Isoform-specific subcellular localization and function of protein kinase A identified by mosaic imaging of mouse brain

Author:

Ilouz Ronit1,Lev-Ram Varda1,Bushong Eric A2ORCID,Stiles Travis L3,Friedmann-Morvinski Dinorah45,Douglas Christopher3,Goldberg Jeffrey L3,Ellisman Mark H26,Taylor Susan S17ORCID

Affiliation:

1. Department of Pharmacology, University of California, San Diego, La Jolla, United States

2. Center for Research in Biological Systems, National Center for Microscopy and Imaging Research, University of California, San Diego, San Diego, United States

3. Department of Ophthalmology, Shiley Eye Center, University of California, San Diego, La Jolla, United States

4. Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, United States

5. Department of Biochemistry and Molecular Biology, George S Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel

6. Department of Neurosciences, University of California, San Diego School of Medicine, La Jolla, United States

7. Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, United States

Abstract

Protein kinase A (PKA) plays critical roles in neuronal function that are mediated by different regulatory (R) subunits. Deficiency in either the RIβ or the RIIβ subunit results in distinct neuronal phenotypes. Although RIβ contributes to synaptic plasticity, it is the least studied isoform. Using isoform-specific antibodies, we generated high-resolution large-scale immunohistochemical mosaic images of mouse brain that provided global views of several brain regions, including the hippocampus and cerebellum. The isoforms concentrate in discrete brain regions, and we were able to zoom-in to show distinct patterns of subcellular localization. RIβ is enriched in dendrites and co-localizes with MAP2, whereas RIIβ is concentrated in axons. Using correlated light and electron microscopy, we confirmed the mitochondrial and nuclear localization of RIβ in cultured neurons. To show the functional significance of nuclear localization, we demonstrated that downregulation of RIβ, but not of RIIβ, decreased CREB phosphorylation. Our study reveals how PKA isoform specificity is defined by precise localization.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of General Medical Sciences

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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