The investigators have determined that the LTC-IC assays differ significantly between C57/BL-6, DBA-2 and BALB-c mice. Loci termed Scfr-1 and Scfr-2 are proposed and investigators will focus on positionally cloning these genes and their human homologs. They will do this by generating mouse backcrosses to localize the Scfr genes within 1 Mb fragments. These regions will then be used to evaluate overlapping arrays of yeast and bacterial artificial chromosomes. Definition of the Scfr genes will be based on several criteria such as cDNA selection and expression polymorphisms. In addition, the investigators will analyze which cells in the stem cell hierarchy and at which stages of development strain specific differences are seen and whether or not these are also identified in localized peripheral blood samples.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK052177-01A1
Application #
2391524
Study Section
Hematology Subcommittee 2 (HEM)
Program Officer
Badman, David G
Project Start
1997-09-01
Project End
1998-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Medical Biology Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Sieburg, Hans B; Cho, Rebecca H; Muller-Sieburg, Christa E (2002) Limiting dilution analysis for estimating the frequency of hematopoietic stem cells: uncertainty and significance. Exp Hematol 30:1436-43
Muller-Sieburg, C E; Cho, R H; Sieburg, H B et al. (2000) Genetic control of hematopoietic stem cell frequency in mice is mostly cell autonomous. Blood 95:2446-8