Gene targeting provides the means for creating mice with designed modifications in any chosen gene. This technology permits the evaluation of the function of any gene in the living mouse and the systematic dissection of the most complex biological processes. It can be used to generate animal models of any human disease in order to study its pathology at a level of detail not feasible in human patients, and for the development of new more effective therapies that are based on a molecular-genetic understanding of the disease. This grant will continue to emphasize the development of gene-targeting-based technologies for the study of human biology and medicine. The particular projects that will be pursued in this grant proposal through the use of gene targeting include: To determine the roles of Hox genes in building simple neural circuits, particularly those involving the facial and lumbar motor nuclei; and to model the human sarcomas, alveolar rhabdomyosarcoma, synovial sarcoma, and Ewing's sarcoma in the mouse. These are very aggressive cancers that principally affect children, adolescents, and young adults and do not respond satisfactorily to the current common therapeutic modalities of surgery, radiation, and chemotherapy. They are prime candidates for the development of new, more effective therapies based on an understanding of the molecular etiology responsible for the progression of each of these cancers. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM021168-33A1
Application #
7315258
Study Section
Development - 2 Study Section (DEV2)
Program Officer
Haynes, Susan R
Project Start
1976-12-01
Project End
2011-07-31
Budget Start
2007-08-05
Budget End
2008-07-31
Support Year
33
Fiscal Year
2007
Total Cost
$397,897
Indirect Cost
Name
University of Utah
Department
Genetics
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Du, Xuguang; Feng, Tao; Yu, Dawei et al. (2015) Barriers for Deriving Transgene-Free Pig iPS Cells with Episomal Vectors. Stem Cells 33:3228-38
Haldar, Malay; Karan, Goutam; Watanabe, Shuichi et al. (2014) Response: Contributions of the Myf5-independent lineage to myogenesis. Dev Cell 31:539-41
Straessler, Krystal M; Jones, Kevin B; Hu, Hao et al. (2013) Modeling clear cell sarcomagenesis in the mouse: cell of origin differentiation state impacts tumor characteristics. Cancer Cell 23:215-27
Jones, Kevin B; Datar, Manasi; Ravichandran, Sandhya et al. (2013) Toward an understanding of the short bone phenotype associated with multiple osteochondromas. J Orthop Res 31:651-7
Jones, K B; Su, L; Jin, H et al. (2013) SS18-SSX2 and the mitochondrial apoptosis pathway in mouse and human synovial sarcomas. Oncogene 32:2365-71, 2375.e1-5
Su, Le; Sampaio, Arthur V; Jones, Kevin B et al. (2012) Deconstruction of the SS18-SSX fusion oncoprotein complex: insights into disease etiology and therapeutics. Cancer Cell 21:333-47
Makki, Nadja; Capecchi, Mario R (2012) Cardiovascular defects in a mouse model of HOXA1 syndrome. Hum Mol Genet 21:26-31
Yan, Kelley S; Chia, Luis A; Li, Xingnan et al. (2012) The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations. Proc Natl Acad Sci U S A 109:466-71
Rogers, Scott W; Tvrdik, Petr; Capecchi, Mario R et al. (2012) Prenatal ablation of nicotinic receptor alpha7 cell lineages produces lumbosacral spina bifida the severity of which is modified by choline and nicotine exposure. Am J Med Genet A 158A:1135-44
Boulet, Anne M; Capecchi, Mario R (2012) Signaling by FGF4 and FGF8 is required for axial elongation of the mouse embryo. Dev Biol 371:235-45

Showing the most recent 10 out of 18 publications