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Heads of Laboratories

Jeremy M. Rock, Ph.D.
Assistant Professor
Laboratory of Host-Pathogen Biology

Mycobacterium tuberculosis is the leading cause of death due to infectious disease and infects one-third of the world’s population. By investigating the mechanisms that enable this bacterium to cause tuberculosis and evade current antibiotics, the Rock lab aims to lay the foundation for new therapeutic strategies to improve control of this pandemic.

Despite the discovery of effective antibiotics, tuberculosis (TB) remains an enduring global public health threat. New drugs, drug regimens, and innovative approaches to limit drug resistance are desperately needed—and to facilitate their development, the Rock lab seeks to provide a more complete understanding of the genetic and biochemical basis of Mycobacterium tuberculosis (Mtb) pathogenesis.

Genetic studies of this bacterium have thus far been hampered by the difficulties associated with conventional genetic tools. To fill this methodological gap, Rock and colleagues developed a CRISPR interference (CRISPRi) gene knockdown method for Mtb. This transformative tool will enable the systematic interrogation of gene function in Mtb using high-throughput approaches to previously intractable problems in the field. The Rock lab uses this and other methods to study, among other things, the mechanisms that enable chronic infection, antibiotic tolerance and resistance, and large-scale genetic and chemical interactions.

TB is a chronic, progressive disease, often with a long period of latency following initial infection. In most cases, the host immune system is capable of restraining but not eliminating Mtb, leading to lifelong infection. The mechanisms that enable the pathogen to persist in the face of a robust adaptive immune response, sometimes for decades, are incompletely understood. The Rock lab is using new approaches to define the genetic basis for persistent Mtb infection.

Mtb infection can be treated with antibiotics. However, effective TB treatment requires a combination of four drugs taken for a minimum of six months. This lengthy treatment, necessitated by the presence of antibiotic-tolerant bacilli that arise during infection, is one of the most important roadblocks to effective TB control. Moreover, antibiotic tolerance can ultimately facilitate the evolution of antibiotic resistance, thereby fueling the growing problem of drug-resistant TB. As a postdoctoral fellow, Rock discovered an ancient mechanism of DNA replication proofreading in Mtb that is central to controlling the drug-resistance rate. His lab is currently investigating the molecular mechanisms of antibiotic tolerance, as well as the mechanisms by which the bacterium can ultimately evolve antibiotic resistance.

Finally, the lab is interested in using genome-scale genetic and chemical interaction mapping to improve Mtb chemotherapy. The current four-drug combination to treat TB was developed in the 1960s. Rock seeks to identify new antibiotic combinations that leverage drug target synergies to create more potent antibiotic regimens, thereby reducing treatment time and limiting the emergence of drug resistance.

Jeremy Rock will join Rockefeller effective January 1, 2018.


EDUCATION

B.A. in biochemistry and economics, 2004
University of California, Berkeley

Ph.D. in biology, 2012
Massachusetts Institute of Technology

POSTDOC

Harvard School of Public Health, 2012–2017

POSITIONS

Research Associate, 2004–2006
Sangamo Biosciences

Assistant Professor, 2018–
The Rockefeller University

SELECTED PUBLICATIONS

Rock J.M. et al. Programmable transcriptional repression in mycobacteria using an orthogonal CRISPR interference platform. Nat. Microbiol 2, 16274 (2017).

Rock J.M. et al. DNA replication fidelity in Mycobacterium tuberculosis is mediated by an ancestral prokaryotic proofreader. Nat. Genet. 47, 677–681 (2015).

Rock J.M. et al. Activation of the yeast Hippo pathway by phosphorylation-dependent assembly of signaling complexes. Science 340, 871–875 (2013).

Rock J.M. et al. Cdc15 integrates Tem1 GTPase-mediated spatial signals with polo kinase-mediated temporal cues to activate mitotic exit. Genes Dev. 25, 1943–1954 (2011).

Urnov F. et al. Highly efficient endogenous human gene correction using designed zinc-finger nucleases. Nature 435, 646–651 (2005).