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MicroRNA-141 Represses HBV Replication by Targeting PPARA

机译:MicroRNA-141通过靶向PPARA抑制HBV复制

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摘要

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.
机译:微小RNA(miRNA)是小的非编码RNA,主要在转录后水平调节基因表达,并在各种生理和病理过程中发挥关键作用。在本报告中,通过筛选小的miRNA表达文库鉴定了miR-141可以抑制HBV表达,合成的miR-141模仿物也可以显着抑制HBV在HepG2细胞中的表达和复制。生物信息学分析和实验分析表明,过氧化物酶体增殖物激活受体α(PPARA)是此过程中hsa-miR-141的目标。此外,通过小干扰RNA(siRNA)抑制PPARA可抑制HBV复制,类似于miR-141观察到的水平。启动子功能分析表明,miR-141模仿物或siRNA抑制HBV复制是通过干扰HBV启动子功能来介导的,这与以前的研究表明PPARA通过与HBV启动子调控元件的相互作用调节了HBV基因表达有关。我们的结果表明,miR-141通过下调PPARA降低HBV启动子活性来抑制HBV复制。这项研究提供了与HBV-宿主相互作用相关的分子机制的新见解。此外,该信息可以促进新的抗HBV治疗策略的发展。

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