TABLE 1.
Techniques | Advantages | Disadvantages | References |
---|---|---|---|
Polysome profiling | RNC-mRNA can be obtained; any length, sequence variation, number of ribosomes on each mRNA can be detected | It is difficult to perform in-depth analysis of all translated mRNA | Chasse et al. (2017) |
RNC-Seq | It can effectively reveal the full-length information of the RNA being translated, including abundance, and type | Prone to ribosome dissociation or RNA degradation after cell lysis; low sequencing precision; no access to ribosome, ORF, uORF information | Wang L et al. (2013) |
TRAP-Seq | RNC-mRNA can be obtained; avoids contamination by eliminating the need for ultracentrifugation; it has the advantage of isolating RNC-mRNA from complex tissues and specific cell types | Stably transfected cell lines need to be established to produce labeled ribosomal proteins; over-labeling of ribosomal proteins may alter the structure and properties of the ribosome | Inada et al. (2002); Heiman et al. (2014) |
Ribo-Seq | Accurately locates genes under translation; accurately quantifies gene translation levels; instantaneously measures translation efficiency; obtains ribosome position, density, ORF, and uORF information | Complex experiment; expensive; can only detect ribosome-protected RNA fragments; poor reproducibility | Ingolia et al. (2009); Ingolia et al. (2019) |