Amy Lee

Amy Lee, Ph.D.

Assistant Professor of Cancer Immunology and Virology (Dana-Farber Cancer Institute)
Assistant Professor of Cell Biology (HMS)

Amy S.Y. Lee, Ph.D. received her Ph.D. in Virology at Harvard University in 2012, and then performed postdoctoral research on biochemical and cellular mechanisms of gene regulation at University of California – Berkeley. She joined the faculty in the Department of Biology at Brandeis University in 2016, and subsequently moved to join Harvard Medical School and DFCI in 2020. 

The Lee Lab studies how cells sense and respond to environmental signals by modulating protein synthesis. Specifically, the lab’s research is focused on discovering mechanisms regulating specialized mRNA translation and how these pathways are controlled during organismal development, viral infection, and cellular stress. To obtain broad insights into regulation of protein synthesis, the Lee lab applies an integrative approach combining RNA-protein biochemistry, cell-based experiments, structural biology, and development of new sequencing-based technology. Our research provides mechanistic understanding of the translation regulation networks that coordinate the precise control required for correct development and cellular function.

Dana-Farber Cancer Institute

450 Brookline Ave., SM520A

Boston, MA, 02115

Lab telephone: 857-215-1339

A phosphorylation-regulated eIF3d translation switch mediates cellular adaptation to metabolic stress.
Authors: Authors: Lamper AM, Fleming RH, Ladd KM, Lee ASY.
Science
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CBASS Immunity Uses CARF-Related Effectors to Sense 3'-5'- and 2'-5'-Linked Cyclic Oligonucleotide Signals and Protect Bacteria from Phage Infection.
Authors: Authors: Lowey B, Whiteley AT, Keszei AFA, Morehouse BR, Mathews IT, Antine SP, Cabrera VJ, Kashin D, Niemann P, Jain M, Schwede F, Mekalanos JJ, Shao S, Lee ASY, Kranzusch PJ.
Cell
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A molecular filter for the cnidarian stinging response.
Authors: Authors: Weir K, Dupre C, van Giesen L, Lee AS, Bellono NW.
Elife
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A complex suite of loci and elements in eukaryotic type II topoisomerases determine selective sensitivity to distinct poisoning agents.
Authors: Authors: Blower TR, Bandak A, Lee ASY, Austin CA, Nitiss JL, Berger JM.
Nucleic Acids Res
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Repression of ferritin light chain translation by human eIF3.
Authors: Authors: Pulos-Holmes MC, Srole DN, Juarez MG, Lee AS, McSwiggen DT, Ingolia NT, Cate JH.
Elife
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Modular Architecture of the STING C-Terminal Tail Allows Interferon and NF-?B Signaling Adaptation.
Authors: Authors: de Oliveira Mann CC, Orzalli MH, King DS, Kagan JC, Lee ASY, Kranzusch PJ.
Cell Rep
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Bacterial cGAS-like enzymes synthesize diverse nucleotide signals.
Authors: Authors: Whiteley AT, Eaglesham JB, de Oliveira Mann CC, Morehouse BR, Lowey B, Nieminen EA, Danilchanka O, King DS, Lee ASY, Mekalanos JJ, Kranzusch PJ.
Nature
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eIF3d is an mRNA cap-binding protein that is required for specialized translation initiation.
Authors: Authors: Lee AS, Kranzusch PJ, Doudna JA, Cate JH.
Nature
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Ancient Origin of cGAS-STING Reveals Mechanism of Universal 2',3' cGAMP Signaling.
Authors: Authors: Kranzusch PJ, Wilson SC, Lee AS, Berger JM, Doudna JA, Vance RE.
Mol Cell
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eIF3 targets cell-proliferation messenger RNAs for translational activation or repression.
Authors: Authors: Lee AS, Kranzusch PJ, Cate JH.
Nature
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