Abstract

Aminoacyl-tRNA synthetases (AaRS) charge tRNAs with amino acids for protein translation. In plants, cytoplasmic, mitochondrial, and chloroplast AaRS exist that are all coded for by nuclear genes and must be imported from the cytosol. In addition, only a few of the mitochondrial tRNAs needed for translation are encoded in mitochondrial DNA. Despite considerable progress made over the last few years, still little is known how the bulk of cytosolic AaRS and respective tRNAs are transported into mitochondria. Here, we report the identification of a protein complex that ties AaRS and tRNA import into the mitochondria of Arabidopsis thaliana. Using leucyl-tRNA synthetase 2 (LeuRS2) as a model for a mitochondrial signal peptide (MSP)-less precursor, a ≈30 kDa protein was identified that interacts with LeuRS2 during import. The protein identified is identical with a previously characterized mitochondrial protein designated HP30-2 (encoded by At3g49560) that contains a sterile alpha motif (SAM) similar to that found in RNA binding proteins. HP30-2 is part of a larger protein complex that contains with TIM22, TIM8, TIM9 and TIM10 four previously identified components of the translocase for MSP-less precursors. Lack of HP30-2 perturbed mitochondrial biogenesis and function and caused seedling lethality during greening, suggesting an essential role of HP30-2 in planta.

Highlights

  • Arabidopsis Mitochondria pLeuRS1 and leucyl-tRNA synthetase 2 (LeuRS2) are distinct gene products in Arabidopsis; pLeuRS1 is encoded by At4g04350 and LeuRS2 is encoded by At1g09620

  • LeuRS2 and LeuRS1 share the presence of conserved HIGH and KMSKS motives in the catalytic site and the presence of an editing domain comprising conserved Threonine-rich and GTG motives needed for high-fidelity aminoacylation of tRNA (Figure S1)

  • These results indicated that the NH2 -terminal mitochondrial signal peptide (MSP) and tRNA-binding domain (TRBD) differentially regulated mitochondrial protein import

Read more

Summary

Introduction

Aminoacyl-tRNA synthetases (AaRS) play important roles in all eukaryotic cells [1]. It has been reported that many cytoplasmic and mitochondrial AaRS activities are encoded by distinct nuclear genes [2]. Single nuclear genes encode both, cytoplasmic and mitochondrial AaRS isoforms. An example is provided by yeast valyl-tRNA synthetase (ValRS) [7]. Studies showed that both ValRS isoforms accomplish non-redundant roles and could not substitute for each other in vivo [7]. Chiu et al [8] examined the evolutionary basis of converting a bacterial tRNA synthetase into a yeast cytoplasmic or mitochondrial enzyme and identified an NH2 -terminal appendage comprising a MSP and a nonspecific tRNA-binding domain (TRBD) that act in cis and rendered the bacterial enzyme functional both in the cytoplasm and in mitochondria

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call