Divergent MicroRNA Targetomes of Closely Related Circulating Strains of a Polyomavirus

被引:20
作者
Chen, Chun Jung [1 ]
Cox, Jennifer E. [1 ]
Kincaid, Rodney P. [1 ]
Martinez, Angel [2 ]
Sullivan, Christopher S. [1 ]
机构
[1] Univ Texas Austin, Austin, TX 78712 USA
[2] James Bowie High Sch, Amer Chem Soc Project SEED Summer Internship Prog, Austin, TX USA
基金
美国国家卫生研究院;
关键词
HUMAN GAMMA-HERPESVIRUSES; EPSTEIN-BARR-VIRUS; SHORT HAIRPIN RNAS; LARGE GENE LISTS; NUCLEAR EXPORT; VIRAL MICRORNA; MESSENGER-RNA; INTERFERING RNAS; BINDING PROTEIN; EXPRESSION;
D O I
10.1128/JVI.01711-13
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Hundreds of virus-encoded microRNAs (miRNAs) have been uncovered, but an in-depth functional understanding is lacking for most. A major challenge for the field is separating those miRNA targets that are biologically relevant from those that are not advantageous to the virus. Here, we show that miRNAs from related variants of the polyomavirus simian vacuolating virus 40 (SV40) have differing host target repertoires (targetomes) while their direct autoregulatory activity on virus-encoded early gene products is completely preserved. These results underscore the importance of miRNA-mediated viral gene autoregulation in some polyomavirus life cycles. More broadly, these findings imply that some host targets of virus-encoded miRNAs are likely to be of little selective advantage to the virus, and our approach provides a strategy for prioritizing relevant targets.
引用
收藏
页码:11135 / 11147
页数:13
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