Exploring N6-methyladenosine (m6A) modification in tree species: opportunities and challenges

Muthusamy Ramakrishnan , K. Shanmugha Rajan , Sileesh Mullasseri , Zishan Ahmad , Mingbing Zhou , Anket Sharma , Subbiah Ramasamy , Qiang Wei

Horticulture Research ›› 2024, Vol. 11 ›› Issue (2) : 284

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Horticulture Research ›› 2024, Vol. 11 ›› Issue (2) :284 DOI: 10.1093/hr/uhad284
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Exploring N6-methyladenosine (m6A) modification in tree species: opportunities and challenges
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Abstract

N6-methyladenosine (m6A) in eukaryotes is the most common and widespread internal modification in mRNA. The modification regulates mRNA stability, translation efficiency, and splicing, thereby fine-tuning gene regulation. In plants, m6A is dynamic and critical for various growth stages, embryonic development, morphogenesis, flowering, stress response, crop yield, and biomass. Although recent high-throughput sequencing approaches have enabled the rapid identification of m6A modification sites, the site-specific mechanism of this modification remains unclear in trees. In this review, we discuss the functional significance of m6A in trees under different stress conditions and discuss recent advancements in the quantification of m6A. Quantitative and functional insights into the dynamic aspect of m6A modification could assist researchers in engineering tree crops for better productivity and resistance to various stress conditions.

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Muthusamy Ramakrishnan, K. Shanmugha Rajan, Sileesh Mullasseri, Zishan Ahmad, Mingbing Zhou, Anket Sharma, Subbiah Ramasamy, Qiang Wei. Exploring N6-methyladenosine (m6A) modification in tree species: opportunities and challenges. Horticulture Research, 2024, 11 (2) : 284 DOI:10.1093/hr/uhad284

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Acknowledgements

The authors wish to thank the anonymous reviewers for their valuable time and insightful comments, which greatly improved the quality of the manuscript. We apologize to those whose original work(s) could not be included in this review owing to space limitations.

Preparation of this review was supported by a grant from the National Key Research & Development Program of China (2021YFD2200503-01), a grant from the National Natural Science Foundation of China (32071848), a grant from the Natural Science Foundation of Jiangsu Province (BK20231289), the Jiangxi ‘Shuangqian’ Program (S2019DQKJ2030), the Natural Science Foundation for Distinguished Young Scholars of Nanjing Forestry University (JC2019004), the Project for Groundbreaking Achievements of Nanjing Forestry University (202211), and a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions. The authors are also grateful for the Young Foreign Talent Program (QN2022014012L) and the support of Metasequoia Faculty Research Start-up Funding (163100028) at the Bamboo Research Institute, Nanjing Forestry University, for the first author, M.R. K.S.R. is supported by the Dean of Faculty Fellowship, the Koshland Prize, and a Sir Charles Clore Postdoctoral Fellowship from the Weizmann Institute.

Author contributions

M.R., K.S.R., Q.W., and S.M. planned, designed and wrote the review. M.R., K.S.R., Q.W., and M.Z. outlined and edited the review. M.R., S.M., and K.S.R. drew the images. M.R. and Q.W. made the tables. M.R., K.S.R., M.Z., A.S., Z.A., S.R., and Q.W. edited and revised the review.

Data availability

No additional data were generated or are associated with this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

Liang Z, Riaz A, Chachar S. et al. Epigenetic modifications of mRNA and DNA in plants. Mol Plant. 2020; 13:14-30

[2]

Hu J, Cai J, Xu T. et al. Epitranscriptomic mRNA modifications governing plant stress responses: underlying mechanism and potential application. Plant Biotechnol J. 2022; 20:2245-57

[3]

Shi H, Wei J, He C. Where, when, and how: context-dependent functions of RNA methylation writers, readers, and erasers. Mol Cell. 2019; 74:640-50

[4]

