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EBV Noncoding RNA Binds Nascent RNA to Drive Host PAX5 to Viral DNA
被引:126
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
来源:
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.
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页码:607 / 618
页数:12
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