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An m 6 A-YTH Module Controls Developmental Timing and Morphogenesis in Arabidopsis

https://doi.org/10.1105/tpc.17.00833

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What this work says

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inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102650openalex-snapshot

The m6A-YTH regulatory system in plants: A status

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110801openalex-snapshot

Analysis of N6-methyladenosine reveals a new important mechanism regulating the salt tolerance of sweet sorghum

inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111417openalex-snapshot

Tomato SlYTH1 encoding a putative RNA m6A reader affects plant growth and fruit shape

inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111546openalex-snapshot

The N6-methyladenosine binding proteins YTH03/05/10 coordinately regulate rice plant height

inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111570openalex-snapshot

The role of shoot-derived RNAs transported to plant root in response to abiotic stresses

inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111794openalex-snapshot

Analysis of N6-methyladenosine reveals a new important mechanism regulating the salt tolerance of sugar beet (Beta vulgaris)

inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111807openalex-snapshot

Knockout of SlYTH2, encoding a YTH domain-containing protein, caused plant dwarfing, delayed fruit internal ripening, and increased seed abortion rate in tomato

inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112023openalex-snapshot

N6-methyladenosine analysis unveils key mechanisms underlying long-term salt stress tolerance in switchgrass (Panicum virgatum)

inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112228openalex-snapshot

The knockout of SlMTC impacts tomato seed size and reduces resistance to salt stress in tomato

inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.10.007openalex-snapshot

Overexpression of watermelon m6A methyltransferase ClMTB enhances drought tolerance in tobacco by mitigating oxidative stress and photosynthesis inhibition and modulating stress-responsive gene expression

inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.04.031openalex-snapshot

Exploring epitranscriptomics for crop improvement and environmental stress tolerance

inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108255openalex-snapshot

ECT12, an YTH-domain protein, is a potential mRNA m6A reader that affects abiotic stress responses by modulating mRNA stability in Arabidopsis

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108781openalex-snapshot

Characterization of the m6A gene family in switchgrass and functional analysis of PvALKBH10 during flowering

inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110210openalex-snapshot

Genome-wide identification of the m6A gene family and analysis of m6A methylome in alfalfa under drought stress

inferred← citeshttps://doi.org/10.1016/j.plgene.2026.100576openalex-snapshot

The emerging role of the plant epitranscriptome in regulating development and stress responses

inferred← citeshttps://doi.org/10.1016/j.rhisph.2023.100745openalex-snapshot

Delineating host responses induced by Trichoderma in castor through comparative transcriptome analysis

inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113725openalex-snapshot

N6-methyladenosine RNA methylation is important for dormancy release in sweet cherry

inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.11.008openalex-snapshot

Composition and function of stress granules and P-bodies in plants

inferred← citeshttps://doi.org/10.1016/j.stress.2026.101245openalex-snapshot

Involvement of genomic variations and m6A modification in differential gene expression related to environmental responses: A subspecies-level study in plants

inferred← citeshttps://doi.org/10.1016/j.tplants.2019.01.005openalex-snapshot

Messenger RNA Modifications in Plants

inferred← citeshttps://doi.org/10.1016/j.tplants.2020.04.005openalex-snapshot

m6A Editing: New Tool to Improve Crop Quality?

inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.023openalex-snapshot

Coupling epigenetics and RNA polyadenylation: missing links

inferred← citeshttps://doi.org/10.1016/j.tplants.2024.11.012openalex-snapshot

Epitranscriptomic regulation through phase separation in plants

inferred← citeshttps://doi.org/10.1016/j.tplants.2026.08.011openalex-snapshot

Advances of N6-methyladenosine RNA methylation in tree species

inferred← citeshttps://doi.org/10.1016/j.virol.2024.110373openalex-snapshot

N6-methyladenosine (m6A) modification: Emerging regulators in plant-virus interactions

inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100546openalex-snapshot

Detection, regulation, and functions of RNA N6-methyladenosine modification in plants

inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101037openalex-snapshot

Crosstalk between RNA m6A modification and epigenetic factors in plant gene regulation

inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101043openalex-snapshot

Selective recognition of PTRE1 transcripts mediated by protein–protein interaction between the m6A reader ECT2 and PTRE1

inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101232openalex-snapshot

RNA modifications in plant biotic interactions

inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101789openalex-snapshot

Phytochrome B and the methyltransferase complex coordinately regulate N6-methyladenosine RNA modification and shade avoidance responses in Arabidopsis

inferred← citeshttps://doi.org/10.1016/j.ygeno.2022.110542openalex-snapshot

Transcriptome-wide profiling of mRNA N6-methyladenosine modification in rice panicles and flag leaves

inferred← citeshttps://doi.org/10.1021/acs.biochem.8b01166openalex-snapshot

The m 6 A Writer: Rise of a Machine for Growing Tasks

inferred← citeshttps://doi.org/10.1021/acs.jafc.4c04832openalex-snapshot

N 6 -Methyladenosine RNA Modification Regulates Maize Resistance to Maize Chlorotic Mottle Virus Infection

inferred← citeshttps://doi.org/10.1021/acs.jafc.5c00050openalex-snapshot

N6-Methyladenosine Modification Regulates Prunus Necrotic Ringspot Virus Infection in Cucumis sativus

inferred← citeshttps://doi.org/10.1038/s41419-021-03625-8openalex-snapshot

Linking the YTH domain to cancer: the importance of YTH family proteins in epigenetics

inferred← citeshttps://doi.org/10.1038/s41467-022-35146-zopenalex-snapshot

N6-methyladenosine RNA modification regulates photosynthesis during photodamage in plants

inferred← citeshttps://doi.org/10.1038/s41477-024-01638-7openalex-snapshot

N6-methyladenosine-mediated feedback regulation of abscisic acid perception via phase-separated ECT8 condensates in Arabidopsis

inferred← citeshttps://doi.org/10.1038/s41477-025-01945-7openalex-snapshot

NERD-dependent m6A modification of the nascent FLC transcript regulates flowering time in Arabidopsis

inferred← citeshttps://doi.org/10.1038/s41477-025-01947-5openalex-snapshot

RNA m6A modification meets plant hormones

inferred← citeshttps://doi.org/10.1038/s41477-025-02013-wopenalex-snapshot

Regulation of m6A RNA reader protein OsECT3 activity by lysine acetylation in the cold stress response in rice

inferred← citeshttps://doi.org/10.1038/s41477-025-02137-zopenalex-snapshot

RNA m6A regulates the transcription and heterochromatin state of retrotransposons in Arabidopsis

inferred← citeshttps://doi.org/10.1038/s41477-026-02299-4openalex-snapshot

CDS-localized m6A drives co-translational RNA decay to relieve biotic and abiotic endoplasmic reticulum stresses

inferred← citeshttps://doi.org/10.1038/s41587-021-00982-9openalex-snapshot

RNA demethylation increases the yield and biomass of rice and potato plants in field trials

inferred← citeshttps://doi.org/10.1038/s44318-024-00312-0openalex-snapshot

ALBA proteins facilitate cytoplasmic YTHDF-mediated reading of m6A in Arabidopsis

inferred← citeshttps://doi.org/10.1038/s44318-025-00662-3openalex-snapshot

Single-nucleotide m⁶A mapping uncovers redundant YTHDF function in planarian progenitor fate selection

inferred← citeshttps://doi.org/10.1042/ebc20200029openalex-snapshot

Processing of coding and non-coding RNAs in plant development and environmental responses

inferred← citeshttps://doi.org/10.1073/pnas.2003733117openalex-snapshot

mRNA adenosine methylase (MTA) deposits m 6 A on pri-miRNAs to modulate miRNA biogenesis in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1073/pnas.2405100121openalex-snapshot

