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.mRNA localization | mRNA sorting | green RNA | porin | plant E ukaryotic cells are characterized by compartmentalization of functions in complex organelles, and cell activity depends on synthesis and precise localization of proteins. The mechanisms of protein sorting are the subject of intense research, and models are often reevaluated (1). The earliest models for protein localization were based on the presence of targeting signals in the polypeptide sequences. However, the targeting of mRNAs to various subcellular regions has recently emerged as an essential regulatory step for protein localization (2).Mitochondria contain hundreds of proteins, but only a few are encoded by the mitochondrial genome. The other proteins are nucleus-encoded and imported into the organelle. Protein import into mitochondria is controlled by peptide sequences that are recognized by mitochondrial receptors (3, 4). In parallel with this posttranslational model, a cotranslational model is now emerging (2, 5). A microarray analysis in Saccharomyces cerevisiae has shown that approximately half of the mRNAs encoding mitochondrial proteins are found in the vicinity of mitochondria (6). Mitochondrial targeting of mRNA was also demonstrated in mammals and plants (7,8).Mechanisms of mitochondrial targeting of mRNAs were essentially studied in yeast. In this species, three factors have been clearly identified to influence mRNA targeting to the mitochondrial surface. (i) Targeting of many but not all mRNAs appears dependent on translation (9, 10). (ii) The RNA-binding protein Puf3p is essential for mitochondrial targeting of a subset of mRNAs (9). (iii) The translocase of the outer mitochondrial membrane (TOM complex) is also involved in mRNA binding (10-12). In addition, some mRNAs are...