
The EMBO Journal, Год журнала: 2025, Номер unknown
Опубликована: Май 27, 2025
Abstract The three-dimensional (3D) chromatin structure of Epstein–Barr virus (EBV) within host cells and the underlying mechanisms interaction gene regulation, particularly those involving EBV’s noncoding RNAs (ncRNAs), have remained incompletely characterized. In this study, we employed state-of-the-art techniques 3D genome mapping, including protein-associated analysis with paired-end tag sequencing (ChIA-PET), RNA-associated technique (RDD), super-resolution microscopy, to delineate spatial architecture EBV in human lymphoblastoid cells. We systematically analyzed EBV-to-EBV (E–E), EBV-to-host (E–H), host-to-host (H–H) interactions linked proteins RNAs. Our findings reveal that utilizes CCCTC-binding factor (CTCF) RNA polymerase II (RNAPII) form distinct contact domains (CCDs) RNAPII-associated (RAIDs). anchors these serve as platforms for extensive chromatin, thus modulating expression. Notably, ncRNAs, especially Epstein–Barr-encoded (EBERs), target interact less accessible regions repress a subset genes via inhibition loops. This process involves cofactor nucleolin (NCL) its recognition motifs, depletion either NCL or EBERs alters expression crucial infection control, immune response, cell cycle regulation. These unveil sophisticated interplay between chromatin.
Язык: Английский