Your Independent Sequencing Guide
Application Overview > Transcriptome Sequencing
Transcriptome sequencing encompasses a wide variety of applications from simple mRNA profiling to discovery and analysis of the entire transcriptome, including both coding mRNA and non-coding RNA (e.g., miRNA, small RNAs, linc RNAs). These applications, collectively called RNA-Seq, are extremely popular for next generation sequencing platforms as they uncover information that may be missed by array-based platforms, as no prior knowledge of the transcript sequence is needed. RNA-Seq was initially used primarily for discovery applications (rare genes, splice junctions, gene fusions) and with novel or poorly studied organisms for which there weren’t good standard microarrays. However, as the technology is becoming more available and costs are coming down, it is starting to be used for RNA profiling (sample comparison) as well. Also, as it is sequencing based, it is well suited for specialty applications such as RNA editing and allele specific expression. While there are a variety of RNA-Seq applications and protocols, most follow the basic strategy of isolating RNA (such as with poly dT to pull down mRNA), converting it to DNA and then adding adaptor sequences to generate a library suitable for sequencing.
One of the most popular forms of transcriptome sequencing is mRNA-Seq, which targets all polyadenylated mRNA transcripts, or the coding portion of the transcriptome. The depth offered by next generation sequencing is leveraged to find new genes that were undetectable before due to their low level of expression. By the same token, the increased depth and reduced cost of sequencing means these projects can be used to profile gene expression while differentiating between isoforms of the same gene via paired-end reads.
Attempts to target small RNA for sequencing have been driven by interest in microRNAs, as they act as regulatory elements in the transcriptome. By complexing in the 3′ region with mRNA transcripts that have complementary sequence, microRNAs mark these transcripts for degradation prior to translation. The depth offered by next generation sequencing again loans itself to both novel microRNA gene discovery and expression profiling. The major problem in preparing these samples is the difficulty in separating these species from similarly sized adapter-dimers. Gel-based size selections that recover adapter-bound small RNAs while excluding adapter-dimers from the sample are employed here.
The original RNA sequencing method used with next generation sequencing was ‘digital gene expression’ (DGE), a modified form of ‘serial analysis of gene expression’ (SAGE). In this method a single short tag (~23 bases) is generated for each transcript as defined by the relation of a four base restriction enzyme recognition site and the location of the polyA tail. (In practice, additional tags can be generated by the presence of polyA stretches elsewhere in the transcript.) Because each transcript contains only a single tag (or at the most, a few), DGE libraries are substantially less complex than standard RNA-Seq libraries, allowing useful results with fewer reads per sample (1-2M compared with ~30M). Alternatively, higher read depths allow for the detection of extremely rare transcripts, which can be useful when looking for single or low copy transcripts in a population of cells. The SuperSAGE method improves on the original DGE methods through the generation of larger tags, allowing for more precise alignment to the transcriptome. While these methods still have adherents, the rapidly falling costs of sequencing are diminishing the importance of needing fewer reads, while the more comprehensive coverage of the transcriptome by other RNA-Seq methods is gaining in popularity. However, variants of these “tag profiling” methods, such as ‘cap analysis gene expression’ (CAGE), can be very useful for determining the precise 5′ ends of transcripts.
A truly comprehensive view of the transcriptome requires the examination of all unique RNA transcripts for an organism, including both the coding and non-coding portions. This is achieved by combining the results of various RNA-Seq methods. The primary method is the generation of RNA-Seq libraries without the use of polyA enrichment, allowing for the sequencing of a significant portion of the non-coding RNA. However, since rRNA accounts for 95-98% of the transcriptome, it is still necessary to eliminate this fraction prior to sequencing. This is often accomplished with commercially available kits that can use oligos complementary to known rRNA sequences to sequester those transcripts. Alternatively, ‘duplex-specific nuclease’ (or DSN) can be used to eliminate highly abundant sequences, greatly enriching the other portions of the transcriptome. The standard RNA-Seq methods generally don’t capture small RNAs well, so the results are combined with small RNA-Seq and possibly one or more of the CAGE methods to more accurately define the transcription start and stop sites.
Conversion of projects from arrays to sequencing
Increasing sequencing depth
De novo projects
Smaller input amounts
RNA-Seq: Wang, Z. et al. (2009) RNA-Seq: A revolutionary tool for transcriptomics. Nature Reviews Genetics 10(1) (57-63).
miRNA-Seq: Creighton, C. et al. (2009) Expression profiling of microRNAs by deep sequencing. Briefings in Bioinformatics. Vol. 10- No. 5 (490-497).
DGE: Matsumura, H. et al. (2010) High throughput SuperSAGE for digital gene expression analysis of multiple samples using next generation sequencing. PLoS ONE 5(8):e12010.
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