Format

Send to

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

MicroRNA-141 represses HBV replication by targeting PPARA.

Author information

1
Beijing Institute of Radiation Medicine, Beijing, People's Republic of China.

Erratum in

  • PLoS One. 2012;7(7). doi:10.1371/annotation/cbbe9454-0b72-44b3-a972-10dcaf22db68.

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.

PMID:
22479552
PMCID:
PMC3316618
DOI:
10.1371/journal.pone.0034165
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Public Library of Science Icon for PubMed Central
Loading ...
Support Center