Yang X, Hu X, Liu J. et al. N6-methyladenine modification in non-coding RNAs and its function in cancer. Biomark Res. 2020; 8:61

[5]

Ontiveros RJ, Stoute J, Liu KF. The chemical diversity of RNA modifications. Biochem J. 2019; 476:1227-45

[6]

Wiener D, Schwartz S. The epitranscriptome beyond m6A. Nat Rev Genet. 2021; 22:119-31

[7]

Wilkinson E, Cui YH, He YY. Context-dependent roles of RNA modifications in stress responses and diseases. Int J Mol Sci. 2021; 22:1949

[8]

Desrosiers R, Friderici K, Rottman F. Identification of methylated nucleosides in messenger RNA from Novikoff hepatoma cells. Proc Natl Acad Sci USA. 1974; 71:3971-5

[9]

Shen L, Liang Z, Wong CE. et al. Messenger RNA modifications in plants. Trends Plant Sci. 2019; 24:328-41

[10]

Wang L, Zhuang H, Fan W. et al. m6A RNA methylation impairs gene expression variability and reproductive thermotolerance in Arabidopsis. Genome Biol. 2022; 23:244

[11]

Bhat SS, Bielewicz D, Gulanicz T. et al. mRNA adenosine methylase (MTA) deposits m6A on pri-miRNAs to modulate miRNA biogenesis in Arabidopsis thaliana. Proc Natl Acad Sci USA. 2020; 117:21785-95

[12]

Kadumuri RV, Janga SC. Epitranscriptomic code and its alterations in human disease. Trends Mol Med. 2018; 24:886-903

[13]

Xu Y, Song M, Hong Z. et al. The N6-methyladenosine METTL 3 regulates tumorigenesis and glycolysis by mediating m6A methylation of the tumor suppressor LATS1 in breast cancer. J Exp Clin Cancer Res. 2023; 42:10

[14]

Duan HC, Wei LH, Zhang C. et al. ALKBH10B is an RNA N6-methyladenosine demethylase affecting Arabidopsis floral transition. Plant Cell. 2017; 29:2995-3011

[15]

Arribas-Hernández L, Bressendorff S, Hansen MH. et al. An m6A-YTH module controls developmental timing and morphogenesis in Arabidopsis. Plant Cell. 2018; 30:952-67

[16]

Scutenaire J, Deragon J-M, Jean V. et al. The YTH domain protein ECT2 is an m6A reader required for normal trichome branching in Arabidopsis. Plant Cell. 2018; 30:986-1005

[17]

Ramakrishnan M, Rajan KS, Mullasseri S. et al. The plant epitranscriptome: revisiting pseudouridine and 2′-O-methyl RNA modifications. Plant Biotechnol J. 2022; 20:1241-56

[18]

Ye T, Wang J, Zhao H. et al. Role of N6-methyladenosine in the pathogenesis, diagnosis and treatment of pancreatic cancer (review). Int J Oncol. 2023; 62:4

[19]

Li T, Wang H, Zhang Y. et al. Comprehensive profiling of epigenetic modifications in fast-growing Moso bamboo shoots. Plant Physiol. 2022; 191:1017-35

[20]

Bhat SS, Bielewicz D, Jarmolowski A. et al. N6-methyladenosine (m6A): revisiting the old with focus on new, an Arabidopsis thaliana centered review. Genes (Basel). 2018; 9:596

[21]

Reichel M, Köster T, Staiger D. Marking RNA: m6A writers, readers, and functions in Arabidopsis. J Mol Cell Biol. 2019; 11:899-910

[22]

Martínez-Pérez M, Aparicio F, López-Gresa MP. et al. Arabidopsis m6A demethylase activity modulates viral infection of a plant virus and the m6A abundance in its genomic RNAs. Proc Natl Acad Sci USA. 2017; 114:10755-60

[23]

Liufu Y, Xi F, Wu L. et al. Inhibition of DNA and RNA methylation disturbs root development of moso bamboo. Tree Physiol. 2023; 43:1653-74

