Chemical ligation |
• Only chemical reagents |
• Low ligating efficiency |
• No biological components |
• Biosafety concern |
• 2′, 5′-phosphodiester bonds |
Enzymatic ligation |
T4 DNA ligase |
• Accurate |
• Affected by significant RNA secondary structure |
• Affected by high percentage of Us |
• Low efficiency |
• Intermolecular end joining side reactions |
T4 RNA ligase 1 |
• High efficiency |
• Low ligating efficiency for large RNA molecules |
• Synthesize as little as 6 to 8 nucleotides of circRNAs |
• Affected by significant RNA secondary structure |
• Intermolecular end joining side reactions |
T4 RNA ligase 2 |
• More efficient for linear RNA precursor folding into a secondary structure with the ligation junction in a double-stranded region |
• Low ligating efficiency for large RNA molecules |
• Intermolecular end joining side reactions |
Ribozyme method |
Group I intron self-splicing system |
• Simple reaction condition and purification method |
• Affected by significant RNA secondary structure |
• Can be used for RNA cyclization in vitro and in vivo
|
• Can synthesize large circRNAs |
Group II intron self-splicing system |
• Accurate ligation |
• 2′, 5′-phosphodiester bonds |
• The mechanism remains unclear in vitro
|
Hairpin ribozyme method |
• High efficiency for small circRNAs |
• Unstable |
• Exogenous HPR sequences |