GCRV-encoded circRNA circ_20 forms a ternary complex with BIP and PERK to delay virus replication by inhibiting the PERK-eIF2α pathway
- Int J Biol Macromol. 2024 Nov;281(Pt 2):136314. doi: 10.1016/j.ijbiomac.2024.136314.
- 1. School of Life Sciences, Soochow University, Suzhou 21523, China.
- 2. School of Chemistry and Life Science, Suzhou University of Science and Technology, Suzhou 215009, China.
- 3. School of Life Sciences, Soochow University, Suzhou 21523, China. Electronic address: [email protected].
- 4. School of Life Sciences, Soochow University, Suzhou 21523, China. Electronic address: [email protected].
Viral circRNAs play important roles in host-virus interactions. Previous reports showed that grass carp reovirus (GCRV) encodes 32 circRNAs, and circ_20 from the negative strand of GCRV genome segment 7 has the potential to regulate GCRV replication. However, the regulatory mechanism of circ_20 on GCRV remains unknown. In this study, circ_20 was further validated, and circ_20 negatively regulated ERS, the PERK pathway, and ROS production in GCRV-infected cells. Furthermore, circ_20 inhibited the PERK pathway by forming a ternary complex with BIP and PERK, resulting in delaying GCRV replication. RNA pull-down results indicated that the 51-102 nt region of circ_20 interacts with BIP, while the 451-502 and 514-565 nt regions interact with PERK. After the deletion of these interaction regions, the ability of circ_20 to promote BIP-PERK interaction decreases, leading to a decrease in the ability to inhibit GCRV proliferation. These findings uncovered new insights into the complex interplay between viruses and host cells and provided a novel understanding of the significance of viral circRNAs in virus-host interactions.
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