Kaposi's Sarcoma Herpesvirus microRNAs Target Caspase 3 and Regulate Apoptosis

被引:100
作者
Suffert, Guillaume [1 ]
Malterer, Georg [2 ]
Hausser, Jean [3 ,4 ]
Viiliainen, Johanna [5 ,6 ]
Fender, Aurelie [1 ]
Contrant, Maud [1 ]
Ivacevic, Tomi [7 ]
Benes, Vladimir [7 ]
Gros, Frederic [8 ]
Voinnet, Olivier [9 ]
Zavolan, Mihaela [3 ,4 ]
Ojala, Paivi M. [5 ,6 ,10 ]
Haas, Juergen G. [2 ,11 ]
Pfeffer, Sebastien [1 ]
机构
[1] Univ Strasbourg, Inst Biol Mol & Cellulaire, CNRS, Architecture & React ARN, Strasbourg, France
[2] Univ Munich, Max Von Pettenkofer Inst, Munich, Germany
[3] Univ Basel, Biozentrum, Basel, Switzerland
[4] Swiss Inst Bioinformat, Basel, Switzerland
[5] Univ Helsinki, Biomedicum Helsinki, Genome Scale Biol Program, Helsinki, Finland
[6] Univ Helsinki, Inst Biomed, Helsinki, Finland
[7] EMBL, GeneCore Genom Core Facil, Heidelberg, Germany
[8] Univ Strasbourg, Inst Biol Mol & Cellulaire, CNRS, Immunol & Chim Therapeut UPR 9021, Strasbourg, France
[9] CNRS, Inst Biol Mol Plantes, F-67084 Strasbourg, France
[10] Fdn Finnish Canc Inst, Helsinki, Finland
[11] Univ Edinburgh, Sch Med, Div Pathway Med, Edinburgh, Midlothian, Scotland
基金
欧洲研究理事会; 芬兰科学院;
关键词
CELL-LINE; EXPRESSION; PROTEIN; IDENTIFICATION; BIOGENESIS; DEATH; ESTABLISHMENT; REPLICATION; RECEPTORS; INFECTION;
D O I
10.1371/journal.ppat.1002405
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Kaposi's sarcoma herpesvirus (KSHV) encodes a cluster of twelve micro (mi)RNAs, which are abundantly expressed during both latent and lytic infection. Previous studies reported that KSHV is able to inhibit apoptosis during latent infection; we thus tested the involvement of viral miRNAs in this process. We found that both HEK293 epithelial cells and DG75 cells stably expressing KSHV miRNAs were protected from apoptosis. Potential cellular targets that were significantly down-regulated upon KSHV miRNAs expression were identified by microarray profiling. Among them, we validated by luciferase reporter assays, quantitative PCR and western blotting caspase 3 (Casp3), a critical factor for the control of apoptosis. Using site-directed mutagenesis, we found that three KSHV miRNAs, miR-K12-1, 3 and 4-3p, were responsible for the targeting of Casp3. Specific inhibition of these miRNAs in KSHV-infected cells resulted in increased expression levels of endogenous Casp3 and enhanced apoptosis. Altogether, our results suggest that KSHV miRNAs directly participate in the previously reported inhibition of apoptosis by the virus, and are thus likely to play a role in KSHV-induced oncogenesis.
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页数:18
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