All three research projects in this Program depend very heavily on the use of a facility which can successfully and efficiently produce transgenic mice by conventional means and mutant animals by homologous recombination in embryonic stem cells. The director proposes to establish a gene manipulation Core built on an existing transgenic/ES cell facility at Caltech. The facility will be responsible for producing genetically engineered animals and will serve as a common central repository from which unmodified animals can be obtained. A centralized cell culture facility will be established to standardize the necessary set of techniques needed to produce animals with inactivated genes. This facility will serve as a producer of mutant cell lines (and animals) and also serve as a training resource for individuals who wish to learn and master this technology. To preserve transgenic mice and animals with targeted gene mutations, a cryopreservation facility is proposed.

Project Start
1998-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
5
Fiscal Year
1999
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Louie, A Y; Huber, M M; Ahrens, E T et al. (2000) In vivo visualization of gene expression using magnetic resonance imaging. Nat Biotechnol 18:321-5
Studer, L; Csete, M; Lee, S H et al. (2000) Enhanced proliferation, survival, and dopaminergic differentiation of CNS precursors in lowered oxygen. J Neurosci 20:7377-83
Zabludoff, S D; Csete, M; Wagner, R et al. (1998) p27Kip1 is expressed transiently in developing myotomes and enhances myogenesis. Cell Growth Differ 9:1-11
Zinyk, D L; Mercer, E H; Harris, E et al. (1998) Fate mapping of the mouse midbrain-hindbrain constriction using a site-specific recombination system. Curr Biol 8:665-8
Yoon, J K; Olson, E N; Arnold, H H et al. (1997) Different MRF4 knockout alleles differentially disrupt Myf-5 expression: cis-regulatory interactions at the MRF4/Myf-5 locus. Dev Biol 188:349-62
Cornelison, D D; Wold, B J (1997) Single-cell analysis of regulatory gene expression in quiescent and activated mouse skeletal muscle satellite cells. Dev Biol 191:270-83
Zabludoff, S D; Wright, W W; Harshman, K et al. (1996) BRCA1 mRNA is expressed highly during meiosis and spermiogenesis but not during mitosis of male germ cells. Oncogene 13:649-53
Patapoutian, A; Yoon, J K; Miner, J H et al. (1995) Disruption of the mouse MRF4 gene identifies multiple waves of myogenesis in the myotome. Development 121:3347-58