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Characterization of METTL16 as a cytoplasmic RNA binding protein

https://doi.org/10.1371/journal.pone.0227647
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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U6 snRNA Maturation and Stability
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Newly synthesized small nuclear RNAs appear transiently in the cytoplasm
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Comprehensive Analysis of mRNA Methylation Reveals Enrichment in 3′ UTRs and near Stop Codons
inferredcites →https://doi.org/10.1016/j.cell.2015.05.014openalex-snapshot
N6-methyladenosine Modulates Messenger RNA Translation Efficiency
inferredcites →https://doi.org/10.1016/j.cell.2015.08.011openalex-snapshot
HNRNPA2B1 Is a Mediator of m6A-Dependent Nuclear RNA Processing Events
inferredcites →https://doi.org/10.1016/j.cell.2015.11.015openalex-snapshot
High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities
inferredcites →https://doi.org/10.1016/j.cell.2017.05.003openalex-snapshot
The U6 snRNA m 6 A Methyltransferase METTL16 Regulates SAM Synthetase Intron Retention
inferredcites →https://doi.org/10.1016/j.celrep.2014.05.048openalex-snapshot
Perturbation of m6A Writers Reveals Two Distinct Classes of mRNA Methylation at Internal and 5′ Sites
inferredcites →https://doi.org/10.1016/j.celrep.2017.02.059openalex-snapshot
m6A RNA Methylation Regulates the Self-Renewal and Tumorigenesis of Glioblastoma Stem Cells
inferredcites →https://doi.org/10.1016/j.celrep.2017.11.092openalex-snapshot
S-Adenosylmethionine Synthesis Is Regulated by Selective N6-Adenosine Methylation and mRNA Degradation Involving METTL16 and YTHDC1
inferredcites →https://doi.org/10.1016/j.molcel.2016.03.021openalex-snapshot
The m 6 A Methyltransferase METTL3 Promotes Translation in Human Cancer Cells
inferredcites →https://doi.org/10.1016/j.molcel.2018.07.025openalex-snapshot
Structural Basis for Regulation of METTL16, an S-Adenosylmethionine Homeostasis Factor
inferredcites →https://doi.org/10.1016/j.molcel.2018.08.004openalex-snapshot
Methylation of Structured RNA by the m6A Writer METTL16 Is Essential for Mouse Embryonic Development
inferredcites →https://doi.org/10.1016/j.stem.2015.09.005openalex-snapshot
Coordination of m 6 A mRNA Methylation and Gene Transcription by ZFP217 Regulates Pluripotency and Reprogramming
inferredcites →https://doi.org/10.1016/j.tig.2016.03.006openalex-snapshot
Nuclear m 6 A Reader YTHDC1 Regulates mRNA Splicing
inferredcites →https://doi.org/10.1038/cr.2014.3openalex-snapshot
Mammalian WTAP is a regulatory subunit of the RNA N6-methyladenosine methyltransferase
inferredcites →https://doi.org/10.1038/cr.2017.10openalex-snapshot
Cytoplasmic m6A reader YTHDF3 promotes mRNA translation
inferredcites →https://doi.org/10.1038/cr.2017.15openalex-snapshot
YTHDF3 facilitates translation and decay of N6-methyladenosine-modified RNA
inferredcites →https://doi.org/10.1038/nature12730openalex-snapshot
N6-methyladenosine-dependent regulation of messenger RNA stability
inferredcites →https://doi.org/10.1038/nature14234openalex-snapshot
N6-methyladenosine-dependent RNA structural switches regulate RNA–protein interactions
inferredcites →https://doi.org/10.1038/nature19342openalex-snapshot
m6A RNA methylation promotes XIST-mediated transcriptional repression
inferredcites →https://doi.org/10.1038/nature24678openalex-snapshot