The m 6 A reader SlYTH2 negatively regulates tomato fruit aroma by impeding the translation process

inferred← citeshttps://doi.org/10.1073/pnas.2411100121openalex-snapshot

m 6 A modification plays an integral role in mRNA stability and translation during pattern-triggered immunity

inferred← citeshttps://doi.org/10.1080/07388551.2020.1751059openalex-snapshot

Insights into the N6-methyladenosine mechanism and its functionality: progress and questions

inferred← citeshttps://doi.org/10.1080/15476286.2024.2399914openalex-snapshot

ECT2 peptide sequences outside the YTH domain regulate its m 6 A-RNA binding

inferred← citeshttps://doi.org/10.1080/15592294.2026.2733375openalex-snapshot

Decoding chromatin-associated RNA (caRNA) interaction networks: from genome-wide dynamic capture to epigenetic mechanisms in plants and animals

inferred← citeshttps://doi.org/10.1080/15592324.2022.2079308openalex-snapshot

N6-methyladenosine–modified RNA acts as a molecular glue that drives liquid–liquid phase separation in plants

inferred← citeshttps://doi.org/10.1093/bfgp/elaa021openalex-snapshot

The impact of epitranscriptomic marks on post-transcriptional regulation in plants

inferred← citeshttps://doi.org/10.1093/fqsafe/fyae050openalex-snapshot

Novel nomenclature and functional insights into YTH genes in the Rosaceae family

inferred← citeshttps://doi.org/10.1093/hr/uhad094openalex-snapshot

The m6A reader MhYTP2 regulates the stability of its target mRNAs contributing to low nitrogen tolerance in apple (Malus domestica)

inferred← citeshttps://doi.org/10.1093/hr/uhad284openalex-snapshot

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

inferred← citeshttps://doi.org/10.1093/hr/uhaf173openalex-snapshot

SlALKBH9B is involved in drought-induced flower drop by regulating ethylene production

inferred← citeshttps://doi.org/10.1093/jmcb/mjz085openalex-snapshot

Marking RNA: m6A writers, readers, and functions in Arabidopsis

inferred← citeshttps://doi.org/10.1093/jxb/erab074openalex-snapshot

Transcriptome-wide analysis of epitranscriptome and translational efficiency associated with heterosis in maize

inferred← citeshttps://doi.org/10.1093/jxb/erac461openalex-snapshot

ArabidopsisN6-methyladenosine methyltransferase FIONA1 regulates floral transition by affecting the splicing ofFLCand the stability of floral activatorsSPL3andSEP3

inferred← citeshttps://doi.org/10.1093/jxb/ery262openalex-snapshot

New insights into the plant epitranscriptome

inferred← citeshttps://doi.org/10.1093/pcp/pcz067openalex-snapshot

Transcription Is Just the Beginning of Gene Expression Regulation: The Functional Significance of RNA-Binding Proteins to Post-transcriptional Processes in Plants

inferred← citeshttps://doi.org/10.1093/plcell/koac345openalex-snapshot

Toward a systems view on RNA-binding proteins and associated RNAs in plants: Guilt by association

inferred← citeshttps://doi.org/10.1093/plcell/koac346openalex-snapshot

Beyond transcription: compelling open questions in plant RNA biology

inferred← citeshttps://doi.org/10.1093/plcell/koad044openalex-snapshot

The covalent nucleotide modifications within plant mRNAs: What we know, how we find them, and what should be done in the future

inferred← citeshttps://doi.org/10.1093/plcell/koad103openalex-snapshot

N6-methyladenosine RNA methylation modulates liquid‒liquid phase separation in plants

inferred← citeshttps://doi.org/10.1093/plcell/koad224openalex-snapshot

Pathogen-induced m6A dynamics affect plant immunity

inferred← citeshttps://doi.org/10.1093/plcell/koad300openalex-snapshot

The m6A reader ECT1 drives mRNA sequestration to dampen salicylic acid–dependent stress responses in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plcell/koae149openalex-snapshot

