Ali Shilatifard

Shilatifard has said he developed his love of science as a young boy working with and observing his grandfather,[7] a physician/scientist and professor of medicine of the University of Tehran. Shilatifard moved to the United States in 1984 where he began his study of organic chemistry at Kennesaw State University in Georgia. He began to work on his doctoral degree in biochemistry at the University of Georgia, Athens. Shilatifard completed his Ph.D. from the University of Oklahoma where his mentor, Dr. Richard Cummings, had moved his program. As a Jane Coffin Childs Postdoctoral Fellow at the Oklahoma Medical Research Foundation, Shilatifard identified the first function of any of the MLL translocation partners found in leukemia[8] and proposed that transcriptional elongation control is central to leukemia pathogenesis. Shilatifard began his independent lab in the Edward A. Doisy Department of Biochemistry and Molecular Biology at the St. Louis University School of Medicine, where he identified the first histone H3 lysine 4 (H3K4) methylase in Saccharomyces cerevisiae: which he named Set1/COMPASS;[9][10] and defined the pathway of histone H3K4 methylation which is highly conserved from yeast to human.[11][12] Studies from Shilatifard’s laboratory linking epigenetic factors and transcription elongation control to malignancies have provided therapeutic approaches for the treatment of these cancers.[13][14][15] He also served on the Life Sciences jury for the Infosys Prize in 2017. On April 12, 2019, Shilatifard presented "Childhood Leukemia: On the Edge of Extinction!" at TEDxUofIChicago.[16]

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