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Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered Mutant Mice. Generation N12p+F1pN1 Donating Investigator Stanley Korsmeyer, Dana-Farber Cancer Institute 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 mice are embryonic lethal. These mutant mice may be useful in studies of immune function, including apoptosis, B and T cell development, and bone marrow cell differentiation.When bred to a strain with loxP sites inserted into the same targeted allele (Stock No. 006088) and a strain with a Cd19 null allele and expressing Cre recombinase during the B lymphocyte development (Stock No. 004126), this mutant mouse strain may be useful in studies of lymphocyte development.
When bred to a strain with loxP sites inserted into the same targeted allele (Stock No. 006088) and a strain expressing interferon inducible Cre recombinase in the lymphocytes (Stock No. 003556), this mutant mouse strain may be useful in studies of lymphocyte development.
Development
A targeting vector containing an internal ribosomal entry site (IRES) fused to a neomycin-beta-galactosidase fusion protein (beta-geo) was used to replace a portion from within exon 1 to within exon 2 of the endogenous gene. This construct was electroporated into 129X1/SvJ-derived RW4 embryonic stem (ES) cells. Correctly targeted ES cells were injected in C57BL/6 balstocysts and the resulting chimeric mice were crossed to C57BL/6J. Heterozygotes were backcrossed to C57BL/6J mice for more than 10 generations prior to arrival at The Jackson Laboratory.
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
Strains carrying other alleles of Mcl1
006088 B6;129-Mcl1tm3Sjk/J View Strains carrying other alleles of Mcl1 (1 strain)
Congenic Nomenclature
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
The following phenotype relates to a compound genotype created using this strain.
Contact JAX® Services jaxservices@jax.org for customized breeding options.Cd19tm1(cre)Cgn/Cd19+ Mcl1tm2Sjk/Mcl1tm3Sjk
involves: 129X1/SvJ (conditional)
- hematopoietic system phenotype
- abnormal B cell differentiation (MGI Ref ID J:86906)
- absent early pro-B cells (MGI Ref ID J:86906)
- absent late pro-B cells (MGI Ref ID J:86906)
- absent pre-B cells (MGI Ref ID J:86906)
- arrested B cell differentiation (MGI Ref ID J:86906)
- arrested at pro-B cell stage
- decreased B cell number (MGI Ref ID J:86906)
- decrease in peripheral B cells
- 88% reduction of splenic B cells relative to controls
- near absence of lymph node B cells
- detected peripheral B cells did not undergo cre-mediated recombination
- absent pre-B cells (MGI Ref ID J:86906)
- increased B cell apoptosis (MGI Ref ID J:86906)
- increased apoptosis at pro-B cell stage
- immune system phenotype
- abnormal B cell differentiation (MGI Ref ID J:86906)
- absent early pro-B cells (MGI Ref ID J:86906)
- absent late pro-B cells (MGI Ref ID J:86906)
- absent pre-B cells (MGI Ref ID J:86906)
- arrested B cell differentiation (MGI Ref ID J:86906)
- arrested at pro-B cell stage
- decreased B cell number (MGI Ref ID J:86906)
- decrease in peripheral B cells
- 88% reduction of splenic B cells relative to controls
- near absence of lymph node B cells
- detected peripheral B cells did not undergo cre-mediated recombination
- absent pre-B cells (MGI Ref ID J:86906)
- increased B cell apoptosis (MGI Ref ID J:86906)
- increased apoptosis at pro-B cell stage
Mcl1tm2Sjk/Mcl1tm3Sjk Tg(Mx1-cre)1Cgn/0
involves: 129X1/SvJ (conditional)
- hematopoietic system phenotype
- decreased B cell number (MGI Ref ID J:86906)
- peripheral B cells are not maintained
- decreased T cell number (MGI Ref ID J:86906)
- peripheral T cells are not maintained
- immune system phenotype
- decreased B cell number (MGI Ref ID J:86906)
- peripheral B cells are not maintained
- decreased T cell number (MGI Ref ID J:86906)
- peripheral T cells are not maintained
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Apoptosis Research
Endogenous Regulators
Developmental Biology Research
Embryonic Lethality (Homozygous)
Immunology and Inflammation Research
Autoimmunity (B and T cell deficiency)
Immunodeficiency (B and T cell deficiency)
Inflammation (B and T cell deficiency)
Lymphoid Tissue Defects (B and T cell deficiency)
Lymphoid Tissue Defects (hematopoietic development)
Research Tools
Apoptosis Research
Developmental Biology Research
Immunology and Inflammation Research (B and T cell deficiency)
| Allele Symbol | Mcl1tm2Sjk | ||
|---|---|---|---|
| Allele Name | targeted mutation 2, Stanley J Korsmeyer | ||
| Allele Type | Targeted (Reporter) | ||
| Common Name(s) | Mcl-1null; Mcl1-bGeo; | ||
| Mutation Made By | Stanley Korsmeyer, Dana-Farber Cancer Institute | ||
| Gene Symbol and Name | Mcl1, myeloid cell leukemia sequence 1 | ||
| Chromosome | 3 | ||
| Gene Common Name(s) | AW556805; BCL2L3; EAT; MCL1L; MCL1S; MGC104264; MGC1839; Mcl-1; TM; expressed sequence AW556805; | ||
| Molecular Note | A sequence fragment extending from within exon 1 through a 5' portion of exon 2 was replaced with an IRES-betageo cassette. Western blot analysis of mutant murine embryonic fibroblasts indicated that no normal protein is produced from this allele. [MGI Ref ID J:86906] | ||
Genotyping Protocols
Mcl1tm2Sjk, STD PCR, vers. 1
Helpful Links
Optimizing PCR Protocols
Opferman JT; Letai A; Beard C; Sorcinelli MD; Ong CC; Korsmeyer SJ. 2003. Development and maintenance of B and T lymphocytes requires antiapoptotic MCL-1. Nature 426(6967):671-6. [PubMed: 14668867] [MGI Ref ID J:86906]
Mcl1tm2Sjk relatedOpferman JT; Iwasaki H; Ong CC; Suh H; Mizuno S; Akashi K; Korsmeyer SJ. 2005. Obligate role of anti-apoptotic MCL-1 in the survival of hematopoietic stem cells. Science 307(5712):1101-4. [PubMed: 15718471] [MGI Ref ID J:96127]
Woodland RT; Fox CJ; Schmidt MR; Hammerman PS; Opferman JT; Korsmeyer SJ; Hilbert DM; Thompson CB. 2008. Multiple signaling pathways promote B lymphocyte stimulator dependent B-cell growth and survival. Blood 111(2):750-60. [PubMed: 17942753] [MGI Ref ID J:130058]
Colony Maintenance
Breeding & Husbandry When maintaining a live colony, these mice are bred as heterozygotes. Homozygous mice die in utero.
| Pricing for USA, Canada and Mexico shipping destinations |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $1900.00
| Pricing for International shipping destinations |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $2470.00
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information. |
|---|---|
| Supply Notes |
|
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 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. | ||
Purchasing Information
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