[24]

Hou N, Li C, He J. et al. MdMTA-mediated m6A modification enhances drought tolerance by promoting mRNA stability and translation efficiency of genes involved in lignin deposition and oxidative stress. New Phytol. 2022; 234:1294-314

[25]

Zhang W, Qian Y, Jia G. The detection and functions of RNA modification m6A based on m6A writers and erasers. J Biol Chem. 2021; 297:100973

[26]

Bokar JA, Rath-Shambaugh ME, Ludwiczak R. et al. Characterization and partial purification of mRNA N6-adenosine methyltransferase from HeLa cell nuclei. Internal mRNA methylation requires a multisubunit complex. J Biol Chem. 1994; 269:17697-704

[27]

Knuckles P, Bühler M. Adenosine methylation as a molecular imprint defining the fate of RNA. FEBS Lett. 2018; 592:2845-59

[28]

Zhong S, Li H, Bodi Z. et al. MTA is an Arabidopsis messenger RNA adenosine methylase and interacts with a homolog of a sex-specific splicing factor. Plant Cell. 2008; 20:1278-88

[29]

Ruzicka K, Zhang M, Campilho A. et al. Identification of factors required for m6A mRNA methylation in Arabidopsis reveals a role for the conserved E3 ubiquitin ligase HAKAI. New Phytol. 2017; 215:157-72

[30]

Shen L, Liang Z, Gu X. et al. N6-methyladenosine RNA modification regulates shoot stem cell fate in Arabidopsis. Dev Cell. 2016; 38:186-200

[31]

Ma K, Han J, Zhang Z. et al. OsEDM2L mediates m6A of EAT1 transcript for proper alternative splicing and polyadenylation regulating rice tapetal degradation. J Integr Plant Biol. 2021; 63:1982-94

[32]

Hu J, Cai J, Park SJ. et al. N6-methyladenosine mRNA methylation is important for salt stress tolerance in Arabidopsis. Plant J. 2021; 106:1759-75

[33]

Lu L, Zhang Y, He Q. et al. MTA, an RNA m6A methyltransferase, enhances drought tolerance by regulating the development of trichomes and roots in poplar. Int J Mol Sci. 2020; 21:2462

[34]

Hu J, Manduzio S, Kang H. Epitranscriptomic RNA methylation in plant development and abiotic stress responses. Front Plant Sci. 2019; 10:500

[35]

Dominissini D, Nachtergaele S, Moshitch-Moshkovitz S. et al. The dynamic N1-methyladenosine methylome in eukaryotic messenger RNA. Nature. 2016; 530:441-6

[36]

Arguello AE, DeLiberto AN, Kleiner RE. RNA chemical proteomics reveals the N6-methyladenosine (m6A)-regulated protein-RNA interactome. J Am Chem Soc. 2017; 139:17249-52

[37]

Dai XY, Shi L, Li Z. et al. Main N6-methyladenosine readers: YTH family proteins in cancers. Front. Oncol. 2021; 11:635329

[38]

Yue H, Nie X, Yan Z. et al. N6-methyladenosine regulatory machinery in plants: composition,function and evolution. Plant Biotechnol J. 2019; 17:1194-208

[39]

Wang N, Guo T, Sun X. et al. Functions of two Malus hupehensis (Pamp.) Rehd. YTPs (MhYTP1 and MhYTP2) in biotic- and abiotic-stress responses. Plant Sci. 2017; 261:18-27

[40]

Zhou Y, Hu L, Jiang L. et al. Genome-wide identification and expression analysis of YTH domain-containing RNA-binding protein family in cucumber (Cucumis sativus). Genes Genomics. 2018; 40:579-89

[41]

Zhou C, Wang C, Liu H. et al. Identification and analysis of adenine N6-methylation sites in the rice genome. Nature Plants. 2018; 4:554-63

[42]

