A Primate Herpesvirus Uses the Integrator Complex to Generate Viral MicroRNAs

被引:95
作者
Cazalla, Demian [1 ]
Xie, Mingyi [1 ,2 ]
Steitz, Joan A. [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Boyer Ctr Mol Med, Dept Mol Biophys & Biochem, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Boyer Ctr Mol Med, Howard Hughes Med Inst, New Haven, CT 06536 USA
基金
美国国家卫生研究院;
关键词
C-TERMINAL DOMAIN; SMALL NUCLEAR; SMALL RNAS; U1; SNRNA; 3' END; SMN COMPLEX; EXPRESSION; GENES; SEQUENCE; TRANSCRIPTION;
D O I
10.1016/j.molcel.2011.07.025
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
Herpesvirus saimiri (HVS) is a gamma-herpesvirus that expresses Sm class U RNAs (HSURs) in latently infected marmoset T cells. By deep sequencing, we identified six HVS microRNAs (miRNAs) that are derived from three hairpin structures located immediately downstream of the 3' end processing signals of three of the HSURs. The viral miRNAs associate with Ago proteins and are biologically active. We confirmed that the expression of the two classes of viral noncoding RNAs is linked by identifying chimeric HSUR-pre-miRNA transcripts. We show that HVS miRNA biogenesis relies on cis-acting elements specifically required for synthesis and processing of Sm class RNAs. Knockdown of protein components in vivo and processing assays in vitro demonstrated that HVS does not utilize the Microprocessor complex that generates most host miRNAs. Instead, the Integrator complex cleaves to generate the 3' end of the HSUR and the pre-miRNA hairpin. Exportin-5 and Dicer are then required to generate mature viral miRNAs.
引用
收藏
页码:982 / 992
页数:11
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