PKA phosphorylation of HERG protein regulates the rate of channel synthesis

Am J Physiol Heart Circ Physiol. 2009 May;296(5):H1244-54. doi: 10.1152/ajpheart.01252.2008. Epub 2009 Feb 20.

Abstract

Acute changes in cAMP and protein kinase A (PKA) signaling can regulate ion channel protein activities such as gating. Effects on channels due to chronic PKA signaling, as in stress or disease states, are less understood. We examined the effects of prolonged PKA activity on the human ether-a-go-go-related gene (HERG) K(+) channel in stably transfected human embryonic kidney (HEK)293 cells. Sustained elevation of cAMP by either chlorophenylthiol (CPT)-cAMP or forskolin increased the HERG channel protein abundance two- to fourfold within 24 h, with measurable difference as early as 4 h. The cAMP-induced augmentation was not due to changes in transcription and was specific for HERG compared with other cardiac K(+) channels (Kv1.4, Kv1.5, Kir2.1, and KvLQT1). PKA activity was necessary for the effect on HERG protein and did not involve other cAMP signaling pathways. Direct PKA phosphorylation of the HERG protein was responsible for the cAMP-induced augmentation. Enhanced abundance of HERG protein was detected in endoplasmic reticulum-enriched, Golgi, and plasma membrane without significant changes in trafficking rates or patterns. An increase in the K(+) current density carried by the HERG channel was also observed, but with a delay, suggesting that traffic to the surface is rate-limiting traffic. Acceleration of the HERG protein synthesis rate was the primary factor in the cAMP/PKA effect with lesser effects on protein stability. These results provide evidence for a novel mechanism whereby phosphorylation of a nascent protein dictates its rate of synthesis, resetting its steady-state abundance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Membrane / metabolism
  • Cells, Cultured
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • ERG1 Potassium Channel
  • Endoplasmic Reticulum / metabolism
  • Ether-A-Go-Go Potassium Channels / biosynthesis*
  • Ether-A-Go-Go Potassium Channels / drug effects
  • Ether-A-Go-Go Potassium Channels / genetics
  • Golgi Apparatus / metabolism
  • Heat-Shock Proteins / metabolism
  • Humans
  • Kinetics
  • Membrane Potentials
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / enzymology*
  • Phosphorylation
  • Potassium / metabolism
  • Protein Stability
  • Protein Transport
  • Rabbits
  • Signal Transduction* / drug effects
  • Thionucleotides / pharmacology
  • Transfection
  • Up-Regulation

Substances

  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • Heat-Shock Proteins
  • KCNH2 protein, human
  • Thionucleotides
  • Colforsin
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • Potassium