Wei LH, Song P, Wang Y. et al. The m6A reader ECT2 controls trichome morphology by affecting mRNA stability in Arabidopsis. Plant Cell. 2018; 30:968-85

[43]

Wu J, Peled-Zehavi H, Galili G. The m6A reader ECT2 post-transcriptionally regulates proteasome activity in Arabidopsis. New Phytol. 2020; 228:151-62

[44]

Ok SH, Jeong HJ, Bae JM. et al. Novel CIPK1-associated proteins in Arabidopsis contain an evolutionarily conserved C-terminal region that mediates nuclear localization. Plant Phys-iol. 2005; 139:138-50

[45]

Guo T, Liu C, Meng F. et al. The m6A reader MhYTP2 regulates MdMLO19 mRNA stability and antioxidant genes translation efficiency conferring powdery mildew resistance in apple. Plant Biotechnol J. 2022; 20:511-25

[46]

Liu C, Guo T, Wang N. et al. Overexpression of MhYTP2 enhances apple water-use efficiency by activating ABA and ethylene signaling. Environ Exp Bot. 2019; 157:260-8

[47]

Wang N, Guo T, Wang P. et al. Functional analysis of apple MhYTP1 and MhYTP2 genes in leaf senescence and fruit ripening. Sci Hortic. 2017; 221:23-32

[48]

Sun X, Wu W, Yang Y. et al. Genome-wide identification of m6A writers, erasers and readers in poplar 84K. Genes (Basel). 2022; 13:1018

[49]

Wang W, Huang Q, Liao Z. et al. ALKBH5 prevents hepatocellular carcinoma progression by post-transcriptional inhibition of PAQR4 in an m6A dependent manner. Exp. Hematol Oncol. 2023; 12:1

[50]

Jia G, Fu Y, Zhao X. et al. N6-methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO. Nat Chem Biol. 2011; 7:885-7

[51]

Yu Q, Liu S, Yu L. et al. RNA demethylation increases the yield and biomass of rice and potato plants in field trials. Nat Biotechnol. 2021; 39:1581-8

[52]

Alemu EA, He C, Klungland A. ALKBHs-facilitated RNA modifications and de-modifications. DNA Repair (Amst). 2016; 44:87-91

[53]

Scarrow M, Chen N, Sun G. Insights into the N6-methyladenosine mechanism and its functionality: progress and questions. Crit Rev Biotechnol. 2020; 40:639-52

[54]

Shoaib Y, Hu J, Manduzio S. et al. Alpha-ketoglutarate-dependent dioxygenase homolog 10B, an N6-methyladenosine mRNA demethylase, plays a role in salt stress and abscisic acid responses in Arabidopsis thaliana. Physiol Plant. 2021; 173:1078-89

[55]

Tang J, Yang J, Duan H. et al. ALKBH10B, an mRNA m6A demethylase, modulates ABA response during seed germination in Arabidopsis. Front. Plant Sci. 2021; 12:712713

[56]

Martínez-Pérez M, Gómez-Mena C, Alvarado-Marchena L. et al. The m6A RNA demethylase ALKBH9B plays a critical role for vascular movement of alfalfa mosaic virus in Arabidopsis. Front Microbiol. 2021; 12:745576

[57]

Zhang G, Lv Z, Diao S. et al. Unique features of the m6A methylome and its response to drought stress in sea buckthorn (Hippophae rhamnoides Linn.). RNA Biol. 2021; 18:794-803

[58]

Gao Y, Liu X, Jin Y. et al. Drought induces epitranscriptome and proteome changes in stem-differentiating xylem of Populus trichocarpa. Plant Physiol. 2022; 190:459-79

[59]

Zhang Y, Wang J, Ma W. et al. Transcriptome-wide m6A methylation in natural yellow leaf of Catalpa fargesii. Front. Plant Sci. 2023; 14:1167789

[60]

