4.6 Article

A Phosphodiesterase 2A Isoform Localized to Mitochondria Regulates Respiration

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 286, Issue 35, Pages 30423-30432

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M111.266379

Keywords

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Funding

  1. National Institutes of Health [R01 GM088999, R01 GM62328, NS552555]
  2. Muscular Dystrophy Association
  3. United Mitochondrial Disease Foundation
  4. Deutsche Forschungsgemeinschaft
  5. Forschungsreferat Ruhr-Universitat Bochum Medizin [F630-2008]

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Mitochondria are central organelles in cellular energy metabolism, apoptosis, and aging processes. A signaling network regulating these functions was recently shown to include soluble adenylyl cyclase as a local source of the second messenger cAMP in the mitochondrial matrix. However, a mitochondrial cAMP degrading phosphodiesterase (PDE) necessary for switching off this cAMP signal has not yet been identified. Here, we describe the identification and characterization of a PDE2A isoform in mitochondria from rodent liver and brain. We find that mitochondrial PDE2A is located in the matrix and that the unique N terminus of PDE2A isoform 2 specifically leads to mitochondrial localization of this isoform. Functional assays show that mitochondrial PDE2A forms a local signaling system with soluble adenylyl cyclase in the matrix, which regulates the activity of the respiratory chain. Our findings complete a cAMP signaling cascade in mitochondria and have implications for understanding the regulation of mitochondrial processes and for their pharmacological modulation.

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