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Regulation of nuclear PKA revealed by spatiotemporal manipulation of cyclic AMP

Nature Chemical Biology volume 8, pages 375382 (2012) | Download Citation

  • A Corrigendum to this article was published on 20 May 2013


Understanding how specific cyclic AMP (cAMP) signals are organized and relayed to their effectors in different compartments of the cell to achieve functional specificity requires molecular tools that allow precise manipulation of cAMP in these compartments. Here we characterize a new method using bicarbonate-activatable and genetically targetable soluble adenylyl cyclase to control the location, kinetics and magnitude of the cAMP signal. Using this live-cell cAMP manipulation in conjunction with fluorescence imaging and mechanistic modeling, we uncovered the activation of a resident pool of protein kinase A (PKA) holoenzyme in the nuclei of HEK-293 cells, modifying the existing dogma of cAMP-PKA signaling in the nucleus. Furthermore, we show that phosphodiesterases and A-kinase anchoring proteins (AKAPs) are critical in shaping nuclear PKA responses. Collectively, our data suggest a new model in which AKAP-localized phosphodiesterases tune an activation threshold for nuclear PKA holoenzyme, thereby converting spatially distinct second messenger signals to temporally controlled nuclear kinase activity.

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Change history

  • Corrected online 19 April 2013

    In the version of this article initially published, the domain schemes in Figure 1a were incorrectly labeled sACt (aa 1–146). The correct text is sACt (aa 1–469). The error has been corrected in the HTML and PDF versions of the article.


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We thank L. Levin (Weill Cornell Medical College, Cornell University) for the gift of sACt cDNA. We thank M. Houslay (Institute of Biomedical and Life Sciences, University of Glasgow) and K. Xiang (University of Illinois, Urbana-Champaign) for the gift of dnPDE4 isoforms. We thank L. Hersh (University of Kentucky College of Medicine) for giving us the A126.1B2 and A126.1B2 Catβ cell line. We also thank S. Mehta, G. Mo, T. Ueno, C. Pohlmeyer and T. Inoue for their technical help. This work was funded by US National Institutes of Health (NIH) grants R01 DK073368, DP1 OD006419 (to J.Z.), F31 DK074381 (to L.M.D.) and R01 HL094476, American Heart Association grant 0830470N (to J.J.S.) and NIH grant GM08715 (to J.H.Y.).

Author information

Author notes

    • Vedangi Sample
    • , Lisa M DiPilato
    •  & Jason H Yang

    These authors contributed equally to this work.


  1. Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

    • Vedangi Sample
    • , Lisa M DiPilato
    • , Qiang Ni
    •  & Jin Zhang
  2. Department of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.

    • Jason H Yang
    •  & Jeffrey J Saucerman
  3. Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

    • Jin Zhang
  4. Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

    • Jin Zhang


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Q.N. conceived the original idea for SMICUS. V.S., L.M.D., Q.N. and J.Z. designed the experimental aspects of the project. J.H.Y. and J.J.S. designed the modeling aspects of the project. V.S. and L.M.D. carried out the experiments. J.H.Y. developed the mathematical model and carried out the simulations. V.S., L.M.D., J.H.Y., Q.N., J.J.S. and J.Z. analyzed the data. J.Z., L.M.D., V.S. and J.H.Y. wrote the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding authors

Correspondence to Jeffrey J Saucerman or Jin Zhang.

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