The long-term goal of this project is to understand the developmental and coordinate regulation of globin genes in erythroid cells. These studies provide therapeutic strategies for genetically inherited dysfunctions of erythroid cells such as thalassemias and sickle cell anemia. Previous efforts on this project culminated in the detailed comparison of alpha- like and beta-like globin gene clusters between rabbit and human that revealed several candidates for regulatory elements. (1) Despite the requirement to balance production of alpha- and beta-globins, their genes reside in radically different segments of the genome. The CpG islands encompassing the rabbit alpha-globin gene may form an enhancer- independent promoter, and this will be tested by measuring the levels of expression in cells transfected with a series of constructs varying size, number and composition of CpG islands, and by attempting to resurrect an inactive CpG island by addition of active 5' flanking sequences. The ability of fragments of the alpha-globin gene to serve as enhancers will be tested, sequence-specific binding proteins will be purified, and cDNA clones encoding them isolated to aid in structural characterization. These proteins will be compared with those enriched in the CpG-rich fraction of chromatin. (2) Strong regulatory elements located distally in the rabbit beta- and alpha-like globin gene clusters (called locus control regions) will be sequenced, compared to homologous regions in humans and other mammals, and tested for enhancer function, independence from position effects, impact on developmental control and scaffold attachment. (3) Finally, striking patterns of sequence matches are seen in comparisons of rabbit and human epsilon-globin genes and the enhancer located 3' to the beta-globin gene. These conserved sequences will be tested for ability to affect expression of linked reporter genes and to bind nuclear proteins specifically. Novel proteins will be purified and characterized.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK027635-12
Application #
3228418
Study Section
Molecular Biology Study Section (MBY)
Project Start
1980-12-01
Project End
1996-04-30
Budget Start
1992-05-15
Budget End
1993-04-30
Support Year
12
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Pennsylvania State University
Department
Type
Schools of Arts and Sciences
DUNS #
City
University Park
State
PA
Country
United States
Zip Code
16802
Tufarelli, Cristina; Hardison, Ross; Miller, Webb et al. (2004) Comparative analysis of the alpha-like globin clusters in mouse, rat, and human chromosomes indicates a mechanism underlying breaks in conserved synteny. Genome Res 14:623-30
Patrinos, George P; Giardine, Belinda; Riemer, Cathy et al. (2004) Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res 32:D537-41
Hardison, Ross C; Roskin, Krishna M; Yang, Shan et al. (2003) Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolution. Genome Res 13:13-26
Schwartz, Scott; Kent, W James; Smit, Arian et al. (2003) Human-mouse alignments with BLASTZ. Genome Res 13:103-7
Bulger, Michael; Schubeler, Dirk; Bender, M A et al. (2003) A complex chromatin landscape revealed by patterns of nuclease sensitivity and histone modification within the mouse beta-globin locus. Mol Cell Biol 23:5234-44
Frazer, Kelly A; Elnitski, Laura; Church, Deanna M et al. (2003) Cross-species sequence comparisons: a review of methods and available resources. Genome Res 13:1-12
Giardine, Belinda; Elnitski, Laura; Riemer, Cathy et al. (2003) GALA, a database for genomic sequence alignments and annotations. Genome Res 13:732-41
Hardison, R C; Chiaromonte, F; Kolbe, D et al. (2003) Global predictions and tests of erythroid regulatory regions. Cold Spring Harb Symp Quant Biol 68:335-44
Schwartz, Scott; Elnitski, Laura; Li, Mei et al. (2003) MultiPipMaker and supporting tools: Alignments and analysis of multiple genomic DNA sequences. Nucleic Acids Res 31:3518-24
Elnitski, Laura; Riemer, Cathy; Petrykowska, Hanna et al. (2002) PipTools: a computational toolkit to annotate and analyze pairwise comparisons of genomic sequences. Genomics 80:681-90

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