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Biology subjects

Meher, A.

Publications and source records attributed to Meher, A..

2 recordsLinked to original sources

A novel role of circCPSF6 regulating antiviral innate immunity via miR-665 and PCBP2-IPS-1 axis

ObjectiveCircular RNAs are emerging as critical regulators of biological processes, yet their contribution to innate immune response during virus infection remains insufficiently defined. This study investigated the role of circCPSF6 in modulating host antiviral responses. MethodCircCPSF6 expression was validated in human and murine cells and tissue by RT-PCR and digital PCR. Its effect on virus replication was analysed by RT-PCR in human and murine primary cells and cytokine production at protein level was measured by ELISA. Luciferase assay, RNA immunoprecipitation, RNA pulldown assay, immunoblotting was performed to explore the circRNA-miRNA regulatory mechanism. CircCPSF6 interacting protein were identified by RNA pulldown followed by mass spectrometry and regulatory mechanism was analysed by immunoblotting and confocal microscopy. ResultCircCPSF6 identified as highly conserved circRNA, suppressed during virus infection, in vitro and in vivo. Functional analyses revealed antiviral role of circCPSF6. Mechanistically, circCPSF6 has dual cross-regulatory role by sequestering proviral miR-665 to relieve expression of key antiviral genes (MyD88, STAT2, IKK{varepsilon}) and interact with RNA binding protein PCBP2 to modulate IPS-1 degradation. ConclusionCircCPSF6 exert antiviral role and regulate host innate immune signaling by direct RNA-RNA and RNA-protein interaction, highlights circRNA mediated network as a potential therapeutic target in virus infection. HighlightsCircCPSF6 is evolutionarily conserved and suppressed during virus infection. CircCPSF6 act as antiviral factor by promoting inflammatory cytokine production. CircCPSF6 sponges proviral miR-665 and alleviate MyD88, STAT2, IKK{varepsilon} expression. CircCPSF6 bind to PCBP2, limit IPS-1 degradation and sustain antiviral signaling. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=151 SRC="FIGDIR/small/686289v1_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@f59bedorg.highwire.dtl.DTLVardef@cff26eorg.highwire.dtl.DTLVardef@354ea5org.highwire.dtl.DTLVardef@1be4c63_HPS_FORMAT_FIGEXP M_FIG Mechanism of host innate immune regulation by circCPSF6 during virus infection. In cell cytoplasm circCPSF6 act as ceRNA for miR-665 and RNA binding protein PCBP2. Virus infection leads to reduced circCPSF6 and increased miR-665 expression, which inhibits expression of antiviral genes, MyD88, STAT2, IKK{varepsilon}. Additionally, reduced circCPSF6 leads to elevated free PCBP2 protein, hence, promote PCBP2 mediated IPS-1 degradation. Overall, these effects contribute to reduced innate immune response and increased viral replication. C_FIG

immunology↗

Immunometabolic role of metabolic enzyme PANK4 in regulation of TLR7/9-mediated innate immunity

Innate immune responses are intimately linked to cellular metabolism, yet the molecular connections between metabolic reprogramming and antiviral defense remain incompletely defined. Here, we identify PANK4, an atypical member of pantothenate kinase family involved in coenzyme A (CoA) biosynthesis, as an unexpected regulator of RNA virus including influenza virus pathogenesis. Unlike other pantothenate kinases, PANK4 lacks canonical kinase activity but has been implicated in metabolic regulation. We show that influenza virus infection, in conjunction with pantothenic acid, induces PANK4 expression, which promotes viral replication by enhancing glucose uptake and glycolytic activity. Loss of PANK4 curtailed viral replication, reduced expression of glycolytic regulators, and heightened host antiviral defenses. Mechanistically, PANK4 interacts with UNC93B1 to suppress TLR7 and TLR9 mediated cytokine responses, thereby acting as a negative regulator of nucleic acid-sensing innate immune pathways in various cell-types. Furthermore, viral proteins NS1 and PB1 exploit PANK4 to amplify replication and immune evasion.

immunology↗