Journal article
Molecular determinants and signaling effects of PKA RIα phase separation
Molecular cell, Vol.84(8), pp.1570-1584.e7
04/2024
DOI: 10.1016/j.molcel.2024.03.002
PMCID: PMC11031308
PMID: 38537638
Abstract
Spatiotemporal regulation of intracellular signaling molecules, such as the 3′,5′-cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA), ensures proper cellular function. Liquid-liquid phase separation (LLPS) of the ubiquitous PKA regulatory subunit RIα promotes cAMP compartmentation and signaling specificity. However, the molecular determinants of RIα LLPS remain unclear. Here, we reveal that two separate dimerization interfaces, combined with the cAMP-induced unleashing of the PKA catalytic subunit (PKA-C) from the pseudosubstrate inhibitory sequence, drive RIα condensate formation in the cytosol of mammalian cells, which is antagonized by docking to A-kinase anchoring proteins. Strikingly, we find that the RIα pseudosubstrate region is critically involved in forming a non-canonical R:C complex, which recruits active PKA-C to RIα condensates to maintain low basal PKA activity in the cytosol. Our results suggest that RIα LLPS not only facilitates cAMP compartmentation but also spatially restrains active PKA-C, thus highlighting the functional versatility of biomolecular condensates in driving signaling specificity.
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•RIα LLPS involves dimerization via two interfaces and cAMP-driven unleashing of PKA-C•Spatial PKA signaling is distinctly regulated by LLPS and AKAP anchoring•A non-canonical, active PKA holoenzyme exists in RIα condensates•RIα condensates retain active PKA-C to maintain low-cytosolic PKA signaling
Proper intracellular signaling is critical for cell health and function. Hardy et al. investigate how cells organize the activity architecture of PKA, a crucial cell signaling enzyme, revealing a non-canonical interaction that allows RIα biomolecular condensates to suppress cytosolic PKA activity and prevent aberrant signaling.
Details
- Title: Subtitle
- Molecular determinants and signaling effects of PKA RIα phase separation
- Creators
- Julia C. Hardy - University of California, San DiegoEmily H. Pool - University of California, San DiegoJessica G.H. Bruystens - University of California, San DiegoXin Zhou - University of California, San DiegoQingrong Li - University of California, San DiegoDaojia R. Zhou - University of California, San DiegoMax Palay - University of California, San DiegoGerald Tan - University of California, San DiegoLisa Chen - University of California, San DiegoJaclyn L.C. Choi - University of California, San DiegoHa Neul Lee - University of California, San DiegoStefan Strack - University of IowaDong Wang - University of California, San DiegoSusan S. Taylor - University of California, San DiegoSohum Mehta - University of California, San DiegoJin Zhang - University of California, San Diego
- Resource Type
- Journal article
- Publication Details
- Molecular cell, Vol.84(8), pp.1570-1584.e7
- Publisher
- Elsevier Inc
- DOI
- 10.1016/j.molcel.2024.03.002
- PMID
- 38537638
- PMCID
- PMC11031308
- ISSN
- 1097-2765
- eISSN
- 1097-4164
- Grant note
- DOI: 10.13039/100000002, name: National Institutes of Health; DOI: 10.13039/100007909, name: Fibrolamellar Cancer Foundation
- Language
- English
- Electronic publication date
- 03/22/2024
- Date published
- 04/2024
- Academic Unit
- Pathology; Iowa Neuroscience Institute; Fraternal Order of Eagles Diabetes Research Center; Neuroscience and Pharmacology
- Record Identifier
- 9984581221702771
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