EXCEEDTHE SPACE PROVIDED. One of the long term goals of this laboratory is to develop genetically-based strategies for the treatment of sickle cell anemia and p-thalassemia. The goal of this study is to determine whether homologous recombination can be developed as a strategy to repair mutant P-globin genes in embryonic stem cells and primary hematopoietic progenitors. To accomplish these goals, we propose the following specific aims.
Specific Aim 1 : We wi^ll_de_veTl_op_m^ice with a m. utation similar to the 3' filobin mui tation of humans by creating a mutation in the rnouse IJ-mapr globin gene using homologous recombination in embryonic stem cells. We will create embryonic stem cell lines that contain a mutation that causes an alanineMsoleucine substitution in position 6 of the murine p-major globin gene (P6I), and that have a selectable marker cassette (PGK-neo) either retained or excised (via Cre-Lox mediated recombination) downstream from p-major. These ES cells will be the starting material for Specific Aim 2, and will be used to make mice that bear the mutations. The hematopoietic cells of heterozygous mice with p6I (and the excised PGK-neo cassette) form the starting material for Specific Aim 3.
Specific Aim 2 : We will define the efficiency of homologous recombination-mediated repair of the P6 mutation in embryonic stem cells using targeting vectors of different sizes. To explore the relationship of targeting arm size and homologous recombination efficiency, we will create targeting vectors that contain a total of 8, 16, 60, or 110 kb of wild-type targeting DNA from the mouse p-globin cluster, and compare the abilities of these vectors to correct the p6I mutation in ES cells via homologous recombination.
Specific Aim 3 : We will determine whether hematopoietic progenitors have the ability to correct the |36I mutation via homologous recombinatien, using the targeting vectors defined in Specific Aim 2. Functional targeting vectors defined in Specific A:.m 2 will be used to determine whether hematopoietic progenitors and/or stem cells have the machinery to perform homologous recombination events within the p-globin locus. Bone marrow cells purified from mice heterozygous for the P6I mutation (and PGK-neo deleted) will be transfected with the targeting vectors using physical means of DNA delivery (i.e. electroporation or lipofection). These cells will be selected using either neomycin phosphotransferase or GFP expression (or both), and individual colonies derived from hematopoietic progenitors (LTC-IC and CFU-C) will be analyzed for the frequency of correction of the P6I mutation using PCR-based techniques. These studies should allow us to determine whether homologous recombination can be rationally developed as a method for correcting mutations in the P-globin locus within primary hematopoietic progenitor cells. PERFORMANCE SITE ========================================Section End===========================================
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