BBS Faculty Member - Keith Blackwell

Keith Blackwell

Department of Genetics

Joslin Diabetes Center
One Joslin Place, Rm. 655B
Boston, MA 02215
Tel: 617-309-2760
Fax: 617-309-3403
Lab Members: 6 postdoctoral fellows

My lab studies how organisms defend against environmental and metabolic stresses, and how these stress defenses influence aging. Most of our work involves the nematode C. elegans as a model organism, and many of our projects are centered on the transcription regulator SKN-1/Nrf, which orchestrates a conserved response to oxidative stress and reactive toxins. SKN-1/Nrf activates detoxification genes and is required for oxidative stress resistance, and plays a central role in various mechanisms that extend healthy lifespan. Our recent work has implicated SKN-1/Nrf in a surprisingly broad spectrum of stress defense and homeostasis functions, including maintenance of proteasome function, the extracellular matrix, ER homeostasis, and lipid metabolism. One important goal is to elucidate how signals and cooperating factors modulate SKN-1/Nrf function so it can perform such a wide variety of functions. Another is to understand the involvement of these protective processes in determining lifespan.

We also want to understand how stress response factors such as SKN-1/Nrf are regulated in response to different stress and metabolic stimuli. We have found that SKN-1/Nrf is inhibited directly by insulin/IGF-1 signaling (IIS), and is important for the increased stress-resistance and longevity seen when IIS is reduced. We have also determined that SKN-1/Nrf responds to perturbations in protein synthesis, and is critical in relationships between growth signals, protein synthesis, and aging. This is particularly important in the context of the mTOR (mechanistic Target of Rapamycin) signaling pathways, which are central to growth regulation. More recently, we have identified a novel mode of redox-based signaling that regulates SKN-1 and other fundamental cellular regulators, and is evolutionarily conserved. We are applying the advantages of
C. elegans to expand our understanding of how SKN-1/Nrf proteins function and promote longevity, and of mechanisms through which they and other stress defenses are regulated under normal and adverse conditions.

Last Update: 1/22/2016


For a complete listing of publications click here.



Tullet JMA, Hertweck M, An JH, Baker J, Hwang JY, Liu S, Oliveira RP, Baumeister R, Blackwell TK. (2008) Direct inhibition of the longevity promoting factor SKN-1 by insulin-like signaling in C. elegans. Cell, 132, 1025-1038.

Robida-Stubbs S, Glover-Cutter C, Lamming DW, Mizunuma M, Narasimhan SD, Neumann-Haefelin E, Sabatini DM, Blackwell TK. (2012) TOR signaling and rapamycin influence longevity by regulating SKN-1/Nrf and DAF-16/FoxO.
Cell Metabolism, 15, 713-724.

Glover-Cutter KM, Lin S, Blackwell TK. (2013) Integration of the unfolded protein and oxidative stress responses through SKN-1/Nrf.
PLoS Genet., 9, e1003071.

Ewald CY, Landis JN, Porter Abate J. Murphy CT, Blackwell TK. (2015) Dauer-independent insulin/IGF-1 signalling implicates collagen remodelling in longevity.
Nature, 519, 97-101.

Steinbaugh MJ, Narasimhan SD, Robida-Stubbs S, Moronetti Mazzeo L, Dreyfuss JM, Hourihan JM, Raghavan P, Operana T, Esmaille, R, Blackwell TK. (2015) Lipid-mediated regulation of SKN-1/Nrf in response to germ cell absence.
eLife, advance publication.

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of Harvard College