The proposed studies are directed at the molecular mechanisms responsible for the regulation of fetal hemoglobin (HbF) and adult hemoglobin (HbA) synthesis in the baboon. Our previous results have demonstrated that a reverse switch from the production of HbA to HbF occurs in baboons subjected to acute erythropoietic stress or treatment with the DNA hypomethylating agent, 5-azacytidine. This reverse switch also occurs in patients with sickle cell anemia and Beta thalassemia who are treated with 5-azacytidine. The clinical effect of increased HbF in these patients was promising, but possible carcinogenicity has hindered further studies. A better understanding of the molecular mechanisms responsible for HbF to HbA switching may indicate better approaches to therapy without producing intolerable side effects. Our studies focus on the role of non-histone nuclear proteins (DNA sequence-specific binding proteins) in controlling HbF expression during gestation. Nuclear proteins will be extracted from nucleated erythroid cells of pre- and post-switch baboon fetuses to determine whether differences in DNA-binding proteins exist in fetuses synthesizing HbF compared to animals synthesizing HbA. DNA binding will be examined using DNA fragments containing known globin gene regulatory sequences. We plan to test for the functional significance of these DNA- binding proteins by in vitro transcription assays, and to purify those proteins that participate in globin gene switching. The regulatory protein genes will be cloned for use in structure and function studies. These cDNA clones will also be used in transfection experiments to evaluate their therapeutic potential.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK040093-05
Application #
2141185
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1990-02-01
Project End
1996-01-31
Budget Start
1994-02-01
Budget End
1996-01-31
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Sengupta, P K; Lavelle, D; DeSimone, J (1994) Increased binding of Sp1 to the gamma-globin gene promoter upon site-specific cytosine methylation. Am J Hematol 46:169-72
Sengupta, P K; Lavelle, D E; DeSimone, J (1994) The 87-kD A gamma-globin enhancer-binding protein is a product of the HOXB2(HOX2H) locus. Blood 83:1420-7
Lavelle, D; DeSimone, J; Heller, P (1993) Fetal hemoglobin reactivation in baboon and man: a short perspective. Am J Hematol 42:91-5
Lavelle, D; Ducksworth, J; Eves, E et al. (1991) A homeodomain protein binds to gamma-globin gene regulatory sequences. Proc Natl Acad Sci U S A 88:7318-22