CRISPR-Cas is a powerful molecular tool for changing the code of life. Jennifer Doudna and her team focus on developing novel CRISPR-Cas technologies and using them to study molecular mechanisms of disease. Their goal is to establish first-of-their-kind approaches to treat disease by cutting out or modifying harmful DNA.

Current research in Doudna’s lab focuses on discovering and characterizing novel CRISPR-Cas-related proteins, developing genome-editing tools for use in vitro and in vivo, and using CRISPR technology to better understand the genetics of certain cancers like glioblastoma. New discoveries in this field continue at a rapid pace, revealing a technology that has widespread applications.

Disease Areas

Infectious Diseases
Neurodegenerative Diseases

Areas of Expertise

Biochemistry and Structural Biology
CRISPR and Genome Editing

Lab Focus

Elucidating the mechanisms underlying CRISPR–Cas immunity in bacterial cells, especially the functions of the various Cas proteins discovered so far.
Developing and applying novel CRISPR-based tools toward applications in biotechnology, diagnostics, neurodegenerative diseases, and other diseases.
Understanding the mechanisms controlling translation—the reading of messenger RNAs (mRNAs) into proteins—with a focus on factors that regulate mRNA accessibility and on the inhibition of pathogens’ RNA translation by interferon during infection.

Research Impact

Doudna and her colleagues rocked the research world in 2012 by describing a simple way of editing the DNA of any organism using an RNA-guided protein found in bacteria. This technology, called CRISPR-Cas9, has opened the floodgates of possibility for human and non-human applications of gene editing, including assisting researchers in the fight against HIV, sickle cell disease, and muscular dystrophy. While it was possible to modify cells’ genomes prior to CRISPR-Cas9, this platform has revolutionized genetic engineering by its simplicity, versatility, and precision. Doudna’s lab continues to refine the technology by investigating the mechanisms of action of various bacterial Cas proteins, with an eye to adapting their findings toward specific applications in biotechnology or medicine.


Professional Titles

Senior Investigator, Gladstone Institutes

Investigator, Howard Hughes Medical Institute

Professor, Molecular and Cell Biology and Chemistry, UC Berkeley

Li Ka Shing Chancellor’s Chair in Biomedical and Health Sciences, UC Berkeley

Executive Director, Innovative Genomics Institute

Faculty Scientist, Physical Biosciences Division, Lawrence Berkeley National Laboratory


Jennifer Doudna is the Li Ka Shing Chancellor’s Chair and a professor in the Departments of Chemistry and of Molecular and Cell Biology at UC Berkeley, as well as an investigator of the Howard Hughes Medical Institute. Her co-discovery of CRISPR-Cas9 genetic engineering technology, with collaborator, French scientist Emmanuelle Charpentier, has changed human and agricultural genomics research forever. This genome-editing technology enables scientists to change or remove genes quickly, with a precision only dreamed of just a few years ago. Labs worldwide have re-directed the course of their research programs to incorporate this new tool, creating a CRISPR revolution with huge implications across biology and medicine. In addition to her scientific achievements and eminence, Doudna is also a leader in public discussion of the ethical and other implications of genome editing for human biology and societies, and advocates for thoughtful approaches to the development of policies around the use of CRISPR-Cas9. She has received many prizes for her discoveries, including the Japan Prize (2016), the Kavli Prize (2018), and the LUI Che Woo Welfare Betterment Prize (2019). In 2015, Doudna was named by Time magazine as one of the 100 most influential people in the world.

How Did You Get Your Start in Science?

“As a young student, my father got me a copy of the book, The Double Helix by James Watson. This telling of the mystery and discovery of science captured my imagination.”

