Abstract
In this study, we employed short- and long-read sequencing technologies to delineate the transcriptional architecture of the human monkeypox virus and to identify key regulatory elements that govern its gene expression. Specifically, we conducted a transcriptomic analysis to annotate the transcription start sites (TSSs) and transcription end sites (TESs) of the virus by utilizing cap analysis of gene expression sequencing on the Illumina platform and direct RNA sequencing on the Oxford Nanopore technology device. Our investigations uncovered significant complexity in the use of alternative TSSs and TESs in viral genes. In this research, we also detected the promoter elements and poly(A) signals associated with the viral genes. Additionally, we identified novel genes in both the left and right variable regions of the viral genome.
Importance Generally, gaining insight into how the transcription of a virus is regulated offers insights into the key mechanisms that control its life cycle. The recent outbreak of the human monkeypox virus has underscored the necessity of understanding the basic biology of its causative agent. Our results are pivotal for constructing a comprehensive transcriptomic atlas of the human monkeypox virus, providing valuable resources for future studies.
Abbreviations
- CAGE
- cap analysis of gene expression
- cDNA-Seq
- cDNA sequencing
- dRNA-Seq
- direct RNA sequencing
- ePAS
- early poly(A)-signal
- LRS
- long-read sequencing
- hMPXV
- human monkeypox virus
- PAS
- poly(A)-signal
- PR
- post-replicative
- SRS
- short-read sequencing
- TES
- transcription end site
- TSS
- transcription start site
- VACV
- Vaccinia virus