Dual and dynamic intracellular localization of Arabidopsis thaliana SnRK1.1

J Exp Bot. 2019 Apr 15;70(8):2325-2338. doi: 10.1093/jxb/erz023.

Abstract

Sucrose non-fermenting 1 (SNF1)-related protein kinase 1.1 (SnRK1.1; also known as KIN10 or SnRK1α) has been identified as the catalytic subunit of the complex SnRK1, the Arabidopsis thaliana homologue of a central integrator of energy and stress signalling in eukaryotes dubbed AMPK/Snf1/SnRK1. A nuclear localization of SnRK1.1 has been previously described and is in line with its function as an integrator of energy and stress signals. Here, using two biological models (Nicotiana benthamiana and Arabidopsis thaliana), native regulatory sequences, different microscopy techniques, and manipulations of cellular energy status, it was found that SnRK1.1 is localized dynamically between the nucleus and endoplasmic reticulum (ER). This distribution was confirmed at a spatial and temporal level by co-localization studies with two different fluorescent ER markers, one of them being the SnRK1.1 phosphorylation target HMGR. The ER and nuclear localization displayed a dynamic behaviour in response to perturbations of the plastidic electron transport chain. These results suggest that an ER-associated SnRK1.1 fraction might be sensing the cellular energy status, being a point of crosstalk with other ER stress regulatory pathways.

Keywords: Nicotiana benthamiana; Arabidopsis; ER localization; SnRK1.1; chloroplast; dual localization; endoplasmic reticulum (ER); energy status; nuclear localization, retrograde signalling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / cytology
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / metabolism*
  • Cell Nucleus / metabolism*
  • Chloroplasts / metabolism
  • Electron Transport
  • Endoplasmic Reticulum / metabolism*
  • Energy Metabolism
  • Hydroxymethylglutaryl-CoA-Reductases, NADP-dependent / metabolism
  • Microscopy, Confocal
  • Microscopy, Fluorescence
  • Nicotiana / cytology
  • Nicotiana / metabolism
  • Plants, Genetically Modified / cytology
  • Plants, Genetically Modified / metabolism
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction / physiology
  • Stress, Physiological
  • Transcription Factors / metabolism

Substances

  • Arabidopsis Proteins
  • Transcription Factors
  • HMGR protein, Arabidopsis
  • Hydroxymethylglutaryl-CoA-Reductases, NADP-dependent
  • Protein Serine-Threonine Kinases
  • SnRK1 protein, Arabidopsis