Promoter-bound METTL3 maintains myeloid leukaemia by m6A-dependent translation control
inferredcites →https://doi.org/10.1038/ncomms12626openalex-snapshot
YTHDF2 destabilizes m6A-containing RNA through direct recruitment of the CCR4–NOT deadenylase complex
inferredcites →https://doi.org/10.1038/nrm.2016.132openalex-snapshot
Post-transcriptional gene regulation by mRNA modifications
inferredcites →https://doi.org/10.1038/s41589-018-0184-3openalex-snapshot
N6-Methyladenosine methyltransferase ZCCHC4 mediates ribosomal RNA methylation
inferredcites →https://doi.org/10.1038/s41598-018-23608-8openalex-snapshot
Structural insights into the RNA methyltransferase domain of METTL16
inferredcites →https://doi.org/10.1073/pnas.1602883113openalex-snapshot
Hypoxia induces the breast cancer stem cell phenotype by HIF-dependent and ALKBH5-mediated m 6 A-demethylation of NANOG mRNA
inferredcites →https://doi.org/10.1073/pnas.1614759113openalex-snapshot
Methyltransferase-like protein 16 binds the 3′-terminal triple helix of MALAT1 long noncoding RNA
inferredcites →https://doi.org/10.1073/pnas.1618558114openalex-snapshot
Climate variation drives dengue dynamics
inferredcites →https://doi.org/10.1089/scd.2016.0062openalex-snapshot
N 6 -Methyladenosine Methyltransferases and Demethylases: New Regulators of Stem Cell Pluripotency and Differentiation
inferredcites →https://doi.org/10.1093/nar/gkz619openalex-snapshot
The human 18S rRNA m6A methyltransferase METTL5 is stabilized by TRMT112
inferredcites →https://doi.org/10.1097/00008469-199311000-00011openalex-snapshot
The MCF10 family of spontaneously immortalized human breast epithelial cell lines
inferredcites →https://doi.org/10.1101/gad.262766.115openalex-snapshot
RNA N 6 -methyladenosine methylation in post-transcriptional gene expression regulation
inferredcites →https://doi.org/10.1101/gad.4.12b.2264openalex-snapshot
Multiple roles for U6 snRNA in the splicing pathway.
inferredcites →https://doi.org/10.1126/science.1149185openalex-snapshot
Profiling Essential Genes in Human Mammary Cells by Multiplex RNAi Screening
inferredcites →https://doi.org/10.1126/science.aac7041openalex-snapshot
Identification and characterization of essential genes in the human genome
inferredcites →https://doi.org/10.1126/science.aac7557openalex-snapshot
Gene essentiality and synthetic lethality in haploid human cells
inferredcites →https://doi.org/10.1128/mcb.00302-17openalex-snapshot
A High-Resolution Genome-Wide CRISPR/Cas9 Viability Screen Reveals Structural Features and Contextual Diversity of the Human Cell-Essential Proteome
inferredcites →https://doi.org/10.1128/mcb.00815-09openalex-snapshot
A Role for Dynein in the Inhibition of Germ Cell Proliferative Fate
inferredcites →https://doi.org/10.1186/s13059-015-0609-1openalex-snapshot
Fate by RNA methylation: m6A steers stem cell pluripotency
inferredcites →https://doi.org/10.1186/s13073-016-0395-8openalex-snapshot
Emerging links between m6A and misregulated mRNA methylation in cancer
inferredcites →https://doi.org/10.1261/rna.061044.117openalex-snapshot
N 6 -methyladenosine is required for the hypoxic stabilization of specific mRNAs
inferredcites →https://doi.org/10.15252/embr.201744940openalex-snapshot
Human METTL16 is a N6‐methyladenosine (m6A) methyltransferase that targets pre‐mRNAs and various non‐coding RNAs
inferredcites →https://doi.org/10.16288/j.yczz.16-049openalex-snapshot
RNA epigenetic modification: N6-methyladenosine.
