Alternative splicing-mediated targeting of the Arabidopsis GLUTAMATE RECEPTOR3.5 to mitochondria affects organelle morphology.
Enrico TeardoLuca CarrarettoSara De BortoliAlex CostaSmrutisanjita BeheraRichard WagnerFiorella Lo SchiavoElide FormentinIldiko SzaboPublished in: Plant physiology (2014)
Since the discovery of 20 genes encoding for putative ionotropic glutamate receptors in the Arabidopsis (Arabidopsis thaliana) genome, there has been considerable interest in uncovering their physiological functions. For many of these receptors, neither their channel formation and/or physiological roles nor their localization within the plant cells is known. Here, we provide, to our knowledge, new information about in vivo protein localization and give insight into the biological roles of the so-far uncharacterized Arabidopsis GLUTAMATE RECEPTOR3.5 (AtGLR3.5), a member of subfamily 3 of plant glutamate receptors. Using the pGREAT vector designed for the expression of fusion proteins in plants, we show that a splicing variant of AtGLR3.5 targets the inner mitochondrial membrane, while the other variant localizes to chloroplasts. Mitochondria of knockout or silenced plants showed a strikingly altered ultrastructure, lack of cristae, and swelling. Furthermore, using a genetically encoded mitochondria-targeted calcium probe, we measured a slightly reduced mitochondrial calcium uptake capacity in the knockout mutant. These observations indicate a functional expression of AtGLR3.5 in this organelle. Furthermore, AtGLR3.5-less mutant plants undergo anticipated senescence. Our data thus represent, to our knowledge, the first evidence of splicing-regulated organellar targeting of a plant ion channel and identify the first cation channel in plant mitochondria from a molecular point of view.
Keyphrases
- cell wall
- transcription factor
- cell death
- arabidopsis thaliana
- poor prognosis
- plant growth
- endoplasmic reticulum
- binding protein
- reactive oxygen species
- cancer therapy
- healthcare
- oxidative stress
- wild type
- induced apoptosis
- cell cycle arrest
- genome wide
- small molecule
- endothelial cells
- electronic health record
- drug delivery
- ionic liquid
- quantum dots
- high throughput
- cell proliferation
- gene expression
- amino acid
- machine learning