Yali Dou

Professor of Medicine and Cancer Biology

Marion and Harry Keiper Chair in Cancer Research

Co-Director of the Ph.D. Program in Molecular Medicine

Co-Director of the USC Norris Brown Center for Cancer Drug Development

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Overview

Dr. Yali Dou is a Professor in the Department of Medicine and Department of Biochemistry and Molecular Medicine. She is Marion and Harry Keiper Endowed Professor for cancer research. Dr. Dou is the Associate Director for Basic Science at Norris Comprehensive Cancer Center.

Dr. Dou has received a number of prestigious awards including the Leukemia & Lymphoma Society Scholar Award (2012), Stand Up to Cancer IRG Award (2011), AACR Gertrude B. Elion Cancer Research Award (2010) and Dean’s Award in Basic Science at University of Michigan (2014). Dr. Dou was selected to AAAS Fellow in 2025.

Research Interests
Cell fate decisions are controlled by transcription factors acting in concert with epigenetic regulators, which include enzymes that carry out histone post-translational modifications. Epigenetic mechanism underlies cell fate commitment and plasticity; its dysregulation emerges as a key characteristic of human malignancies. The Dou lab uses multidisciplinary approaches to study the establishment and maintenance of gene regulatory networks, focusing on how chromatin modifications exert temporal and spatial gene regulation via transcription factors and DNA regulatory elements. The lab is also interested in the interplays between chromatin modifications and other important cellular processes, including metabolic regulation, genome stability and higher order chromatin organization. In particular, Dou lab has extensive research on the MLL/KMT2 family of histone methyltransferases. MLL/KMT2 deposit histone H3 lysine 4 methylation, which prominently marks active gene promoters and distal enhancers. The MLL/KMT2 enzymes are frequently deleted, mutated or translocated in acute leukemia, solid tumors as well as a wide spectrum of human developmental syndromes. The study will not only advance understanding of the fundamental roles of epigenetic modulators in development and diseases, but also provide critical insights into designing novel target-based therapeutic strategies for cancer treatment and regenerative medicine.

Awards

  • AAAS Fellow, 2025
  • Co-organizer, FASEB conference on Biology of Acetylation in Human Diseases, 2024
  • 2023
     -: Chair, NIH Cancer Genetics (CG) study section, 2023
     – 2025
  • Marion and Harry Keiper Chair in Cancer Research, 2021
  • Dean’s Award in Basic Science, University of Michigan, 2014
  • UMMS League of Research Excellence, University of Michigan, 2014
  • 2012
     -: Leukemia & Lymphoma Society Scholar Award, 2012
     – 2017
  • Stand Up to Cancer IRG Award, 2011
  • American Cancer Society RSG Award, 2010
  • AACR Gertrude B. Elion Cancer Research Award, 2010
  • Biomedical Science Scholar, University of Michigan, 2007
  • 2004
     -: The Irvington Institute for Immunological Research Fellowship, 2004
     – 2007

Research Funding

  • Defining the role of RNA binding by the MLL1 (KMT2A) complex in leukemia
    NIH · R01CA310146 · Jul 1, 2026 – Jun 30, 2031 · Role: Co-Principal Investigator
  • Reversible Biological Acetylation in Health and Disease
    NIH · R13CA290701 · Aug 1, 2024 – Jul 31, 2025 · Role: Principal Investigator
  • Non-canonical function of transcription cofactor MLL1 in cancer
    NIH · R01CA287625 · Feb 1, 2024 – Jan 31, 2029 · Role: Principal Investigator
  • Structural insights into the MLL core complexes
    NIH · R01CA250329 · Aug 25, 2020 – May 31, 2025 · Role: Principal Investigator
  • Enhancer Dysregulation in AML
    NIH · R01CA232263 · Mar 1, 2019 – Feb 28, 2025 · Role: Principal Investigator
  • PRDM16 function in neural development
    NIH · R01NS100156 · Sep 1, 2016 – Aug 31, 2021 · Role: Principal Investigator
  • Chromatin replication control by protein ubiquitylation
    NIH · R21CA190911 · Aug 7, 2015 – Jul 31, 2017 · Role: Principal Investigator
  • Targeting MLL3 histone methyltransferase
    NIH · R01CA187004 · Apr 15, 2015 – Mar 31, 2018 · Role: Principal Investigator
  • Cytokine-induced epigenetic changes during chronic lung disease
    NIH · R01HL112897 · Jun 15, 2013 – May 31, 2017 · Role: Co-Principal Investigator
  • Targeting the MLL-WDR5 protein-protein interaction
    NIH · R01CA177307 · Apr 9, 2013 – Mar 31, 2018 · Role: Co-Principal Investigator
  • Function of MLL in transcription regulation
    NIH · R01GM082856 · Apr 1, 2009 – Apr 30, 2025 · Role: Principal Investigator

Publications

  • Dysregulation of intercellular signaling by MOF deletion leads to liver injury. J Biol Chem. 2021 Jan-Jun; 296:100235.. View in PubMed
  • Histone Acetyltransferase MOF Blocks Acquisition of Quiescence in Ground-State ESCs through Activating Fatty Acid Oxidation. Cell Stem Cell. 2020 09 03; 27(3):441-458.e10.. View in PubMed
  • Cryo-EM structure of the human MLL1 core complex bound to the nucleosome. Nat Commun. 2019 12 05; 10(1):5540.. View in PubMed
  • HOXA9 Reprograms the Enhancer Landscape to Promote Leukemogenesis. Cancer Cell. 2018 10 08; 34(4):643-658.e5.. View in PubMed
  • MLL1 Inhibition Reprograms Epiblast Stem Cells to Naive Pluripotency. Cell Stem Cell. 2016 Apr 07; 18(4):481-94.. View in PubMed
  • Hijacked in cancer: the KMT2 (MLL) family of methyltransferases. Nat Rev Cancer. 2015 Jun; 15(6):334-46.. View in PubMed
  • Targeting MLL1 H3K4 methyltransferase activity in mixed-lineage leukemia. Mol Cell. 2014 Jan 23; 53(2):247-61.. View in PubMed
  • The histone acetyltransferase MOF is a key regulator of the embryonic stem cell core transcriptional network. Cell Stem Cell. 2012 Aug 03; 11(2):163-78.. View in PubMed