Yin S, Chen Y, Chen Y. et al. Genome-wide profiling of rice double-stranded RNA-binding protein 1-associated RNAs by targeted RNA editing. Plant Physiol. 2023; 192:805-20

[61]

McMahon AC, Rahman R, Jin H. et al. TRIBE: hijacking an RNA-editing enzyme to identify cell-specific targets of RNA-binding proteins. Cell. 2016; 165:742-53

[62]

Rahman R, Xu W, Jin H. et al. Identification of RNA-binding protein targets with HyperTRIBE. Nat Protoc. 2018; 13:1829-49

[63]

Xu W, Rahman R, Rosbash M. Mechanistic implications of enhanced editing by a HyperTRIBE RNA-binding protein. RNA. 2018; 24:173-82

[64]

Arribas-Hernández L, Rennie S, Schon M. et al. The YTHDF proteins ECT2 and ECT3 bind largely overlapping target sets and influence target mRNA abundance, not alternative polyadenylation. elife. 2021; 10:e72377

[65]

Zhou G, Niu R, Zhou Y. et al. Proximity editing to identify RNAs in phase-separated RNA binding protein condensates. Cell Discov. 2021; 7:72

[66]

Murakami S, Jaffrey SR. Hidden codes in mRNA: control of gene expression by m6A. Mol Cell. 2022; 82:2236-51

[67]

Wang S, Lv W, Li T. et al. Dynamic regulation and functions of mRNA m6A modification. Cancer Cell Int. 2022; 22:48

[68]

Huang Q, Mo J, Liao Z. et al. The RNA m6A writer WTAP in diseases: structure, roles, and mechanisms. Cell Death Dis. 2022; 13:852

[69]

Luo G-Z, MacQueen A, Zheng G. et al. Unique features of the m6A methylome in Arabidopsis thaliana. Nat Commun. 2014; 5:5630

[70]

Arribas-Hernández L, Brodersen P. Occurrence and functions of m6A and other covalent modifications in plant mRNA. Plant Physiol. 2019; 182:79-96

[71]

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

[72]

Choi J, Ieong KW, Demirci H. et al. N6-methyladenosine in mRNA disrupts tRNA selection and translation-elongation dynamics. Nat Struct Mol Biol. 2016; 23:110-5

[73]

Zhao BS, Roundtree IA, He C. Post-transcriptional gene regulation by mRNA modifications. Nat Rev Mol Cell Biol. 2017; 18:31-42

[74]

Zhou J, Wan J, Gao X. et al. Dynamic m6A mRNA methylation directs translational control of heat shock response. Nature. 2015; 526:591-4

[75]

Xu T, Wu X, Wong CE. et al. FIONA1-mediated m6A modification regulates the floral transition in Arabidopsis. Adv Sci. 2022; 9:e2103628

[76]

Liang Z, Zhang L, Chen H. et al. m6A-maize: weakly supervised prediction of m6A-carrying transcripts and m6A-affecting mutations in maize (Zea mays). Methods. 2022; 203:226-32

[77]

Huang T, He W-J, Li C. et al. Transcriptome-wide analyses of RNA m6A methylation in hexaploid wheat reveal its roles in mRNA translation regulation. Front. Plant Sci. 2022; 13:917335

[78]

Cheng Q, Wang P, Wu G. et al. Coordination of m6A mRNA methylation and gene transcriptome in rice response to cadmium stress. Rice. 2021; 14:62

[79]

Mao X, Hou N, Liu Z. et al. Profiling of N6-methyladenosine (m6A) modification landscape in response to drought stress in apple (Malus prunifolia (Willd.) Borkh). Plants. 2022; 11:103

[80]

Zhu C, Zhang S, Zhou C. et al. Genome-wide investigation of N6-methyladenosine regulatory genes and their roles in tea (Camellia sinensis) leaves during withering process. Front. Plant Sci. 2021; 12:702303

[81]

