A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation

PLoS One. 2014 Mar 28;9(3):e93255. doi: 10.1371/journal.pone.0093255. eCollection 2014.

Abstract

Introduction: Phosphatidylinositol-4,5-bisphosphate (PIP2) is a cofactor necessary for the activity of KCNQ1 channels. Some Long QT mutations of KCNQ1, including R243H, R539W and R555C have been shown to decrease KCNQ1 interaction with PIP2. A previous study suggested that R539W is paradoxically less sensitive to intracellular magnesium inhibition than the WT channel, despite a decreased interaction with PIP2. In the present study, we confirm this peculiar behavior of R539W and suggest a molecular mechanism underlying it.

Methods and results: COS-7 cells were transfected with WT or mutated KCNE1-KCNQ1 channel, and patch-clamp recordings were performed in giant-patch, permeabilized-patch or ruptured-patch configuration. Similar to other channels with a decreased PIP2 affinity, we observed that the R243H and R555C mutations lead to an accelerated current rundown when membrane PIP2 levels are decreasing. As opposed to R243H and R555C mutants, R539W is not more but rather less sensitive to PIP2 decrease than the WT channel. A molecular model of a fragment of the KCNQ1 C-terminus and the membrane bilayer suggested that a potential novel interaction of R539W with cholesterol stabilizes the channel opening and hence prevents rundown upon PIP2 depletion. We then carried out the same rundown experiments under cholesterol depletion and observed an accelerated R539W rundown that is consistent with this model.

Conclusions: We show for the first time that a mutation may shift the channel interaction with PIP2 to a preference for cholesterol. This de novo interaction wanes the sensitivity to PIP2 variations, showing that a mutated channel with a decreased affinity to PIP2 could paradoxically present a slowed current rundown compared to the WT channel. This suggests that caution is required when using measurements of current rundown as an indicator to compare WT and mutant channel PIP2 sensitivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arrhythmias, Cardiac / genetics
  • Arrhythmias, Cardiac / metabolism
  • Brugada Syndrome
  • COS Cells
  • Cardiac Conduction System Disease
  • Cell Line
  • Chlorocebus aethiops
  • Cholesterol / genetics
  • Cholesterol / metabolism*
  • Heart Conduction System / abnormalities
  • Heart Conduction System / metabolism
  • KCNQ1 Potassium Channel / genetics
  • KCNQ1 Potassium Channel / metabolism*
  • Long QT Syndrome / genetics*
  • Long QT Syndrome / metabolism
  • Magnesium / metabolism
  • Mutation / genetics*
  • Phosphatidylinositol 4,5-Diphosphate / genetics
  • Phosphatidylinositol 4,5-Diphosphate / metabolism*

Substances

  • KCNQ1 Potassium Channel
  • Phosphatidylinositol 4,5-Diphosphate
  • Cholesterol
  • Magnesium

Grants and funding

This work was supported by the Agence Nationale de la Recherche (ANR-05-JCJC-0160-01), the AFMTéléthon, and a Marie Curie International Outgoing Fellowship within the 7th European Community Framework Programme (GL). FCC and FA-A were recipients of a grant from the French Ministère de la Recherche. FA-A was supported by the Fondation d'entreprise Genavie. JP was supported by the Association Française contre les Myopathies. CSN was supported by the INSERM (poste d'accueil). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.