A-kinase-interacting protein localizes protein kinase A in the nucleus

Proc Natl Acad Sci U S A. 2005 Jan 11;102(2):349-54. doi: 10.1073/pnas.0408608102. Epub 2005 Jan 3.

Abstract

The genetic variability and covalent modifications associated with the amino terminus of the protein kinase A (PKA) catalytic (C) subunit suggest that it may contribute to protein-protein interactions and/or localization. By using a yeast two-hybrid screen, we identified a PKA-interacting protein (AKIP1) that binds to the amino terminus (residues 1-39) of the C subunit of PKA. The interaction was localized to the A helix (residues 14-39) of the C subunit and to the carboxyl terminus of AKIP1. AKIP1 thus defines the amino-terminal A helix of PKA as a protein interaction motif. In normal breast (Hs 578 Bst) and HeLa cells, AKIP1 is present in the nucleus as speckles. A nuclear localization signal (Arg-14 and Arg-15) was identified. Upon stimulation with forskolin, HeLa cells expressing AKIP1 accumulated higher levels of the endogenous C subunit in the nucleus. Deletion of the carboxyl terminus of AKIP1 or overexpression of residues 1-39 of the C subunit abolished nuclear localization of the activated endogenous C subunit. Thus, AKIP1 describes a PKA-interacting protein that can contribute to localization by a mechanism that is distinct from A-kinase anchoring proteins that interact with the regulatory subunits.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Active Transport, Cell Nucleus*
  • Amino Acid Sequence
  • Animals
  • Cyclic AMP-Dependent Protein Kinases / chemistry
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Mice
  • Molecular Sequence Data
  • Nuclear Proteins / analysis
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / physiology*
  • Protein Subunits
  • Protein Transport
  • Proteins

Substances

  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Protein Subunits
  • Proteins
  • aryl hydrocarbon receptor-interacting protein
  • Cyclic AMP-Dependent Protein Kinases