inferredcites →https://doi.org/10.18632/oncotarget.11743openalex-snapshot
Hypoxia-inducible factors regulate pluripotency factor expression by ZNF217- and ALKBH5-mediated modulation of RNA methylation in breast cancer cells
inferredcites →https://doi.org/10.18632/oncotarget.25782openalex-snapshot
N6-methyladenosine contributes to cellular phenotype in a genetically-defined model of breast cancer progression
inferredcites →https://doi.org/10.2174/1389203716666150901113553openalex-snapshot
Structural and Functional Characterization of the Proteins Responsible for N6-Methyladenosine Modification and Recognition

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/bies.202200236openalex-snapshot
Regulation and function of poised mRNAs in lymphocytes
inferred← citeshttps://doi.org/10.1002/ijc.35067openalex-snapshot
The m6A ‐independent role of epitranscriptomic factors in cancer
inferred← citeshttps://doi.org/10.1002/wrna.1681openalex-snapshot
RNA methyltransferase METTL16 : Targets and function
inferred← citeshttps://doi.org/10.1002/wrna.1810openalex-snapshot
Ghost authors revealed: The structure and function of human N6 ‐methyladenosine RNA methyltransferases
inferred← citeshttps://doi.org/10.1002/wrna.70004openalex-snapshot
Epitranscriptome‐Mediated Regulation of Neuronal Translation
inferred← citeshttps://doi.org/10.1007/978-3-030-71612-7_12openalex-snapshot
From m6A to Cap-Adjacent m6Am and their Effects on mRNAs
inferred← citeshttps://doi.org/10.1007/s12035-024-04532-7openalex-snapshot
Multi-Omics Approach Reveals Genes and Pathways Affected in Miller-Dieker Syndrome
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The epitranscriptome: RNA modifications in vascular remodelling
inferred← citeshttps://doi.org/10.1016/j.bcp.2020.114258openalex-snapshot
N6-methyladenosine RNA modification in cancer therapeutic resistance: Current status and perspectives
inferred← citeshttps://doi.org/10.1016/j.canlet.2025.217698openalex-snapshot
RNA methyltransferase METTL16: From molecular mechanisms to therapeutic prospects in cancers
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112150openalex-snapshot
METTL16 Promotes Translation and Lung Tumorigenesis by Sequestering Cytoplasmic eIF4E2
inferred← citeshttps://doi.org/10.1016/j.dci.2023.104713openalex-snapshot
METTL16, an evolutionarily conserved m6A methyltransferase member, inhibits the antiviral immune response of miiuy croaker (Miichthys miiuy)
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117518openalex-snapshot
METTL16 controls airway inflammations in smoking-induced COPD via regulating glutamine metabolism
inferred← citeshttps://doi.org/10.1016/j.gendis.2025.101758openalex-snapshot
METTL16 in cancer: Roles and regulatory mechanisms
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127710openalex-snapshot
m6A methyltransferase AflIme4 orchestrates mycelial growth, development and aflatoxin B1 biosynthesis in Aspergillus flavus
inferred← citeshttps://doi.org/10.1016/j.psj.2024.104384openalex-snapshot
METTL16 inhibits differentiation and promotes proliferation and slow myofibers formation in chicken myoblasts
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2021.05.006openalex-snapshot
Relevance of N6-methyladenosine regulators for transcriptome: Implications for development and the cardiovascular system
inferred← citeshttps://doi.org/10.1016/j.ymeth.2022.06.007openalex-snapshot
Sequence-specific targeting of RNA
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c01247openalex-snapshot
Methyl-Transferase-Like Protein 16 (METTL16): The Intriguing Journey of a Key Epitranscriptomic Player Becoming an Emerging Biological Target
inferred← citeshttps://doi.org/10.1038/s12276-020-0407-zopenalex-snapshot
The emerging role of RNA modifications in the regulation of mRNA stability
inferred← citeshttps://doi.org/10.1038/s41420-022-01050-0openalex-snapshot
The emerging roles of N6-methyladenosine (m6A)-modified long non-coding RNAs in human cancers
inferred← citeshttps://doi.org/10.1038/s41467-023-42832-zopenalex-snapshot
MePMe-seq: antibody-free simultaneous m6A and m5C mapping in mRNA by metabolic propargyl labeling and sequencing
inferred← citeshttps://doi.org/10.1038/s41585-023-00851-xopenalex-snapshot
RNA N6-methyladenosine modifications in urological cancers: from mechanism to application
inferred← citeshttps://doi.org/10.1038/s41598-022-08616-zopenalex-snapshot
Transcriptome-wide analysis of glioma stem cell specific m6A modifications in long-non-coding RNAs
inferred← citeshttps://doi.org/10.1080/15476286.2021.2002003openalex-snapshot
Up–to–date on the evidence linking miRNA-related epitranscriptomic modifications and disease settings. Can these modifications affect cross-kingdom regulation?
