 |
 |
GEO help: Mouse over screen elements for information. |
|
| Status |
Public on May 20, 2024 |
| Title |
Epitranscriptomic cytidine methylation of the Hepatitis B viral RNA encapsidation signal ensure the reverse transcription of viral RNA [PAR-CLIP] |
| Organism |
Homo sapiens |
| Experiment type |
Other
|
| Summary |
Epitranscriptomic RNA modifications have emerged as important regulators of the fate and function of both cellular and viral RNAs. One prominent modification, the cytidine methylation 5-methylcytidine (m5C), is found on the RNA of HIV-1, where m5C enhances the translation and splicing of HIV-1 RNA. However, whether m5C functionally enhances the RNA of other pathogenic viruses remain elusive. Here, we report that the RNA of hepatitis B virus (HBV) is enriched with a high level of m5C, mediated mainly through the cellular methyltransferase NSUN2. Intrigingly, the most prominent cluster of NSUN2-deposited m5C is found on the epsilon hairpin, an RNA element required for viral RNA encapsidation and reverse transcription. Loss of m5C from HBV RNA due to depletion of NSUN2 resulted in a modest decrease in viral capsid protein (HBc) translation, yet this is accompaneied by a near-complete loss of the reverse transcribed viral DNA. Similarly, mutations introduced to remove the methylated cytidines resulted in a translation decrease and block of reverse transcription. Furthermore, pharmacological disruption of m5C deposition with a nucleoside analogue led to a significant decrease in HBV replication. Thus, our data indicates m5C methylations is a critical enhancer of the epsilon element in HBV reverse transcription. Our study suggests the theraputic potential of targeting the m5C methyltransfer process on the HBV 5’epsilon as an alternative antiviral stratagy.
|
| |
|
| Overall design |
PAR-CLIP: HuH-7 cells, transfected with HBV replicon plasmid along with FLAG-GFP or FLAG-NSUN2 expression plasmids, were lysed and subject to FLAG-antibody pulldown of proteins, the co-immunoprecipitated RNA isolated and sequenced.
|
| |
|
| Contributor(s) |
Su P, Tsai K |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| Submission date |
Dec 13, 2023 |
| Last update date |
May 20, 2024 |
| Contact name |
Kevin Tsai |
| E-mail(s) |
kevtsai@ibms.sinica.edu.tw
|
| Organization name |
Academia Sinica
|
| Department |
Institute of Biomedical Sciences
|
| Lab |
R414
|
| Street address |
128 Sec. 2, Academia Rd. Nankang
|
| City |
Taipei |
| ZIP/Postal code |
115 |
| Country |
Taiwan |
| |
|
| Platforms (1) |
| GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
|
| Samples (2) |
| GSM7974008 |
GFP transfected HuH-7, HBV transfected, PAR-CLIP |
| GSM7974009 |
NSUN2-transfected HuH-7, HBV transfected, PAR-CLIP |
|
| This SubSeries is part of SuperSeries: |
| GSE250109 |
Epitranscriptomic cytidine methylation of the Hepatitis B viral RNA encapsidation signal ensure the reverse transcription of viral RNA |
|
| Relations |
| BioProject |
PRJNA1052037 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE250108_RAW.tar |
10.0 Kb |
(http)(custom) |
TAR (of BED) |
SRA Run Selector |
| Raw data are available in SRA |
|
|
|
|
 |
