| Literature DB >> 27789739 |
Monika W Murcha1,2,3,4,5,6,7, Szymon Kubiszewski-Jakubiak8,9,10,11,12,13,14, Pedro F Teixeira8,9,10,11,12,13,14, Irene L Gügel8,9,10,11,12,13,14, Beata Kmiec8,9,10,11,12,13,14, Reena Narsai8,9,10,11,12,13,14, Aneta Ivanova8,9,10,11,12,13,14, Cyrille Megel8,9,10,11,12,13,14, Annette Schock8,9,10,11,12,13,14, Sabrina Kraus8,9,10,11,12,13,14, Oliver Berkowitz8,9,10,11,12,13,14, Elzbieta Glaser8,9,10,11,12,13,14, Katrin Philippar8,9,10,11,12,13,14, Laurence Maréchal-Drouard8,9,10,11,12,13,14, Jürgen Soll8,9,10,11,12,13,14, James Whelan1,2,3,4,5,6,7.
Abstract
A variety of eukaryotes, in particular plants, do not contain the required number of tRNAs to support the translation of mitochondria-encoded genes and thus need to import tRNAs from the cytosol. This study identified two Arabidopsis (Arabidopsis thaliana) proteins, Tric1 and Tric2 (for tRNA import component), which on simultaneous inactivation by T-DNA insertion lines displayed a severely delayed and chlorotic growth phenotype and significantly reduced tRNA import capacity into isolated mitochondria. The predicted tRNA-binding domain of Tric1 and Tric2, a sterile-α-motif at the C-terminal end of the protein, was required to restore tRNA uptake ability in mitochondria of complemented plants. The purified predicted tRNA-binding domain binds the T-arm of the tRNA for alanine with conserved lysine residues required for binding. T-DNA inactivation of both Tric proteins further resulted in an increase in the in vitro rate of in organello protein synthesis, which was mediated by a reorganization of the nuclear transcriptome, in particular of genes encoding a variety of proteins required for mitochondrial gene expression at both the transcriptional and translational levels. The characterization of Tric1/2 provides mechanistic insight into the process of tRNA import into mitochondria and supports the theory that the tRNA import pathway resulted from the repurposing of a preexisting protein import apparatus.Entities:
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Year: 2016 PMID: 27789739 PMCID: PMC5129730 DOI: 10.1104/pp.16.01519
Source DB: PubMed Journal: Plant Physiol ISSN: 0032-0889 Impact factor: 8.340