inferred← citeshttps://doi.org/10.1093/cvr/cvab160openalex-snapshot
mRNA modifications in cardiovascular biology and disease: with a focus on m6A modification
inferred← citeshttps://doi.org/10.1093/jas/skac034openalex-snapshot
Function of m6A and its regulation of domesticated animals’ complex traits
inferred← citeshttps://doi.org/10.1093/molbev/msab267openalex-snapshot
Evolution of Methyltransferase-Like (METTL) Proteins in Metazoa: A Complex Gene Family Involved in Epitranscriptomic Regulation and Other Epigenetic Processes
inferred← citeshttps://doi.org/10.1093/nar/gkab378openalex-snapshot
A comprehensive review of m6A/m6Am RNA methyltransferase structures
inferred← citeshttps://doi.org/10.1093/nar/gkab900openalex-snapshot
The comprehensive interactomes of human adenosine RNA methyltransferases and demethylases reveal distinct functional and regulatory features
inferred← citeshttps://doi.org/10.1111/bjh.19722openalex-snapshot
Thrombopoietin improves the functions of bone marrow endothelial progenitor cells via METTL16 /Akt signalling of haematological patients with chemotherapy‐induced thrombocytopenia
inferred← citeshttps://doi.org/10.1111/tpj.70537openalex-snapshot
Dynamics of N 6 ‐methyladenosine ( m6A ) under salt stress in poplar and the intrinsic mechanism by which METTL4 ( PagMTC ) enhances salt tolerance
inferred← citeshttps://doi.org/10.1186/s12967-021-02918-yopenalex-snapshot
Potential roles of N6-methyladenosine (m6A) in immune cells
inferred← citeshttps://doi.org/10.1186/s13008-025-00152-2openalex-snapshot
METTL16/IGF2BP2 axis enhances malignant progression and DDP resistance through up-regulating COL4A1 by mediating the m6A methylation modification of LAMA4 in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1186/s13059-024-03332-5openalex-snapshot
N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.1186/s13578-020-00513-0openalex-snapshot
Biological functions of m6A methyltransferases
inferred← citeshttps://doi.org/10.1186/s40001-023-01382-2openalex-snapshot
The emerging roles of N6-methyladenosine RNA modifications in thyroid cancer
inferred← citeshttps://doi.org/10.1261/rna.079192.122openalex-snapshot
The catalytic-dead Pcif1 regulates gene expression and fertility inDrosophila
inferred← citeshttps://doi.org/10.1261/rna.079695.123openalex-snapshot
Functional analysis of 3′-UTR hairpins supports a two-tiered model for posttranscriptional regulation ofMAT2Aby METTL16
inferred← citeshttps://doi.org/10.1371/journal.pone.0306043openalex-snapshot
METTL16 participates in haemoglobin H disease through m6A modification
inferred← citeshttps://doi.org/10.18632/aging.206210openalex-snapshot
Pan-cancer analysis of Methyltransferase-like 16 (METTL16) and validated in colorectal cancer
inferred← citeshttps://doi.org/10.20944/preprints202011.0402.v1openalex-snapshot
From m6A to Cap-Adjacent m6Am and Their Effects on mRNAs
inferred← citeshttps://doi.org/10.2174/1568009621666210127092828openalex-snapshot
The Role of RNA Modifications and RNA-modifying Proteins in Cancer Therapy and Drug Resistance
inferred← citeshttps://doi.org/10.29271/jcpsp.2022.12.1576openalex-snapshot
Clinical Significance of Methyltransferase-like 16 Expression in Epithelial Ovarian Cancer
inferred← citeshttps://doi.org/10.3389/fcell.2023.1157797openalex-snapshot
New insights on the interplays between m6A modifications and microRNA or lncRNA in gastrointestinal cancers
inferred← citeshttps://doi.org/10.3389/fmicb.2021.749171openalex-snapshot
LncRNA-ENST00000421645 Upregulates Kank1 to Inhibit IFN-γ Expression and Promote T Cell Apoptosis in Neurosyphilis
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1572976openalex-snapshot
Effects of m6A methylation of MAT2A mRNA regulated by METTL16 on learning and memory, hippocampal synaptic plasticity and Aβ1–42 in 5 × FAD mice
inferred← citeshttps://doi.org/10.3389/fncel.2022.820378openalex-snapshot
