Exploring RNA modifications in infectious non-coding circular RNAs
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
39883038
PubMed Central
PMC11817525
DOI
10.1080/15476286.2025.2459039
Knihovny.cz E-zdroje
- Klíčová slova
- 6-methyladenosine, LC-MS, m6A SELECT, RNA modification, Viroid, direct RNA-seq,
- MeSH
- konformace nukleové kyseliny MeSH
- kruhová RNA * genetika metabolismus MeSH
- nemoci rostlin virologie MeSH
- posttranskripční úpravy RNA * MeSH
- replikace viru MeSH
- RNA virová * genetika metabolismus chemie MeSH
- sekvenční analýza RNA MeSH
- viroidy * genetika MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- kruhová RNA * MeSH
- RNA virová * MeSH
Viroids, small circular non-coding RNAs, act as infectious pathogens in higher plants, demonstrating high stability despite consisting solely of naked RNA. Their dependence of replication on host machinery poses the question of whether RNA modifications play a role in viroid biology. Here, we explore RNA modifications in the avocado sunblotch viroid (ASBVd) and the citrus exocortis viroid (CEVd), representative members of viroids replicating in chloroplasts and the nucleus, respectively, using LC - MS and Oxford Nanopore Technology (ONT) direct RNA sequencing. Although no modification was detected in ASBVd, CEVd contained approximately one m6A per RNA molecule. ONT sequencing predicted three m6A positions. Employing orthogonal SELECT method, we confirmed m6A in two positions A353 and A360, which are highly conserved among CEVd variants. These positions are located in the left terminal region of the CEVd rod-like structure where likely RNA Pol II and and TFIIIA-7ZF bind, thus suggesting potential biological role of methylation in viroid replication.
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Boccaletto P, Machnicka MA, Purta E, et al. MODOMICS: a database of RNA modification pathways. 2017 update. Nucleic Acids Res. 2017;46(D1):D303–D307. doi: 10.1093/nar/gkx1030 PubMed DOI PMC
Sloan KE, Warda AS, Sharma S, et al. Tuning the ribosome: the influence of rRNA modification on eukaryotic ribosome biogenesis and function. RNA Biol. 2017;14(9):1138–1152. doi: 10.1080/15476286.2016.1259781 PubMed DOI PMC
Wilkinson E, Cui Y-H, He Y-Y.. Roles of RNA modifications in diverse cellular functions. Front Cell Dev Biol. 2022;10:10. doi: 10.3389/fcell.2022.828683 PubMed DOI PMC
Zhang W, Foo M, Eren AM, et al. tRNA modification dynamics from individual organisms to metaepitranscriptomics of microbiomes. Mol Cell. 2022;82(5):891–906. doi: 10.1016/j.molcel.2021.12.007 PubMed DOI PMC
Shi H, Chai P, Jia R, et al. Novel insight into the regulatory roles of diverse RNA modifications: re-defining the bridge between transcription and translation. Mol Cancer. 2020;19(1):78. doi: 10.1186/s12943-020-01194-6 PubMed DOI PMC
Patrasso EA, Raikundalia S, Arango D. Regulation of the epigenome through RNA modifications. Chromosoma. 2023;132(3):231–246. doi: 10.1007/s00412-023-00794-7 PubMed DOI PMC
Wiener D, Schwartz S. The epitranscriptome beyond m6A. Nat Rev Genet. 2021;22(2):119–131. doi: 10.1038/s41576-020-00295-8 PubMed DOI
Ammann G, Berg M, Dalwigk JF, et al. Pitfalls in RNA modification quantification using nucleoside mass spectrometry. Acc Chem Res. 2023;56(22):3121–3131. doi: 10.1021/acs.accounts.3c00402 PubMed DOI PMC
Potužník JF, Cahová H, Prasad VR, et al. It’s the little things (in viral RNA). mBio. 2020;11(5):e02131–20. doi: 10.1128/mBio.02131-20 PubMed DOI PMC
Kennedy Edward E, Bogerd Hal H, Kornepati Anand AR, et al. Posttranscriptional m6A editing of HIV-1 mRNAs enhances viral gene expression. Cell Host Microbe. 2016;19(5):675–685. doi: 10.1016/j.chom.2016.04.002 PubMed DOI PMC
Tirumuru N, Zhao BS, Lu W, et al. N6-methyladenosine of HIV-1 RNA regulates viral infection and HIV-1 gag protein expression. Elife. 2016;5. doi: 10.7554/eLife.15528 PubMed DOI PMC
Ringeard M, Marchand V, Decroly E, et al. FTSJ3 is an RNA 2'-O-methyltransferase recruited by HIV to avoid innate immune sensing. Nature. 2019;565(7740):500–504. doi: 10.1038/s41586-018-0841-4 PubMed DOI
Šimonová A, Svojanovská B, Trylčová J, et al. LC/MS analysis and deep sequencing reveal the accurate RNA composition in the HIV-1 virion. Sci Rep. 2019;9(1):8697. doi: 10.1038/s41598-019-45079-1 PubMed DOI PMC
Šimonová A, Romanská V, Benoni B, et al. Honeybee iflaviruses pack specific tRNA fragments from host cells in their virions. Chembiochem. 2022;23(17):e202200281. doi: 10.1002/cbic.202200281 PubMed DOI PMC
Navarro B, Flores R, Di Serio F. Advances in viroid-host interactions. Annu Rev Virol. 2021;8(1):305–325. doi: 10.1146/annurev-virology-091919-092331 PubMed DOI
Di Serio F, Torchetti EM, Daròs JA, et al. Reassessment of viroid RNA cytosine methylation status at the single nucleotide level. Viruses. 2019;11(4):11. doi: 10.3390/v11040357 PubMed DOI PMC
Domdey H, Jank P, Sänger L, et al. Studies on the primary and secondary structure of potato spindle tuber viroid: products of digestion with ribonuclease a and ribonuclease T1, and modification with bisulfite. Nucl Acids Res. 1978;5(4):1221–1236. doi: 10.1093/nar/5.4.1221 PubMed DOI PMC
Marquez-Molins J, Juarez-Gonzalez VT, Gomez G, et al. Occurrence of RNA post-transcriptional modifications in plant viruses and viroids and their correlation with structural and functional features. Virus Res. 2023;323:198958. doi: 10.1016/j.virusres.2022.198958 PubMed DOI PMC
Pallas V, Navarro A, Flores R. Isolation of a viroid-like RNA from hop different from hop stunt viroid. J Gener Virol. 1987;68:3201–3205.