Tian Y, Zeng J, Fan R. Comprehensive analysis of N6-methyladenosine regulatory genes from Citrus grandis and expression profilings in the fruits of “Huajuhong” (C. grandis “Tomentosa”) during various development stages. Horticulturae. 2022; 8:462

[82]

Wang Y, Wang H, Xi F. et al. Profiling of circular RNA N6-methyladenosine in moso bamboo (Phyllostachys edulis) using nanopore-based direct RNA sequencing. J Integr Plant Biol. 2020; 62:1823-38

[83]

Wang W, Li W, Cheng Z. et al. Transcriptome-wide N6-methyladenosine profiling of cotton root provides insights for salt stress tolerance. Environ Exp Bot. 2022; 194:104729

[84]

Anderson SJ, Kramer MC, Gosai SJ. et al. N6-methyladenosine inhibits local ribonucleolytic cleavage to stabilize mRNAs in Arabidopsis. Cell Rep. 2018; 25:1146-1157.e3

[85]

Kramer MC, Janssen KA, Palos K. et al. N6-methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis. Plant. Direct. 2020; 4:e00239

[86]

Ma W, Cui S, Lu Z. et al. YTH domain proteins play an essential role in rice growth and stress response. Plants (Basel). 2022; 11:2206

[87]

Chen M, Guo L, Ramakrishnan M. et al. Rapid growth of Moso bamboo (Phyllostachys edulis): cellular roadmaps, transcriptome dynamics, and environmental factors. Plant Cell. 2022; 34:3577-610

[88]

Janssen KA, Xie Y, Kramer MC. et al. Data-independent acquisition for the detection of mononucleoside RNA modifications by mass spectrometry. J Am Soc Mass Spectrom. 2022; 33:885-93

[89]

Tuncel G, Kalkan R. Importance of mN6-methyladenosine (m6A) RNA modification in cancer. Med Oncol. 2019; 36:36

[90]

Zhang Y, Lu L, Li X. Detection technologies for RNA modifications. Exp Mol Med. 2022; 54:1601-16

[91]

Richter F, Plehn JE, Bessler L. et al. RNA marker modifications reveal the necessity for rigorous preparation protocols to avoid artifacts in epitranscriptomic analysis. Nucleic Acids Res. 2022; 50:4201-15

[92]

Peer E, Rechavi G, Dominissini D. Epitranscriptomics: regulation of mRNA metabolism through modifications. Curr Opin Chem Biol. 2017; 41:93-8

[93]

Thüring K, Schmid K, Keller P. et al. LC-MS analysis of methylated RNA. Methods Mol Biol. 2017; 1562:3-18

[94]

Zheng H-x, Zhang X-s, Sui N. Advances in the profiling of N6-methyladenosine (m6A) modifications. Biotechnol Adv. 2020; 45:107656

[95]

Helm M, Motorin Y. Detecting RNA modifications in the epitranscriptome: predict and validate. Nat Rev Genet. 2017; 18:275-91

[96]

Sarkar A, Gasperi W, Begley U. et al. Detecting the epitranscriptome. Wiley Interdiscip Rev. RNA. 2021; 12:e1663

[97]

Jora M, Lobue PA, Ross RL. et al. Detection of ribonucleoside modifications by liquid chromatography coupled with mass spectrometry. Biochim Biophys Acta Gene Regul Mech. 2019; 1862:280-90

[98]

Limbach PA, Paulines MJ. Going global: the new era of mapping modifications in RNA. Wiley Interdiscip Rev RNA. 2017; 8:e1367

[99]

Liu N, Parisien M, Dai Q. et al. Probing N6-methyladenosine RNA modification status at single nucleotide resolution in mRNA and long noncoding RNA. RNA. 2013; 19:1848-56

[100]

Imanishi M, Tsuji S, Suda A. et al. Detection of N6-methyladenosine based on the methyl-sensitivity of MazF RNA endonuclease. Chem Commun (Camb). 2017; 53:12930-3

