Key result
UV-C light exposure induced selective RNA self-cleavage within the highly structured 5'-genomic regions of Hepatitis C Virus and Classic Swine Fever Virus.
The discovery of UV-C-activated ribozyme activity in viral RNAs suggests that photosensitive RNA structures may have mediated early RNA self-cleavage events.
UV-C-induced viral RNA cleavage is hypothesis-generating; leaves open photosensitive ribozymes as potential antiviral or evolutionary targets.
A novel UV-C-light-induced ribozyme activity was discovered within the highly structured 5'-genomic regions of both Hepatitis C Virus (HCV) and the related Classic Swine Fever Virus (CSFV). Cleavage is mediated by exposure to UV-C light but not by exogenous oxygen radicals. It is also very selective, occurring at base positions HCV C(79) and CSFV A(45) in some molecules and at the immediately adjacent 5'-positions HCV U(78) and CSFV U(44) in others. Among other reaction products, the majority of biochemically active products detected contained 3'-phosphate and 5'-phosphate-end groups at the newly generated termini, along with a much lower amount of 3'-hydroxyl end group. While preservation of an E-loop RNA structure in the vicinity of the cleavage site was a requisite for HCV RNA self-cleavage, this was not the case for CSFV RNA. The short size of the reactive domains (~33 nt), which are compatible with primitive RNA motifs, and the lack of sequence homology, indicate that as-yet unidentified UV-activated ribozymes are likely to be found throughout structured RNAs, thereby providing clues to whether early RNA self-cleavage events were mediated by photosensitive RNA structures.
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Ariza‐Mateos et al. (2011) studied this question. UV-C light exposure vs. Exogenous oxygen radicals was evaluated on RNA self-cleavage. UV-C light exposure induced selective RNA self-cleavage within the highly structured 5'-genomic regions of Hepatitis C Virus and Classic Swine Fever Virus.
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