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

Integrase-mediated spacer acquisition during CRISPR-Cas adaptive immunity.
Authors: Authors: Nuñez JK, Lee AS, Engelman A, Doudna JA.
Nature
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Structure-guided reprogramming of human cGAS dinucleotide linkage specificity.
Authors: Authors: Kranzusch PJ, Lee ASY, Wilson SC, Solovykh MS, Vance RE, Berger JM, Doudna JA.
Cell
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A genome-wide small interfering RNA screen identifies host factors required for vesicular stomatitis virus infection.
Authors: Authors: Lee AS, Burdeinick-Kerr R, Whelan SP.
J Virol
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Structure of human cGAS reveals a conserved family of second-messenger enzymes in innate immunity.
Authors: Authors: Kranzusch PJ, Lee AS, Berger JM, Doudna JA.
Cell Rep
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A ribosome-specialized translation initiation pathway is required for cap-dependent translation of vesicular stomatitis virus mRNAs.
Authors: Authors: Lee AS, Burdeinick-Kerr R, Whelan SP.
Proc Natl Acad Sci U S A
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Construction and manipulation of a new Kaposi's sarcoma-associated herpesvirus bacterial artificial chromosome clone.
Authors: Authors: Brulois KF, Chang H, Lee AS, Ensser A, Wong LY, Toth Z, Lee SH, Lee HR, Myoung J, Ganem D, Oh TK, Kim JF, Gao SJ, Jung JU.
J Virol
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Peroxisomes are signaling platforms for antiviral innate immunity.
Authors: Authors: Dixit E, Boulant S, Zhang Y, Lee AS, Odendall C, Shum B, Hacohen N, Chen ZJ, Whelan SP, Fransen M, Nibert ML, Superti-Furga G, Kagan JC.
Cell
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Helicobacter hepaticus urease is not required for intestinal colonization but promotes hepatic inflammation in male A/JCr mice.
Authors: Authors: Ge Z, Lee A, Whary MT, Rogers AB, Maurer KJ, Taylor NS, Schauer DB, Fox JG.
Microb Pathog
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Receptor determinants of zoonotic transmission of New World hemorrhagic fever arenaviruses.
Authors: Authors: Radoshitzky SR, Kuhn JH, Spiropoulou CF, Albariño CG, Nguyen DP, Salazar-Bravo J, Dorfman T, Lee AS, Wang E, Ross SR, Choe H, Farzan M.
Proc Natl Acad Sci U S A
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Bacterial cytolethal distending toxin promotes the development of dysplasia in a model of microbially induced hepatocarcinogenesis.
Authors: Authors: Ge Z, Rogers AB, Feng Y, Lee A, Xu S, Taylor NS, Fox JG.
Cell Microbiol
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