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草鱼呼肠孤病毒体外抑制 RNA 干扰途径。

Suppression of RNA interference pathway in vitro by Grass carp reovirus.

机构信息

Key Laboratory of Aquatic Genetic Resources and Utilization /Ministry of Agriculture, Shanghai Ocean University, Shanghai 201306, China.

出版信息

Virol Sin. 2012 Apr;27(2):109-19. doi: 10.1007/s12250-012-3230-4. Epub 2012 Apr 11.

Abstract

The means of survival of genomic dsRNA of reoviruses from dsRNA-triggered and Dicer-initiated RNAi pathway remains to be defined. The present study aimed to investigate the effect of Grass carp reovirus (GCRV) replication on the RNAi pathway of grass carp kidney cells (CIK). The dsRNA-triggered RNAi pathway was demonstrated unimpaired in CIK cells through RNAi assay. GCRV-specific siRNA was generated in CIK cells transfected with purified GCRV genomic dsRNA in Northern blot analysis; while in GCRV-infected CIK cells, no GCRV-specific siRNA could be detected. Infection and transfection experiments further indicated that replication of GCRV correlated with the increased transcription level of the Dicer gene and functional inhibition of in vitro synthesized egfp-siRNA in silencing the EGFP reporter gene. These data demonstrated that although only the genomic dsRNA of GCRV was sensitive to the cellular RNAi pathway, unidentified RNAi suppressor protein(s) might contribute to the survival of the viral genome and efficient viral replication.

摘要

呼肠孤病毒基因组 dsRNA 利用 dsRNA 触发和 Dicer 起始的 RNAi 通路进行生存的方式仍有待确定。本研究旨在探究草鱼呼肠孤病毒(GCRV)复制对草鱼肾脏细胞(CIK)的 RNAi 通路的影响。通过 RNAi 实验,证明 CIK 细胞中的 dsRNA 触发的 RNAi 通路未受影响。在 Northern blot 分析中,用纯化的 GCRV 基因组 dsRNA 转染 CIK 细胞后产生了 GCRV 特异性 siRNA;而在 GCRV 感染的 CIK 细胞中,无法检测到 GCRV 特异性 siRNA。感染和转染实验进一步表明,GCRV 的复制与 Dicer 基因转录水平的增加以及体外合成的 egfp-siRNA 对 EGFP 报告基因的抑制功能相关。这些数据表明,尽管只有 GCRV 的基因组 dsRNA 对细胞 RNAi 通路敏感,但未鉴定的 RNAi 抑制蛋白(s)可能有助于病毒基因组的存活和病毒的有效复制。

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