The m6A reader ECT8 is an abiotic stress sensor that accelerates mRNA decay in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plcell/koae156openalex-snapshot

Adding salt to the mix: The m6A reader ECT8 is a stress sensor, expediting mRNA decay in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plcell/koag064openalex-snapshot

SlYTH3 regulates tomato leaf senescence via recognition of N 6-methyladenosine–modified SlHDZIV2 transcripts

inferred← citeshttps://doi.org/10.1093/plcell/koag196openalex-snapshot

The mRNA covalent modification dihydrouridine regulates transcript turnover and photosynthetic capacity during plant abiotic stress

inferred← citeshttps://doi.org/10.1093/plcell/koag287openalex-snapshot

RNA m6A methylation fine-tunes the jasmonic acid biosynthesis pathway to modulate plant aging

inferred← citeshttps://doi.org/10.1093/plphys/kiab509openalex-snapshot

Unique features of mRNA m6A methylomes during expansion of tomato (Solanum lycopersicum) fruits

inferred← citeshttps://doi.org/10.1093/plphys/kiad112openalex-snapshot

m6A mRNA modification promotes chilling tolerance and modulates gene translation efficiency in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plphys/kiad470openalex-snapshot

Global hypermethylation of the N6-methyladenosine RNA modification associated with apple heterografting

inferred← citeshttps://doi.org/10.1093/plphys/kiae451openalex-snapshot

N6-methyladenosine transcriptome-wide profiles of maize kernel development

inferred← citeshttps://doi.org/10.1093/plphys/kiae529openalex-snapshot

An mRNA methylase and demethylase regulate sorghum salt tolerance by mediating N 6-methyladenosine modification

inferred← citeshttps://doi.org/10.1093/plphys/kiaf180openalex-snapshot

The N6-methyladenosine reader ECT1 regulates seed germination via gibberellic acid- and phytochrome B-mediated signaling

inferred← citeshttps://doi.org/10.1093/plphys/kiaf245openalex-snapshot

The m6A reader SlYTH1 regulates flavor-related volatiles biosynthesis via affecting mRNA stability and translation in tomato fruit

inferred← citeshttps://doi.org/10.1093/treephys/tpad074openalex-snapshot

Inhibition of DNA and RNA methylation disturbs root development of moso bamboo

inferred← citeshttps://doi.org/10.1101/2020.12.19.423605openalex-snapshot

Alternative promoter usage modulates miRNA-guided translation inhibition of a m 6 A reader in phosphate starvation

inferred← citeshttps://doi.org/10.1101/2021.04.18.440342openalex-snapshot

Principles of mRNA targeting via the Arabidopsis m 6 A-binding protein ECT2

inferred← citeshttps://doi.org/10.1101/2021.10.20.465108openalex-snapshot

hyperTRIBER: a flexible R package for the analysis of differential RNA editing

inferred← citeshttps://doi.org/10.1101/2022.01.24.477497openalex-snapshot

The m 6 A writer FIONA1 methylates the 3’UTR of FLC and controls flowering in Arabidopsis

inferred← citeshttps://doi.org/10.1101/2022.03.22.485398openalex-snapshot

Suppression of transposon mobilization by m 6 A-mediated RNA sequestration in stress granules

inferred← citeshttps://doi.org/10.1101/2023.01.17.524395openalex-snapshot

Light and temperature regulate m 6 A-RNA modification to regulate growth in plants

inferred← citeshttps://doi.org/10.1101/2024.06.06.597704openalex-snapshot

ALBA proteins facilitate cytoplasmic YTHDF-mediated reading of m 6 A in plants

inferred← citeshttps://doi.org/10.1101/2024.08.05.606563openalex-snapshot

ECT2 peptide sequences outside the YTH domain regulate its m 6 A-RNA binding

inferred← citeshttps://doi.org/10.1101/2025.05.22.655480openalex-snapshot

m6A RNA methylation attenuates thermotolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1101/2025.08.13.670251openalex-snapshot