Jennifer , PhD

Honors and Awards

2020 Wolf Prize in Medicine, The Wolf Foundation

2019 Microbiology Society Prize Medal, Scotland

2019 Harvey Prize, Technion, Israel

2019 Nierenberg Prize, Scripps Oceanographic Institute

2019 Lui Che Woo Welfare Betterment Prize

2018 Honorary Doctorate of Science, University of Southern California

2018 American Cancer Society Medal of Honor

2018 Kavli Prize in Nanoscience, Norway

2018 V de Vida Award, Spain

2018 Croonian Medal, Royal Society

2018 National Academy of Sciences Award in Chemical Sciences

2018 Gustavus John Esselen Award for Chemistry, Northeastern Sec Amer Chemical Society

2018 Lila & Murray Gruber Memorial Cancer Research Award, American Academy of Dermatology

2018 Dickson Prize in Science, Carnegie Mellon University

2018 Pearl Meister Greengard Prize, Rockefeller University

2017 Honorary Doctorate of Science, Hong Kong University

2017 Honorary Doctorate of Science, Mount Sinai School of Medicine

2017 Genius 100 Award, Canada

2017 George R. Stibitz Computer & Communications Pioneer Award

2017 The Edward O. Wilson Biodiversity Technology Pioneer Award

2017 Golden Plate Award, International Achievement Organization

2017 Albert Einstein Foundation Award

2017 Wallace H. Coulter Lectureship Award, The American Association for Clinical Chemistry

2017 Albany Medical Center Prize

2017 BBVA Frontiers of Knowledge Award, Spain

2017 F.A. Cotton Medal, The Texas A&M Section of the American Chemical Society

2017 The Japan Prize, Japan Prize Foundation

2017 Luminary Award, Precision Medicine World Conference

2017 Fellow, American Association for Cancer Research

2016 Honorary Doctorate of Science, Yale University

2016 Honorary Doctorate of Science, York University

2016 Heineken Prize, Netherlands

2016 Tang Prize in Biopharmaceutical Science, Taiwan

2016 Paul Allen Distinguished Investigator

2016 Canada Gairdner Prize, Canada

2016 Warren Alpert Foundation Prize, Harvard Medical School

2016 Nakasone Award, Human Frontier Science Program

2016 Paul Ehrlich and Ludwig Darmstaedter Prize, Germany

2016 L’Oreal-UNESCO International Prize for Women in Science

2015 Honorary Doctorate of Science, University of Leuven

2015 Association of Biomolecular Resource Facilities Award

2015 Charles Butcher Award, University of Colorado

2015 Massry Prize, UCLA/USC

2015 Gruber Prize in Genetics

2015 Princess of Asturias Award for Technical and Scientific Research

2015 International Society for Transgenic Technologies Prize

2015 Time 100, Time Magazine’s 100 most influential people in the world

2015 Fellow, American Society for Microbiology

2014 Breakthrough Prize in Life Sciences

2014 Member, National Academy of Inventors

2014 Foreign Policy’s 100 Leading Global Thinkers

2014 Jacob Heskel Gabbay Award in Biotechnology and Medicine

2014 Dr. Paul Janssen Award for Biomedical Research

2014 Member, National Academy of Inventors

2014 Lurie Prize, Foundation for the NIH

2013 BayBio Pantheon Award

2013 Hans Neurath Award, Protein Society

2013 Mildred Cohn Award, ASBMB

2010 Member, National Academy of Medicine

2008 Fellow, American Association for the Advancement of Science

2007 The Nucleic Acid Group Award, NACON VII, Sheffield, UK

2003 Member, American Academy of Arts and Sciences

2002 Member, National Academy of Sciences

2000 Eli Lilly Award in Biological Chemistry, American Chemical Society

2000 Jean Francois LeFevre Memorial Lectureship, CNRS, Strasbourg, France

2000 R.B. Woodward Visiting Professorship, Harvard University

2000 Alan T. Waterman Award, National Science Foundation

1999 National Academy of Sciences Award for Initiatives in Research

1996 Johnson Foundation Prize for Innovative Research


    • CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity. Chen, J.S., Ma, E., Harrington, L.B., Da Costa, M., Tian, X., Palefsky, J.M., and Doudna, J.A. (2018) Science 360, 436-439.
    • A broad-spectrum inhibitor of CRISPR-Cas9. Harrington, L.B., Doxzen, K.W., Ma, E., Liu, J., Knott, G.J., Edraki, A., Amrani, N., Chen, J.S., Cofsky, J.C., Kranzusch, P.J., Sontheimer, E.J., Davidson, A.R., Maxwell, K.L. and Doudna, J.A. (2017) Cell 170, 1224-1233.e15.
    • Structures of the CRISPR genome integration complex. Wright, A.V., Liu, J.J., Knott, G.J., Doxzen, K.W., Nogales, E. and Doudna, J.A. (2017) Science 357, 1113-1118.
