Abstract

The mitochondrial transcriptome from land plants undergoes hundreds of specific C-to-U changes by RNA editing. These events are important since most of them occur in the coding region of mRNAs. One challenging question is to understand the mechanism of recognition of a selected C residue (editing sites) on the transcript. It has been reported that a short region surrounding the target C forms the cis-recognition elements, but individual residues on it do not play similar roles for the different editing sites. Here, we studied the role of the −1 and +1 nucleotide in wheat cox2 editing site recognition using an in organello approach. We found that four different recognition patterns can be distinguished: (a) +1 dependency, (b) −1 dependency, (c) +1/−1 dependency, and (d) no dependency on nearest neighbor residues. A striking observation was that whereas a 23 nt cis region is necessary for editing, some mutants affect the editing efficiency of unmodified distant sites. As a rule, mutations or pre-edited variants of the transcript have an impact on the complete set of editing targets. When some Cs were changed into Us, the remaining editing sites presented a higher efficiency of C-to-U conversion than in wild type mRNA. Our data suggest that the complex response observed for cox2 mRNA may be a consequence of the fate of the transcript during mitochondrial gene expression.

Highlights

  • RNA editing challenges the central dogma of molecular biology as it changes the information encoded for by the gene at the RNA level

  • While around 30 editing events occur in the chloroplast transcriptome [3], more than 400 cytosine residues are changed to uracil in flowering plant mitochondria [4,5,6,7,8]

  • After introduction of the recombinant DNA into T. aestivum mitochondria, the mRNA was analyzed by RT-PCR and the identity of spliced molecules was verified by sequence analysis

Read more

Summary

Introduction

RNA editing challenges the central dogma of molecular biology as it changes the information encoded for by the gene at the RNA level. This process affects a wide variety of organisms through nucleotide insertion/deletion or nucleotide conversion [1]. RNA editing occurs by site-specific deamination of cytosines [2]. While around 30 editing events occur in the chloroplast transcriptome [3], more than 400 cytosine residues are changed to uracil in flowering plant mitochondria [4,5,6,7,8]. RNA editing constitutes an essential step to ensure the production of functional proteins and the proper functioning of mitochondria [9,10]

Methods
Results
Conclusion
Full Text
Published version (Free)

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