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Variations in efficiency of plastidial RNA editing within ndh transcripts of perennial ryegrass (Lolium perenne) are not linked to differences in drought tolerance

ABSTRACT: Projected climate change is likely to subject key temperate grassland species, such as perennial ryegrass (Lolium perenne) to drought stress. Previous studies have shown that the NADH dehydrogenase complex (NDH) is involved with countering oxidative stress during environmental stresses like drought. We studied RNA editing within plastidial transcripts of the NDH complex in relation to the drought response of several accessions of perennial ryegrass. We found dramatic and reproducible differences in RNA editing efficiency between accessions, but efficiency was not influenced by imposition of drought stress, and a direct relationship between editing behaviour and drought response was not detected. Maintenance of healthy grasslands is essential for efficient livestock production, yet projected climate change is likely to place a heavy drought stress burden on key grassland species, such as perennial ryegrass (Lolium perenne). It is therefore important to gather an in-depth knowledge of the underlying plant response to this stress. The present study is focused on RNA editing (post-transcriptional nucleotide modifications resulting in altered transcripts) within plastidial transcripts of the NADH:ubiquinone oxidoreductase (NDH) complex (NADH dehydrogenase complex) in relation to the drought response of several accessions of perennial ryegrass. Previous studies have shown that the NDH complex is involved in countering oxidative stress during environmental stresses like drought. Owing to the nature of RNA editing within this complex, the RNA editing machinery could play a potential role in regulating the activity of the NDH complex. The investigation revealed dramatic and reproducible differences in RNA editing efficiency between accessions, but efficiency was not influenced by imposition of drought stress, and a direct relationship between editing behaviour and drought response was not detected.

SUBMITTER: Van Den Bekerom R

PROVIDER: S-EPMC4455615 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Project description:BackgroundSingle nucleotide polymorphisms (SNPs) are increasingly becoming the DNA marker system of choice due to their prevalence in the genome and their ability to be used in highly multiplexed genotyping assays. Although needed in high numbers for genome-wide marker profiles and genomics-assisted breeding, a surprisingly low number of validated SNPs are currently available for perennial ryegrass.ResultsA perennial ryegrass unigene set representing 9,399 genes was used as a reference for the assembly of 802,156 high quality reads generated by 454 transcriptome sequencing and for in silico SNP discovery. Out of more than 15,433 SNPs in 1,778 unigenes fulfilling highly stringent assembly and detection parameters, a total of 768 SNP markers were selected for GoldenGate genotyping in 184 individuals of the perennial ryegrass mapping population VrnA, a population being previously evaluated for important agronomic traits. A total of 592 (77%) of the SNPs tested were successfully called with a cluster separation above 0.9. Of these, 509 (86%) genic SNP markers segregated in the VrnA mapping population, out of which 495 were assigned to map positions. The genetic linkage map presented here comprises a total of 838 DNA markers (767 gene-derived markers) and spans 750 centi Mogan (cM) with an average marker interval distance of less than 0.9 cM. Moreover, it locates 732 expressed genes involved in a broad range of molecular functions of different biological processes in the perennial ryegrass genome.ConclusionsHere, we present an efficient approach of using next generation sequencing (NGS) data for SNP discovery, and the successful design of a 768-plex Illumina GoldenGate genotyping assay in a complex genome. The ryegrass SNPs along with the corresponding transcribed sequences represent a milestone in the establishment of genetic and genomics resources available for this species and constitute a further step towards molecular breeding strategies. Moreover, the high density genetic linkage map predominantly based on gene-associated DNA markers provides an important tool for the assignment of candidate genes to quantitative trait loci (QTL), functional genomics and the integration of genetic and physical maps in perennial ryegrass, one of the most important temperate grassland species.

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Variations in efficiency of plastidial RNA editing within ndh transcripts of perennial ryegrass (Lolium perenne) are not linked to differences in drought tolerance

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