[101]

Garcia-Campos MA, Edelheit S, Toth U. et al. Deciphering the “m6A code” via antibody-independent quantitative profiling. Cell. 2019; 178:731-747.e16

[102]

Zhang Z, Chen LQ, Zhao YL. et al. Single-base mapping of m6A by an antibody-independent method. Sci Adv. 2019;5:eaax0250

[103]

Stephenson W, Razaghi R, Busan S. et al. Direct detection of RNA modifications and structure using single-molecule nanopore sequencing. Cell Genom. 2022; 2:100097

[104]

Begik O, Lucas MC, Pryszcz LP. et al. Quantitative profiling of pseudouridylation dynamics in native RNAs with nanopore sequencing. Nat Biotechnol. 2021; 39:1278-91

[105]

Furlan M, Delgado-Tejedor A, Mulroney L. et al. Computational methods for RNA modification detection from nanopore direct RNA sequencing data. RNA Biol. 2021; 18:31-40

[106]

Leger A, Amaral PP, Pandolfini L. et al. RNA modifications detection by comparative nanopore direct RNA sequencing. Nat Commun. 2021; 12:7198

[107]

Wan YK, Hendra C, Pratanwanich PN. et al. Beyond sequencing: machine learning algorithms extract biology hidden in Nanopore signal data. Trends Genet. 2022; 38:246-57

[108]

Hendra C, Pratanwanich PN, Wan YK. et al. Detection of m6A from direct RNA sequencing using a multiple instance learning framework. Nat Methods. 2022; 19:1590-8

[109]

Liu H, Begik O, Lucas MC. et al. Accurate detection of m6A RNA modifications in native RNA sequences. Nat Commun. 2019; 10:4079

[110]

Liu H, Begik O, Novoa EM. EpiNano: detection of m6A RNA modifications using Oxford Nanopore direct RNA sequencing. Methods Mol Biol. 2021; 2298:31-52

[111]

Lorenz DA, Einstein JM. et al. Sathe S, Direct RNA sequencing enables m6A detection in endogenous transcript isoforms at base-specific resolution. RNA. 2020; 26:19-28

[112]

Gao Y, Liu X, Wu B. et al. Quantitative profiling of N6-methyladenosine at single-base resolution in stem-differentiating xylem of Populus trichocarpa using nanopore direct RNA sequencing. Genome Biol. 2021; 22:22

[113]

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; 14:1906

[114]

Cottilli P, Itoh Y, Nobe Y. et al. Cryo-EM structure and rRNA modification sites of a plant ribosome. Plant Commun. 2022; 3:100342

[115]

Li Y, Tollefsbol TO. DNA methylation detection: bisulfite genomic sequencing analysis. Methods Mol Biol. 2011; 791:11-21

[116]

Werner S, Galliot A, Pichot F. et al. NOseq: amplicon sequencing evaluation method for RNA m6A sites after chemical deamination. Nucleic Acids Res. 2021; 49:e23

[117]

Liu C, Sun H, Yi Y. et al. Absolute quantification of single-base m6A methylation in the mammalian transcriptome using GLORI. Nat Biotechnol. 2022; 41:355-66

[118]

Jones JD, Eyler DE, Koutmou KS. Mapping mRNA modifications for functional studies. Nat Biotechnol. 2022; 41:324-5

[119]

Xiao Y-L, Liu S, Ge R. et al. Transcriptome-wide profiling and quantification of N6-methyladenosine by enzyme-assisted adenosine deamination. Nat Biotechnol. 2023; 41:993-1003

[120]

Ma J, Zhang L, Chen S. et al. A brief review of RNA modification related database resources. Methods. 2022; 203:342-53

[121]

Boccaletto P, Stefaniak F, Ray A. et al. MODOMICS: a database of RNA modification pathways 2021 update. Nucleic Acids Res. 2022;50:D231-5

[122]