RNA m 6 A Methylation Control Salt Response by Affecting Photosynthesis Capacity

inferred← citeshttps://doi.org/10.1104/pp.19.00323openalex-snapshot

Evolution of the RNA N6-Methyladenosine Methylome Mediated by Genomic Duplication

inferred← citeshttps://doi.org/10.1104/pp.19.00987openalex-snapshot

Natural Variation in RNA m 6 A Methylation and Its Relationship with Translational Status

inferred← citeshttps://doi.org/10.1104/pp.19.01156openalex-snapshot

Occurrence and Functions of m 6 A and Other Covalent Modifications in Plant mRNA

inferred← citeshttps://doi.org/10.1105/tpc.17.00854openalex-snapshot

The YTH Domain Protein ECT2 Is an m 6 A Reader Required for Normal Trichome Branching in Arabidopsis

inferred← citeshttps://doi.org/10.1105/tpc.18.00352openalex-snapshot

A Tale of Three Studies: Uncovering the Crucial Roles of m6A Readers

inferred← citeshttps://doi.org/10.1105/tpc.18.00456openalex-snapshot

The Story Continues: Following the Fate of m6A Marks in the Eukaryotic Transcriptome

inferred← citeshttps://doi.org/10.1105/tpc.19.00639openalex-snapshot

A Kinase and a Glycosylase Catabolize Pseudouridine in the Peroxisome to Prevent Toxic Pseudouridine Monophosphate Accumulation

inferred← citeshttps://doi.org/10.1111/jipb.12917openalex-snapshot

H3K36me2 is highly correlated with m6A modifications in plants

inferred← citeshttps://doi.org/10.1111/jipb.13152openalex-snapshot

Phase separation in plants: New insights into cellular compartmentalization

inferred← citeshttps://doi.org/10.1111/jipb.13394openalex-snapshot

The RNA N6‐methyladenosine demethylase ALKBH9B modulates ABA responses in Arabidopsis

inferred← citeshttps://doi.org/10.1111/jipb.13575openalex-snapshot

The m6A reader SiYTH1 enhances drought tolerance by affecting the messenger RNA stability of genes related to stomatal closure and reactive oxygen species scavenging in Setaria italica

inferred← citeshttps://doi.org/10.1111/jipb.13781openalex-snapshot

Reading m6A marks in mRNA: A potent mechanism of gene regulation in plants

inferred← citeshttps://doi.org/10.1111/jpi.70109openalex-snapshot

Comprehensive Genome‐Wide Identification and Expression Analysis of the N6‐Methyladenosine (m6A) Regulatory Network Influences Rapid Stress Adaptation With Exogenous Melatonin in Rice

inferred← citeshttps://doi.org/10.1111/mec.70553openalex-snapshot

Polyphenism Through RNA Chemical Modifications

inferred← citeshttps://doi.org/10.1111/mpp.13097openalex-snapshot

RNA N 6 ‐methyladenosine modification suppresses replication of rice black streaked dwarf virus and is associated with virus persistence in its insect vector

inferred← citeshttps://doi.org/10.1111/nph.16283openalex-snapshot

Glandular trichomes: micro‐organs with model status?

inferred← citeshttps://doi.org/10.1111/nph.16660openalex-snapshot

The m6A reader ECT2 post‐transcriptionally regulates proteasome activity in Arabidopsis

inferred← citeshttps://doi.org/10.1111/nph.18117openalex-snapshot

MTA1‐mediated RNA m 6 A modification regulates autophagy and is required for infection of the rice blast fungus

inferred← citeshttps://doi.org/10.1111/nph.18583openalex-snapshot

The blue light receptor CRY1 interacts with FIP37 to promote N 6 ‐methyladenosine RNA modification and photomorphogenesis in Arabidopsis

