The roles of nuclear orphan receptor NR2F6 in anti-viral innate immunity.

PLoS Pathog

Frontier Science Center for Immunology and Metabolism, Hubei Key Laboratory of Cell Homeostasis, Hubei Key Laboratory of Developmentally Originated Disease, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, China.

Published: June 2024

AI Article Synopsis

  • Proper regulation of transcription factors like IRF3 is essential for the body's defense against viruses.
  • Through epigenomic analysis, researchers identified three new transcription factors (NR2F6, MEF2D, MAFF) that enhance HSV-1 replication.
  • NR2F6 promotes HSV-1 replication independently of the cGAS/STING pathway but is also repressed by c-Jun and affected by signaling from the cGAS/STING innate immunity pathway.

Article Abstract

Proper transcription regulation by key transcription factors, such as IRF3, is critical for anti-viral defense. Dynamics of enhancer activity play important roles in many biological processes, and epigenomic analysis is used to determine the involved enhancers and transcription factors. To determine new transcription factors in anti-DNA-virus response, we have performed H3K27ac ChIP-Seq and identified three transcription factors, NR2F6, MEF2D and MAFF, in promoting HSV-1 replication. NR2F6 promotes HSV-1 replication and gene expression in vitro and in vivo, but not dependent on cGAS/STING pathway. NR2F6 binds to the promoter of MAP3K5 and activates AP-1/c-Jun pathway, which is critical for DNA virus replication. On the other hand, NR2F6 is transcriptionally repressed by c-Jun and forms a negative feedback loop. Meanwhile, cGAS/STING innate immunity signaling represses NR2F6 through STAT3. Taken together, we have identified new transcription factors and revealed the underlying mechanisms involved in the network between DNA viruses and host cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11175508PMC
http://dx.doi.org/10.1371/journal.ppat.1012271DOI Listing

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