We propose to develop a gel based approach that would display most of the single base substitution mutations present in any mRNA expressed in a cell type. The method would permit recovery of bands for sequencing and identification of the sites of mutation. We describe the application of this approach to the detection of somatic mutations in malignant cells. In Phase 2 we propose to apply the method to malignant melanomas, colon carcinoma, acute Myelocytic leukemia and myelodysplasia. In addition, we propose protocols for improving the sensitivity of the method, for extending it to small tissue samples, and for detecting mutations in a small fraction of cells in a sample.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants Phase II (R33)
Project #
5R33CA088326-04
Application #
6633853
Study Section
Special Emphasis Panel (ZCA1-SRRB-C (M1))
Program Officer
Couch, Jennifer A
Project Start
2000-07-06
Project End
2004-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
4
Fiscal Year
2003
Total Cost
$512,242
Indirect Cost
Name
Yale University
Department
Genetics
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Pan, Xinghua; Weissman, Sherman M (2002) An approach for global scanning of single nucleotide variations. Proc Natl Acad Sci U S A 99:9346-51