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Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology
Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology
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Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology
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Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology
Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology

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Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology
Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology
Journal Article

Differential targeting of VDAC3 mRNA isoforms influences mitochondria morphology

2014
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Overview
Intracellular targeting of mRNAs has recently emerged as a prevalent mechanism to control protein localization. For mitochondria, a cotranslational model of protein import is now proposed in parallel to the conventional posttranslational model, and mitochondrial targeting of mRNAs has been demonstrated in various organisms. Voltage-dependent anion channels (VDACs) are the most abundant proteins in the outer mitochondrial membrane and the major transport pathway for numerous metabolites. Four nucleus-encoded VDACs have been identified in Arabidopsis thaliana . Alternative cleavage and polyadenylation generate two VDAC3 mRNA isoforms differing by their 3′ UTR. By using quantitative RT-PCR and in vivo mRNA visualization approaches, the two mRNA variants were shown differentially associated with mitochondria. The longest mRNA presents a 3′ extension named alternative UTR (aUTR) that is necessary and sufficient to target VDAC3 mRNA to the mitochondrial surface. Moreover, aUTR is sufficient for the mitochondrial targeting of a reporter transcript, and can be used as a tool to target an unrelated mRNA to the mitochondrial surface. Finally, VDAC3–aUTR mRNA variant impacts mitochondria morphology and size, demonstrating the role of mRNA targeting in mitochondria biogenesis.