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Available Mouse Lines

The Mutant Mouse Regional Resource Center (MMRRC) exists to serve the research community by preserving biomedically valuable mouse strains and distributing these strains to the research community for internal, non-commercial research purposes.

 

Pkrkr Overexpression Model  
MMRRC Strain ID: 0132-H/M
This is a biochemical model for looking at translational events in protein synthesis, including the following mechanistic processes: muscle development and function, biology of aging, heat shock, viral infection, stress-induced apoptosis, and cancer in relation to selective inhibition of protein synthesis and translation.
Genotype:

Random integration of human PKR cDNA under control of the CMV promoter.

Phenotype: Spleen cells are resistant to apoptosis when treated with Actinomycin D and show a decrease in proliferation in response to Concanavalin A.
Primary Citation: Ladiges W, Morton J, Hopkins H, Wilson R, Filley G, Ware C, Gale M.  Expression of Human PKR Protein Kinase in Transgenic Mice.  Journal of Interferon and Cytokine Research (2002) 22: 329 – 334

Medline Accession:

 

# 12034040

 

WRN Overexpression Model 
MMRRC Strain ID: 0130-H/M
This is a novel mouse model for studying Werner Syndrome and other age-related disorders.
Genotype:

Random integration of human cDNA containing a single amino acid substitution at position 577 (K577M) in the recombinant human WRN protein.

Phenotype:

Model shows hypersensitivity to 4-nitroquinoline-1-oxide, reduced replicative potential, and reduced expression of the endogenous WRN protein.

Primary Citation:

lan wang, charles E. Ogburn, Carol B. Ware, Warren C. Ladiges, Hagop Youssoufian, George M. Martin, and Junko Oshima.  Celular Werner Phenotypes in Mice Expressing a Putative Dominant-Negative Human WRN Gene.  Genetics (2000) 154:357 – 362.

Medline Accession # 10628995

 

Tcrb- Vα8.2 Overexpression Model
  MMRRC Strain ID: 0131-H/M

This mouse model provides understanding of autoimmunity and intervention therapy.  Specifically, this is a model for rheumatoid arthritis.

Genotype:

Rearrangement of Vα11.1 and Vα8.2 TCR chain genes isolated from a T-cell hybridoma specific for CII using an internal promoter.

Phenotype:

Rapid onset of arthritis with sever clinical signs was detected in transgenic mice after immunization with CII in complete Freund’s adjuvant.  Histological analysis of inflamed joints resemble arthritic human joints.

 

Primary Citation:

Osman GE, Cheunsuk S, Allen SE, Chi E, Liggitt HD, Hood LE, Ladiges WC.  Expression of a type II collagen-specific TCR transgene accelerates the onset of arthritis in mice.  International Immunology (1998). 10(11): 1613 – 1622.

Medline Accession # 9846690

 

Mouse Models Under DevelopmentThe following mouse models are currently under development by the Mutant Mouse Regional Resource Centers (MMRRC) and not yet ready for distribution.  Please contact Heather Hopkins at hhopkins@u.washington.edu to request a mouse line directly from our laboratory.

  • P58IPK Deletion Model
Primary Citation: Ladiges W, Knoblaugh S, Sopher B, Korth M, MacAuley A, Goodman A, LeBoeuf R, Katze M. Pancreatic ß cell failure and diabetes in mice with a deletion mutation of the endoplasmic reticulum stress response gene P58IPK.  Diabetes, In Review.

 

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