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MicroRNA-141 通过靶向 PPARA 抑制 HBV 复制。

MicroRNA-141 represses HBV replication by targeting PPARA.

机构信息

Beijing Institute of Radiation Medicine, Beijing, People's Republic of China.

出版信息

PLoS One. 2012;7(3):e34165. doi: 10.1371/journal.pone.0034165. Epub 2012 Mar 30.

Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression primarily at the post-transcriptional level and play critical roles in a variety of physiological and pathological processes. In this report, miR-141 was identified to repress HBV expression by screening a small miRNA expressing library and synthetic miR-141 mimics could also significantly suppress HBV expression and replication in HepG2 cells. Bioinformatic analysis and experiment assays indicate that peroxisome proliferator-activated receptor alpha (PPARA) was the target of hsa-miR-141 during this process. Furthermore, knockdown of PPARA by small interfering RNA (siRNA) inhibited HBV replication similar to levels observed for miR-141. Promoter functional analysis indicated that repression of HBV replication by miR-141 mimics or siRNA was mediated by interfering with the HBV promoter functions, consistent with previous studies demonstrating that PPARA regulated HBV gene expression through interactions with HBV promoter regulatory elements. Our results suggest that miR-141 suppressed HBV replication by reducing HBV promoter activities by down-regulating PPARA. This study provides new insights into the molecular mechanisms associated with HBV-host interactions. Furthermore, this information may facilitate the development of novel anti-HBV therapeutic strategies.

摘要

微小 RNA(miRNA)是一种小型非编码 RNA,主要在转录后水平调节基因表达,在多种生理和病理过程中发挥关键作用。本研究通过筛选小型 miRNA 表达文库,鉴定出 miR-141 可抑制 HBV 表达,合成的 miR-141 模拟物也可显著抑制 HepG2 细胞中 HBV 的表达和复制。生物信息学分析和实验验证表明,过氧化物酶体增殖物激活受体α(PPARA)是 hsa-miR-141 在此过程中的靶标。此外,通过小干扰 RNA(siRNA)敲低 PPARA 可抑制 HBV 复制,其抑制效果与 miR-141 相似。启动子功能分析表明,miR-141 模拟物或 siRNA 对 HBV 复制的抑制作用是通过干扰 HBV 启动子功能介导的,这与先前的研究一致,即 PPARA 通过与 HBV 启动子调节元件相互作用来调节 HBV 基因表达。我们的研究结果表明,miR-141 通过下调 PPARA 降低 HBV 启动子活性来抑制 HBV 复制。本研究为 HBV-宿主相互作用的分子机制提供了新的见解。此外,这些信息可能有助于开发新型抗 HBV 治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e313/3316618/bf18f5cdf404/pone.0034165.g001.jpg

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