL. 2007. Cell-autonomous control of interferon type I expression by indoleamine 2,3-dioxygenase in regulatory CD19+ dendritic cells. Eur J Immunol 37(4):1064-71. [PubMed: 17343295]  [MGI Ref ID J:120813]

Mellor AL; Baban B; Chandler P; Marshall B; Jhaver K; Hansen A; Koni PA; Iwashima M; Munn DH. 2003. Cutting edge: induced indoleamine 2,3 dioxygenase expression in dendritic cell subsets suppresses T cell clonal expansion. J Immunol 171(4):1652-5. [PubMed: 12902462]  [MGI Ref ID J:93796]

Mellor AL; Baban B; Chandler PR; Manlapat A; Kahler DJ; Munn DH. 2005. Cutting edge: CpG oligonucleotides induce splenic CD19+ dendritic cells to acquire potent indoleamine 2,3-dioxygenase-dependent T cell regulatory functions via IFN Type 1 signaling. J Immunol 175(9):5601-5. [PubMed: 16237046]  [MGI Ref ID J:119367]

Mellor AL; Chandler P; Baban B; Hansen AM; Marshall B; Pihkala J; Waldmann H; Cobbold S; Adams E; Munn DH. 2004. Specific subsets of murine dendritic cells acquire potent T cell regulatory functions following CTLA4-mediated induction of indoleamine 2,3 dioxygenase. Int Immunol 16(10):1391-401. [PubMed: 15351783]  [MGI Ref ID J:93639]

Xu H; Oriss TB; Fei M; Henry AC; Melgert BN; Chen L; Mellor AL; Munn DH; Irvin CG; Ray P; Ray A. 2008. Indoleamine 2,3-dioxygenase in lung dendritic cells promotes Th2 responses and allergic inflammation. Proc Natl Acad Sci U S A 105(18):6690-5. [PubMed: 18436652]  [MGI Ref ID J:134645]

Health & husbandry

Health & Colony Maintenance Information

Animal Health Reports

Room Number           AX11

Colony Maintenance

Breeding & HusbandryWhen maintaining a live colony, these mice are bred as heterozygotes or homozygotes.
Mating SystemHomozygote x Homozygote         (Female x Male)
Diet Information LabDiet® 5K52/5K67

Purchasing information

Pricing, Supply Level & Notes, Controls, General Terms & Conditions

Pricing

Pricing for USA, Canada and Mexico shipping destinations View International pricing
Weeks of AgePrice*GenderGenotypes Provided
Individual Mouse Price $155.60Female or MaleHomozygous for Indotm1Alm
Pairs /Price*Pair Genotype
$311.20Homozygous for Indotm1Alm x Homozygous for Indotm1Alm
*Price(s) in US dollars ($)

Additional Supply Details

Supply Notes

Pricing for International shipping destinations View USA Canada and Mexico pricing
Weeks of AgePrice*GenderGenotypes Provided
Individual Mouse Price $202.30Female or MaleHomozygous for Indotm1Alm
Pairs /Price*Pair Genotype
$404.60Homozygous for Indotm1Alm x Homozygous for Indotm1Alm
*Price(s) in US dollars ($)

Additional Supply Details

Supply Notes

Supply Details

Standard SupplyRepository-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 Information

  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.

General Terms and Conditions


See Terms of Use


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The Jackson Laboratory has rigorous genetic quality control and mutant gene genotyping programs to ensure the genetic background of JAX® Mice strains as well as the genotypes of strains with identified molecular mutations. JAX® Mice strains are only made available to researchers after meeting our standards. However, the phenotype of each strain may not be fully characterized and/or captured in the strain data sheets. Therefore, we cannot guarantee a strain's phenotype will meet all expectations. To ensure that JAX® Mice will meet the needs of individual research projects or when requesting a strain that is new to your research, we suggest ordering and performing tests on a small number of mice to determine suitability for your particular project.
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Terms of Use

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General Terms and Conditions


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phone:207-288-6470
fax:207-288-6655

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