Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencing

The majority of the human genome is differentially expressed across a wide dynamic range to produce a spectrum of protein-coding and noncoding RNAs, generating a transcriptome of unexpected scale and complexity. These features present a challenge for gene-expression profiling with qRT-PCR and RNA-seq. qRT-PCR is ill suited for discovering genes, resolving alternative splicing or characterizing whole transcriptomes. RNA-seq measures global gene abundance and splicing but provides scant coverage of rare transcripts, which limits the sensitivity of transcript assembly and quantification. Researchers from the Garvan Institute of Medical Research recently developed CaptureSeq, which enriches transcripts of interest by hybridizing them to magnetic bead-linked oligonucleotides that are tiled across the region of interest, allowing for targeted purification, multiplexed library preparation and RNA sequencing at a high depth.

To assess CaptureSeq’s quantitative accuracy, the researchers undertook an analysis of transcript quantification in direct comparison to conventional RNA-seq and qRT-PCR. As an independent reference, External RNA Control Consortium (ERCC) RNA standards spanning an ~106-fold range of concentrations were spiked into three biological-replicate human K562 RNA samples. They then performed CaptureSeq on each sample, targeting the full range of standards, along with matched RNA-seq.

CaptureSeq exhibited high correlation between biological and technical replicates (mean Spearman’s r ≥ 0.998 in measured ERCC standard abundance; similar to matched RNA-seq (Spearman’s r = 0.991). CaptureSeq was superior for the detection and quantification of genes with low expression, showed little technical variation and accurately measured differential expression. By clustering lncRNA expression levels across human tissues, the researchers also identified coexpressed subsets of lncRNAs, which provided a greatly expanded atlas of lncRNA expression.

Tissue-specific expression of captured lncRNAs


(a) Hierarchal clustering of lncRNA loci according to expression. (b) Example of brain-specific lncRNA Evf2 correctly assembled and quantified using CaptureSeq.

Clark MB, Mercer TR, Bussotti G, Leonardi T, Haynes KR, Crawford J, Brunck ME, Cao KA, Thomas GP, Chen WY, Taft RJ, Nielsen LK, Enright AJ, Mattick JS, Dinger ME. (2015) Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencing. Nat Methods 12(4):339-42. [abstract]

Leave a Reply

Your email address will not be published. Required fields are marked *