Meyer KD, Saletore Y, Zumbo P et al. Comprehensive analysis of mRNA methylation reveals enrichment in 3' UTRs and near stop codons. Cell. 2012;149(7):1635–1646. doi: 10.1016/j.cell.2012.05.003 PubMed DOI PMC
Dominissini D, Moshitch-Moshkovitz S, Schwartz S, et al. Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq. Nature. 2012;485(7397):201. doi: 10.1038/nature11112 PubMed DOI
Linder B, Grozhik AV, Olarerin-George AO, et al. Single-nucleotide-resolution mapping of m6A and m6Am throughout the transcriptome. Nat Methods. 2015;12(8):767–772. doi: 10.1038/nmeth.3453 PubMed DOI PMC
Zhong Z-D, Xie Y-Y, Chen H-X, et al. Systematic comparison of tools used for m6A mapping from nanopore direct RNA sequencing. Nat Commun. 2023;14(1):1906. doi: 10.1038/s41467-023-37596-5 PubMed DOI PMC
Baquero-Pérez B, Yonchev ID, Delgado-Tejedor A, et al. N6-methyladenosine modification is not a general trait of viral RNA genomes. Nat Commun. 2024;15(1):1964. doi: 10.1038/s41467-024-46278-9 PubMed DOI PMC
Robinson JT, Thorvaldsdóttir H, Winckler W, et al. Integrative genomics viewer. Nat Biotechnol. 2011;29(1):24–26. doi: 10.1038/nbt.1754 PubMed DOI PMC
Abebe JS, Price AM, Hayer KE, et al. Drummer—rapid detection of RNA modifications through comparative nanopore sequencing. Bioinformat. 2022;38(11):3113–3115. doi: 10.1093/bioinformatics/btac274 PubMed DOI PMC
Pratanwanich PN, Yao F, Chen Y, et al. Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore. Nat Biotechnol. 2021;39(11):1394–1402. doi: 10.1038/s41587-021-00949-w PubMed DOI
Leger A, Amaral PP, Pandolfini L, et al. RNA modifications detection by comparative nanopore direct RNA sequencing. Nat Commun. 2021;12(1):7198. doi: 10.1038/s41467-021-27393-3 PubMed DOI PMC
Maestri S, Furlan M, Mulroney L, et al. Benchmarking of computational methods for m6A profiling with nanopore direct RNA sequencing. Brief Bioinform. 2024;25(2). doi: 10.1093/bib/bbae001 PubMed DOI PMC
Codoñer FM, Darós J-A, Solé RV, et al. The fittest versus the flattest: experimental confirmation of the quasispecies effect with subviral pathogens. PLOS Pathog. 2006;2(12):e136. doi: 10.1371/journal.ppat.0020136 PubMed DOI PMC
Parker MT, Knop K, Sherwood AV, et al. Nanopore direct RNA sequencing maps the complexity of Arabidopsis mRNA processing and m6A modification. Elife. 2020;9:e49658. doi: 10.7554/eLife.49658 PubMed DOI PMC
Xiao Y, Wang Y, Tang Q, et al. An elongation- and ligation-based qPCR amplification method for the radiolabeling-free detection of locus-specific N6-methyladenosine modification. Angew Chem Int Ed. 2018;57(49):15995–16000. doi: 10.1002/anie.201807942 PubMed DOI
Wang Y, Qu J, Ji S, et al. A land plant-specific transcription factor directly enhances transcription of a pathogenic noncoding RNA template by DNA-Dependent RNA polymerase II. Plant Cell. 2016;28(5):1094–1107. doi: 10.1105/tpc.16.00100 PubMed DOI PMC
Bojić T, Beeharry Y, Zhang DJ, et al. Tomato RNA polymerase II interacts with the rod-like conformation of the left terminal domain of the potato spindle tuber viroid positive RNA genome. J Gener Virol. 2012;93(7):1591–1600. doi: 10.1099/vir.0.041574-0 PubMed DOI
Shinde H, Dudhate A, Kadam US, et al. RNA methylation in plants: an overview. Front Plant Sci. 2023;14:14. doi: 10.3389/fpls.2023.1132959 PubMed DOI PMC
Manduzio S, Kang H. RNA methylation in chloroplasts or mitochondria in plants. RNA Biol. 2021;18(12):2127–2135. doi: 10.1080/15476286.2021.1909321 PubMed DOI PMC