Identification and functional annotation of long intergenic non-coding RNAs in Brassicaceae

An extensive effort to identify and functionally annotate long intergenic noncoding RNAs in four plant species within the mustards, including Arabidopsis thaliana and Brassica rapa. Long intergenic noncoding RNAs (lincRNAs) are a large yet enigmatic class of eukaryotic transcripts that can have critical biological functions. The wealth of RNA-sequencing (RNA-seq) data available for plants provides the opportunity to implement a harmonized identification and annotation effort for lincRNAs that enables cross-species functional and genomic comparisons as well as prioritization of functional candidates. In this study, we processed >24 Tera base pairs of RNA-seq data from >16,000 experiments to identify similar to 130,000 lincRNAs in four Brassicaceae: Arabidopsis thaliana, Camelina sativa, Brassica rapa, and Eutrema salsugineum. We used nanopore RNA-seq, transcriptome-wide structural information, peptide data, and epigenomic data to characterize these lincRNAs and identify conserved motifs. We then used comparative genomic and transcriptomic approaches to highlight lincRNAs in our data set with sequence or transcriptional conservation. Finally, we used guilt-by-association analyses to assign putative functions to lincRNAs within our data set. We tested this approach on a subset of lincRNAs associated with germination and seed development, observing germination defects for Arabidopsis lines harboring T-DNA insertions at these loci. LincRNAs with Brassicaceae-conserved putative miRNA binding motifs, small open reading frames, or abiotic-stress modulated expression are a few of the annotations that will guide functional analyses into this cryptic portion of the transcriptome.

Automated summary

In this study, the researchers identified and functionally annotated long intergenic noncoding RNAs (lincRNAs) in four plant species. They used a large amount of RNA-seq data to identify over 130,000 lincRNAs in Arabidopsis thaliana, Camelina sativa, Brassica rapa, and Eutrema salsugineum. The researchers characterized these lincRNAs using various methods and identified conserved motifs. Additionally, they used comparative genomics and transcriptomics to highlight lincRNAs with sequence or transcriptional conservation and assigned putative functions using guilt-by-association analyses.