inferred← citeshttps://doi.org/10.1111/nph.19568openalex-snapshot

Dynamic N6 ‐methyladenosine RNA modification regulates peanut resistance to bacterial wilt

inferred← citeshttps://doi.org/10.1111/nph.19976openalex-snapshot

m6 A demethylase O s ALKBH 5 is required for double‐strand break formation and repair by affecting m RNA stability in rice meiosis

inferred← citeshttps://doi.org/10.1111/nph.20008openalex-snapshot

Dynamic m6A mRNA methylation reveals the involvement of AcALKBH10 in ripening‐related quality regulation in kiwifruit

inferred← citeshttps://doi.org/10.1111/nph.20227openalex-snapshot

mRNA ADENOSINE METHYLASE promotes drought tolerance through N 6 ‐methyladenosine‐dependent and independent impacts on mRNA regulation in Arabidopsis

inferred← citeshttps://doi.org/10.1111/nph.70473openalex-snapshot

The m6A writer complex function in main stem apex development by promoting mRNA stability of GIF3, HDA6, and KNAT2/6 in Gossypium hirsutum

inferred← citeshttps://doi.org/10.1111/pbi.13149openalex-snapshot

N6‐methyladenosine regulatory machinery in plants: composition, function and evolution

inferred← citeshttps://doi.org/10.1111/pbi.13733openalex-snapshot

The m6A reader MhYTP2 regulates MdMLO19 mRNA stability and antioxidant genes translation efficiency conferring powdery mildew resistance in apple

inferred← citeshttps://doi.org/10.1111/pbi.13792openalex-snapshot

m6A‐mediated regulation of crop development and stress responses

inferred← citeshttps://doi.org/10.1111/pbi.13829openalex-snapshot

The plant epitranscriptome: revisiting pseudouridine and 2′‐ O ‐methyl RNA modifications

inferred← citeshttps://doi.org/10.1111/pbi.13913openalex-snapshot

Epitranscriptomic mRNA modifications governing plant stress responses: underlying mechanism and potential application

inferred← citeshttps://doi.org/10.1111/pbi.14036openalex-snapshot

N6 ‐methyladenosine RNA modification regulates cotton drought response in a Ca2+ and ABA ‐dependent manner

inferred← citeshttps://doi.org/10.1111/pbi.70226openalex-snapshot

N6 ‐methyladenosine RNA modification regulates light intensity‐dependent terpenoid biosynthesis in Schizonepeta tenuifolia

inferred← citeshttps://doi.org/10.1111/pce.14447openalex-snapshot

ALKBH9C, a potential RNA m 6 A demethylase, regulates the response of Arabidopsis to abiotic stresses and abscisic acid

inferred← citeshttps://doi.org/10.1111/pce.14807openalex-snapshot

FIONA1‐mediated mRNA m 6 A methylation regulates the response of Arabidopsis to salt stress

inferred← citeshttps://doi.org/10.1111/pce.15494openalex-snapshot

The RNA m 6 A Methyltransferase PheMTA1 and PheMTA2 of Moso Bamboo Regulate Root Development and Resistance to Salt Stress in Plant

inferred← citeshttps://doi.org/10.1111/ppl.13505openalex-snapshot

Alpha‐ketoglutarate‐dependent dioxygenase homolog 10B, an N 6 ‐methyladenosine mRNA demethylase, plays a role in salt stress and abscisic acid responses in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1111/ppl.70135openalex-snapshot

ECT8 , an mRNA m 6 A reader, enhances salt stress tolerance by modulating mRNA stability in Arabidopsis

inferred← citeshttps://doi.org/10.1111/tpj.14193openalex-snapshot

Kernel size‐related genes revealed by an integrated eQTL analysis during early maize kernel development

inferred← citeshttps://doi.org/10.1111/tpj.14589openalex-snapshot

Topologies of N6‐adenosine methylation (m6A) in land plant mitochondria and their putative effects on organellar gene expression

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