Epigenetic Regulation
The focus of my research is to investigate the molecular mechanisms governing Ikaros-mediated transcriptional regulation of vasoactive intestinal peptide receptor - 1 (VPACR-1) in T lymphocytes. Ikaros is a master regulator of lymphopoiesis and sets the threshold for T cell activation. Ikaros mutated mouse models develop an aggressive lymphoblastic leukemia with 100% incidence. Some human leukemias express mutated dominant negative Ikaros isoforms that inhibit full-length Ikaros DNA binding. Decreases in Ikaros binding capacity may downregulate a subset of genes capable of regulating T cell proliferation. Recently, we demonstrated that the gene for VPACR-1, a G protein coupled, anti-proliferative receptor expressed on naive T cells, is a novel gene target for Ikaros. Signaling through the anti-proliferative VPACR-1 protein may naturally impede cell cycle entry in CD4 T cells. Therefore, a decrease in Ikaros protein and/or DNA binding capacity, during certain etiologies of lymphoblastic leukemia, may downregulate VPACR-1 and contribute to uncontrolled proliferation. Understanding how Ikaros regulates VPACR-1 in naive and actiavted CD4 T cells may
- provide insight into a crucial downstream event from Ikaros that contributes to uncontrolled proliferation in hematopoietic disorders and
- lead to an understanding of the role Ikaros-mediated regulation of VPACR-1 plays in normal immune function, such as suppressing bystander T cell activation in certain organs including the gastrointestinal system.
Therefore, the aims of my research will be to
- confirm bi-directional effects of Ikaros on VPACR-1 expression in primary naive and actiavted CD4 T lymphocytes
- demonstrate which PKC pathway signaling proteins mediate TCR-dependant VPACR-1 downregulation, and
- identify IK phosphoacceptor residues that mediate Ikaros recruitment to heterochromatin during T cell activation.








Graduate programs in Chemistry and Biochemistry 