    • Programmable RNA tracking in live cells with CRISPR-Cas9. Nelles, D.A., Fang, M.Y., O'Connell, M.R., Xu, J.L., Markmiller, S.J., Doudna, J.A. and Yeo, G.W. (2016) . Cell 65, 488-496.
    • Foreign DNA capture during CRISPR-Cas adaptive immunity. Nuñez, J.K., Harrington, L.B., Kranzusch, P.J., Engelman, A. and Doudna, J.A. (2015) Nature 527, 535-8.
    • Conformational control of DNA target cleavage by CRISPR-Cas9. Sternberg, S.H., LaFrance, B., Kaplan, M. and Doudna, J.A. (2015) Nature 527,110-113.
    • A Cas9-guide RNA complex pre-organized for target DNA recognition. Jiang, F., Zhou, K., Ma, K., Gressel, S. and Doudna, J.A. (2015) Science 348,1477-81.
    • Programmable RNA recognition and cleavage by CRISPR/Cas9. O’Connell, M.R., Oakes, B.L., Sternberg, S.H., East-Seletsky, A., Kaplan, M. and Doudna, J.A. (2014) Nature 516, 263-6.
    • Structures of Cas9 endonucleases reveal RNA-mediated conformational activation. Jinek, M., Jiang, F., Taylor, D.W., Sternberg, S.H., Kaya, E., Ma, E., Anders, C., Hauer, M., Zhou, K., Lin, S., Kaplan, M., Iavarone, A.T., Charpentier, E., Nogales, E. and Doudna, J.A. (2014) Science 343, 1247997.
    • DNA interrogation by the CRISPR RNA-guided endonuclease Cas9. Sternberg, S.H., Redding, S., Jinek, M.J., Greene, E.C. and Doudna, J.A. (2014) Nature 507, 62-7. (cover article; Perspective in Science published May 2014).
    • Heritable genome editing using TALENs and CRISPR/Cas9 to engineer precise insertions and deletions in evolutionarily diverse nematode species. Lo, T.W., Pickle, C.S., Lin, S., Ralston, E.J., Gurling, M., Schartner, C.M., Bian, Q., Doudna, J.A. and Meyer, B.J. (2013) Genetics 195, 331-48.
    • High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity. Pattanayak, V., Lin, S., Guilinger, J.P., Ma, E., Doudna, J.A. and Liu, D.R. (2013) Nature Biotechnol. 31, 839-43.
    • CRISPR mediated modular RNA-guided regulation of transcription in eukaryotes. Gilbert, L.A., Larson, M.H., Morsut, L., Liu, Z., Brar, G.A., Torres, S.E., Stern-Ginossar, N., Brandman, 8 O., Whitehead, E.H., Doudna, J.A., Lim, W.A., Weissman, J.S. and Qi, L.S. (2013) Cell 154, 442-51.
    • Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression. Qi LS, Larson MH, Gilbert LA, Doudna JA, Weissman JS, Arkin AP, Lim WA. (2013) Cell 152, 1173-83.
    • RNA-programmed genome editing in human cells. Jinek, M., East, A., Cheng, A., Ma, E. and Doudna, J.A. (2013) eLife 2, e00471.
    • A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity. Jinek, M., Chylinski, K., Fonfara, I., Hauer, M., *Doudna, J.A. and *Charpentier E. (2012) Science 337, 816-21.  *corresponding authors
    • Structures of the RNA-guided surveillance complex from a bacterial immune system. Wiedenheft, B., Lander, G.C., Zhou, K., Jore, M.M., Brouns, S.J., van der Oost, J., Doudna, J.A. and Nogales, E. (2011) Nature 477, 486-9.
    • An RNA-induced conformational change required for CRISPR RNA cleavage by the endoribonuclease Cse3. Sashital, D.G., Jinek, M. and Doudna, J.A. (2011) Nature Struct. Mol. Biol. 18, 680-7. PMID: 21572442.
    • RNA-guided complex from a bacterial immune system enhances target recognition through seed sequence interactions. Wiedenheft, B., van Duijn, E., Bultema, J., Waghmare, S., Zhou, K., Barendregt, A., Westphal, W., Heck, A., Boekema, E., Dickman, M. and Doudna, J.A. (2011) Proc. Natl. Acad. Sci. USA 108, 10092-7.
    • Structural basis for CRISPR RNA-guided DNA recognition by Cascade. Jore, M.M., Lundgren, M., van Duijn, E., Bultema, J.B., Westra, E.R., Waghmare, S.P., Wiedenheft, B., Pul, U., Wurm, R., Wagner, R., Beijer, M.R., Barendregt, A., Zhou, K., Snijders, A.P., Dickman, M.J., Doudna, J.A., Boekema, E.J., Heck, A.J., van der Oost, J., Brouns, S.J. (2011) Nature Struct. Mol. Biol. 18, 529- 36. 
    • Structural basis for CRISPR RNA-guided DNA recognition by Cascade. Haurwitz, R.E., Jinek, M., Wiedenheft, B., Zhou, K. and Doudna, J.A. (2010) Sequence- and structurespecific RNA processing by a CRISPR endonuclease. Science 329, 1355-8.

More Publications




Senior Executive Assistant

Lab Members

Alexandra , PhD
Visiting Postdoc
Rotation Student
Muhammad Abdullah , PhD
Postdoctoral Scholar
I-Li , PhD
Postdoctoral Scholar
Research Associate I