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Published on: May 1, 2021
Identification of miRNAs encoded by Autographa californica nucleopolyhedrovirus
Jinwen Wang1, Ke Xing2, Peiwen Xiong1
1School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, PR China.
Abstract:
Two Autographa californica nucleopolyhedrovirus (AcMNPV) encoded miRNAs, AcMNPV-miR-1 and AcMNPV-miR-3, have been reported by us in 2013 and 2019, respectively. Here, we present an integrated investigation of AcMNPV-encoded miRNAs, which include the above two miRNAs and three additional newly identified miRNAs. Six candidate miRNAs were predicted through small RNA deep sequencing and bioinformatics, of which, five were validated. Three miRNAs are located opposite the coding sequences, the other two are located in the coding sequences of viral genes. Targets in both virus and host were predicted and subsequently tested using dual-luciferase reporter assays. The validated targets were found mainly in AcMNPV, except for the targets of AcMNPV-miR-4, which are all host genes. Based on reporter assays, the five miRNAs predominantly function by down-regulating their targets. The transcription start sites of these miRNAs were bioinformatic screened based on known baculovirus promoter motifs. Our study reveals that AcMNPV-encoded miRNAs function as fine modulators of the interactions between host and virus by regulating viral and/or host genes.
Insights
This study identifies five Autographa californica nucleopolyhedrovirus (AcMNPV)-encoded microRNAs (miRNAs) that regulate viral and host genes. These AcMNPV miRNAs fine-tune virus-host interactions by down-regulating gene expression.
Area of Science:
- Virology
- Molecular Biology
- Genomics
Background:
- Autographa californica nucleopolyhedrovirus (AcMNPV) encodes microRNAs (miRNAs) that influence virus-host interactions.
- Previous studies identified AcMNPV-miR-1 and AcMNPV-miR-3.
Purpose of the Study:
- To comprehensively investigate AcMNPV-encoded miRNAs, including newly identified ones.
- To characterize the targets and regulatory functions of these viral miRNAs.
Main Methods:
- Small RNA deep sequencing and bioinformatics for miRNA prediction.
- Dual-luciferase reporter assays to validate miRNA targets and functions.
- Bioinformatic screening of transcription start sites using baculovirus promoter motifs.
Main Results:
- Five AcMNPV-encoded miRNAs were validated, with three located intergenically and two within viral gene coding sequences.
- Validated targets were primarily viral, except for AcMNPV-miR-4 targeting host genes.
- Reporter assays confirmed that these miRNAs predominantly down-regulate their targets.
Conclusions:
- AcMNPV-encoded miRNAs act as fine modulators in virus-host interactions.
- These miRNAs regulate both viral and host genes, impacting the infection process.
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