EBV Noncoding RNA Binds Nascent RNA to Drive Host PAX5 to Viral DNA

被引:122
作者
Lee, Nara [1 ]
Moss, Walter N. [1 ]
Yario, Therese A. [1 ]
Steitz, Joan A. [1 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, Dept Mol Biophys & Biochem, New Haven, CT 06536 USA
关键词
EPSTEIN-BARR-VIRUS; B-LYMPHOCYTES; LYTIC CYCLE; RIBOSOMAL-RNA; EBER GENES; CELL-LINE; PROTEIN; TRANSCRIPTION; SEQUENCE; LYMPHOMAGENESIS;
D O I
10.1016/j.cell.2015.01.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
EBER2 is an abundant nuclear noncoding RNA expressed by the Epstein-Barr virus (EBV). Probing its possible chromatin localization by CHART revealed EBER2's presence at the terminal repeats (TRs) of the latent EBV genome, overlapping previously identified binding sites for the B cell transcription factor PAX5. EBER2 interacts with PAX5 and is required for the localization of PAX5 to the TRs. EBER2 knockdown phenocopies PAX5 depletion in upregulating the expression of LMP2A/B and LMP1, genes nearest the TRs. Knockdown of EBER2 also decreases EBV lytic replication, underscoring the essential role of the TRs in viral replication. Recruitment of the EBER2-PAX5 complex is mediated by base-pairing between EBER2 and nascent transcripts from the TR locus. The interaction is evolutionarily conserved in the related primate herpesvirus CeHV15 despite great sequence divergence. Using base-pairing with nascent RNA to guide an interacting transcription factor to its DNA target site is a previously undescribed function for a trans-acting noncoding RNA.
引用
收藏
页码:607 / 618
页数:12
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