Liu Q, Gregory RI. RNAmod: an integrated system for the annotation of mRNA modifications. Nucleic Acids Res. 2019;47:W548-55

[123]

Cantara WA, Crain PF, Rozenski J. et al. The RNA modification database, RNAMDB: 2011 update. Nucleic Acids Res. 2011;39:D195-201

[124]

Luo X, Li H, Liang J. et al. RMVar: an updated database of functional variants involved in RNA modifications. Nucleic Acids Res. 2021;49:D1405-12

[125]

Nie F, Feng P, Song X. et al. RNAWRE: a resource of writers, readers and erasers of RNA modifications. Database (Oxford). 2020;2020:baaa049

[126]

Deng S, Zhang H, Zhu K. et al. M6A2Target: a comprehensive database for targets of m6A writers, erasers and readers. Brief Bioinform. 2021;22:bbaa055

[127]

Xuan J-J, Sun W-J, Lin P-H. et al. RMBase v2.0: deciphering the map of RNA modifications from epitranscriptome sequencing data. Nucleic Acids Res. 2018;46:D327-34

[128]

Liu S, Zhu A, He C. et al.REPIC:a database for exploring the N6-methyladenosine methylome. Genome Biol. 2020; 21:100

[129]

Tang Y, Chen K, Song B. et al. m6A-atlas: a comprehensive knowledgebase for unraveling the N6-methyladenosine (m6A) epitranscriptome. Nucleic Acids Res. 2021;49:D134-43

[130]

Zhang Y, Jiang J, Ma J. et al. DirectRMDB: a database of post-transcriptional RNA modifications unveiled from direct RNA sequencing technology Nucleic Acids Res. 2023;51:D106-16

[131]

Douglas CJ. Populus as a model tree in comparative and evolutionary genomics of angiosperm trees. In: Groover A, Cronk Q, Switzerland, Springer International Publishing,eds. Plant Genetics and Genomics: Crops and Models, Vol. 21. Cham, 2017, 61-84

[132]

Jansson S, Douglas CJ. Populus: a model system for plant biology. Annu Rev Plant Biol. 2007; 58:435-58

[133]

Taylor G. Populus: Arabidopsis for forestry. Do we need a model tree? Ann Bot. 2002; 90:681-9

[134]

Uzonyi A, Dierks D, Nir R. et al. Exclusion of m6A from splice-site proximal regions by the exon junction complex dictates m6A topologies and mRNA stability. Mol Cell. 2023; 83:237-251.e7

[135]

Kan RL, Chen J, Sallam T. Crosstalk between epitranscriptomic and epigenetic mechanisms in gene regulation. Trends Genet. 2022; 38:182-93

[136]

Zhou L, Gao G, Tang R. et al. m6A-mediated regulation of crop development and stress responses. Plant Biotechnol J. 2022; 20:1447-55

[137]

Jiménez-Ramírez IA, Pijeira-Fernández G, Moreno-Cálix DM. et al. Same modification, different location: the mythical role of N6-adenine methylation in plant genomes. Planta. 2022; 256:9

[138]

Yue J, Wei Y, Zhao M. The reversible methylation of m6A is involved in plant virus infection. Biology (Basel). 2022; 11:271

[139]

Yao H, Yang Y, Yang YG. scDART-seq: mapping m6A at the single-cell level. Mol Cell. 2022; 82:713-5

[140]

Motorin Y, Helm M. RNA nucleotide methylation: 2021 update. Wiley Interdiscip Rev RNA. 2021; 13:e1691

[141]

Moshitch-Moshkovitz S, Dominissini D, Rechavi G. The epitranscriptome toolbox. Cell. 2022; 185:764-76

[142]

Krusnauskas R, Stakaitis R, Steponaitis G. et al. Identification and comparison of m6A modifications in glioblastoma non-coding RNAs with MeRIP-seq and Nanopore dRNA-seq. Epige-netics. 2023; 18:2163365

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