Viral MicroRNA Targetome of KSHV-Infected Primary Effusion Lymphoma Cell Lines

被引:257
|
作者
Gottwein, Eva [1 ]
Corcoran, David L. [2 ]
Mukherjee, Neelanjan [2 ]
Skalsky, Rebecca L. [4 ]
Hafner, Markus [5 ,6 ]
Nusbaum, Jeffrey D. [5 ,6 ]
Shamulailatpam, Priscilla [1 ]
Love, Cassandra L. [2 ]
Dave, Sandeep S. [2 ]
Tuschl, Thomas [5 ,6 ]
Ohler, Uwe [2 ,3 ]
Cullen, Bryan R. [4 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Microbiol Immunol, Chicago, IL 60611 USA
[2] Duke Univ, Duke Inst Genome Sci & Policy, Durham, NC 27708 USA
[3] Duke Univ, Dept Biostat & Bioinformat, Durham, NC 27708 USA
[4] Duke Univ, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[5] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10065 USA
[6] Rockefeller Univ, Lab RNA Mol Biol, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
SARCOMA-ASSOCIATED HERPESVIRUS; VIRUS-ENCODED MICRORNAS; HUMAN GAMMA-HERPESVIRUSES; EPSTEIN-BARR-VIRUS; PROTEIN EXPRESSION; MESSENGER-RNAS; DNA-SEQUENCES; PAR-CLIP; IDENTIFICATION; MIR-155;
D O I
10.1016/j.chom.2011.09.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Primary effusion lymphoma (PEL) is caused by Kaposi's sarcoma-associated herpesvirus (KSHV) and frequently also harbors Epstein-Barr virus (EBV). The expression of KSHV- and EBV-encoded microRNAs (miRNAs) in PELs suggests a role for these miRNAs in latency and lymphomagenesis. Using PAR-CLIP, a technology which allows the direct and transcriptome-wide identification of miRNA targets, we delineate the target sites for all viral and cellular miRNAs expressed in PEL cell lines. The resulting data set revealed that KSHV miRNAs directly target more than 2000 cellular mRNAs, including many involved in pathways relevant to KSHV pathogenesis. Moreover, 58% of these mRNAs are also targeted by EBV miRNAs, via distinct binding sites. In addition to a known viral analog of cellular miR-155, we show that KSHV encodes a viral miRNA that mimics cellular miR-142-3p function. In summary, this study identifies an extensive list of KSHV miRNA targets, which are likely to influence viral replication and pathogenesis.
引用
收藏
页码:515 / 526
页数:12
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