Table 1.
Characteristics | miRNA | lncRNAs |
---|---|---|
Size | Short (18 to 21 nucleotides) | >200 nucleotides |
Primary mode of action | Negatively regulating the expression by complementary binding to target mRNAs and causing their degradation or inhibiting translation | Highly diverse, regulate gene expression by
various mechanisms. Lnc-RNAs may work as 1. Signaling cues 2. Guides 3. Decoys 4. Scaffolds 5. miRNA sponges |
Genomic location |
-Exonic -Intergenic (between genes) -Intronic (embedded in a gene) |
-Antisense
RNA -LincRNA -Sense overlapping RNA -Sense intronic RNA - 3’ overlapping ncRNA |
Secondary structure | Usually the precursor miRNA forms a hairpin structure | Forms simple to complex secondary structures 59, 60 |
Post-transcriptional processing | Typically produced as pri-miRNAs, which are processed by miRNA-processing enzymes (Drosha, DGCR8) and Dicer to generate pre-miR and mature miRNAs | Undergo post-transcriptional processing like mRNAs, i.e. 5’ capping, polyadenylation, and splicing |
Computational gene target prediction | Relatively easy. Multiple bioinformatics tools/ prediction algorithms available that help to predict target genes | Difficult to predict. Not available. |
Conservation between species | Relatively well conserved nucleotide sequences across species, although some species-specific miRNAs exist | Poorly conserved between species at the level of primary nucleotide sequences, but may have conserved secondary structures |
Experimental gain-of-function strategies | miRNA mimics, over-expression plasmids, transgenic overexpression | over-expression plasmids, transgenic overexpression |
Experimental loss-of-function strategies | Anti-miRs, antagomiRs, and morpholinos, genetic deletions | GapmeRs, genetic deletions or mutations |