RNA N6-Methyladenosine Modifications and Its Roles in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fonc.2021.743990openalex-snapshot
N6-Methyladenosine-Sculpted Regulatory Landscape of Noncoding RNA
inferred← citeshttps://doi.org/10.3389/fonc.2026.1744928openalex-snapshot
The methyltransferase METTL16 in digestive system cancers: functions and mechanisms
inferred← citeshttps://doi.org/10.3390/biology13060391openalex-snapshot
RNA Binding by the m6A Methyltransferases METTL16 and METTL3
inferred← citeshttps://doi.org/10.3390/cancers15041232openalex-snapshot
Understanding the Epitranscriptome for Avant-Garde Brain Tumour Diagnostics
inferred← citeshttps://doi.org/10.3390/cimb45070346openalex-snapshot
RNA Methyltransferase METTL16’s Protein Domains Have Differential Functional Effects on Cell Processes
inferred← citeshttps://doi.org/10.3390/diagnostics12122996openalex-snapshot
N6-methyladenosine Modification of Noncoding RNAs: Mechanisms and Clinical Applications in Cancer
inferred← citeshttps://doi.org/10.3390/genes13122312openalex-snapshot
The Role of the m6A RNA Methyltransferase METTL16 in Gene Expression and SAM Homeostasis
inferred← citeshttps://doi.org/10.3390/ijms21218139openalex-snapshot
The Distinct Function and Localization of METTL3/METTL14 and METTL16 Enzymes in Cardiomyocytes
inferred← citeshttps://doi.org/10.3390/ijms22042176openalex-snapshot
METTL16, Methyltransferase-Like Protein 16: Current Insights into Structure and Function
inferred← citeshttps://doi.org/10.3390/ijms22116166openalex-snapshot
Long Non-Coding RNA Epigenetics
inferred← citeshttps://doi.org/10.3390/ijms23031057openalex-snapshot
N-6-Methyladenosine in Vasoactive microRNAs during Hypoxia; A Novel Role for METTL4
inferred← citeshttps://doi.org/10.3390/life11070669openalex-snapshot
Localization of METTL16 at the Nuclear Periphery and the Nucleolus Is Cell Cycle-Specific and METTL16 Interacts with Several Nucleolar Proteins
inferred← citeshttps://doi.org/10.3390/plants12030624openalex-snapshot
Current Insights into m6A RNA Methylation and Its Emerging Role in Plant Circadian Clock
inferred← citeshttps://doi.org/10.3390/v16040601openalex-snapshot
m6A Methylation in Regulation of Antiviral Innate Immunity
inferred← citeshttps://doi.org/10.6084/m9.figshare.26339943openalex-snapshot
Additional file 1 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26340166openalex-snapshot
Additional file 2 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751784openalex-snapshot
Additional file 3 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751787openalex-snapshot
Additional file 4 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751790openalex-snapshot
Additional file 5 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751793openalex-snapshot
Additional file 6 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751796openalex-snapshot
Additional file 7 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751799openalex-snapshot
Additional file 8 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751802openalex-snapshot
Additional file 9 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751805openalex-snapshot
Additional file 10 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751808openalex-snapshot
Additional file 11 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751811openalex-snapshot
Additional file 12 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751814openalex-snapshot
Additional file 13 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26751817openalex-snapshot
Additional file 14 of N6-methyladenosine writer METTL16-mediated alternative splicing and translation control are essential for murine spermatogenesis
inferred← citeshttps://doi.org/10.70675/73fb7d4ez0e4az4eafzbce9z244d7edb23e5openalex-snapshot
Exploration structurale de la maturation des ARN
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