| 2018 |
VIRMA (KIAA1429) is a component of the m6A methyltransferase complex (METTL3/METTL14/WTAP/VIRMA/HAKAI/ZC3H13) and mediates preferential m6A mRNA methylation in 3'UTR and near stop codon by recruiting the catalytic core components METTL3/METTL14/WTAP to guide region-selective methylations. VIRMA also associates with polyadenylation cleavage factors CPSF5 and CPSF6 in an RNA-dependent manner, and its depletion induces 3'UTR lengthening of several hundred mRNAs overlapping with METTL3 targets. |
Biochemical purification of m6A methyltransferase complex, RIP-seq, meRIP-seq, knockdown with RNA-seq, Co-IP |
Cell discovery |
High |
29507755
|
| 2018 |
VIRMA depletion and METTL3 depletion both induce 3'UTR lengthening of overlapping mRNA targets (>50% in common), linking VIRMA-guided m6A deposition to alternative polyadenylation control. |
siRNA knockdown, RNA-seq, 3'UTR length analysis |
Cell discovery |
High |
29507755
|
| 2019 |
KIAA1429 induces m6A methylation on the 3'UTR of GATA3 pre-mRNA, leading to displacement of the RNA-binding protein HuR and degradation of GATA3 pre-mRNA in hepatocellular carcinoma cells. A lncRNA GATA3-AS acts as a cis-acting element facilitating preferential KIAA1429 interaction with GATA3 pre-mRNA. |
MeRIP-seq, RIP-seq, RNA-seq, siRNA knockdown, mRNA stability assay |
Molecular cancer |
High |
31856849
|
| 2019 |
KIAA1429 regulates CDK1 expression in breast cancer in an m6A-independent manner, as identified by RNA immunoprecipitation sequencing and functional rescue experiments. |
RIP-seq, siRNA knockdown, rescue experiment, in vivo xenograft |
Oncogene |
Medium |
31285549
|
| 2019 |
KIAA1429 upregulates m6A modification of ID2 mRNA, inhibiting ID2 expression and thereby facilitating hepatocellular carcinoma migration and invasion. |
MeRIP-PCR, siRNA knockdown, transwell assays |
OncoTargets and therapy |
Low |
31118692
|
| 2020 |
Oocyte-specific deletion of Kiaa1429 in mice decreases m6A levels in oocytes, impairs germinal vesicle breakdown and meiosis resumption, alters RNA metabolism, and primarily affects alternative splicing of genes associated with oogenesis, demonstrating an in vivo role for VIRMA-mediated m6A in folliculogenesis. |
Conditional knockout mouse, RNA-seq, m6A quantification, splice analysis |
Cell death and differentiation |
High |
32094512
|
| 2020 |
VIRMA knockdown in prostate cancer cells decreases global m6A levels, attenuates malignant phenotype, and reduces stability and abundance of oncogenic lncRNAs CCAT1 and CCAT2, as shown by actinomycin D RNA stability assays and m6A/RNA co-immunoprecipitation. |
siRNA knockdown, ELISA for m6A, actinomycin D stability assay, RNA co-IP |
Cancers |
Medium |
32218194
|
| 2020 |
KIAA1429 regulates c-Jun mRNA stability in gastric cancer in an m6A-independent manner, as shown by RIP assay and luciferase reporter, with c-Jun overexpression rescuing KIAA1429 knockdown-induced proliferation inhibition. |
RNA-seq, RIP assay, luciferase assay, rescue experiment |
Journal of cellular physiology |
Medium |
32052427
|
| 2021 |
KIAA1429-mediated m6A modification of CHST11 mRNA recruits YTHDF2 to reduce CHST11 stability and expression, leading to inactivation of Hippo-YAP signaling in diffuse large B-cell lymphoma. |
CRISPR/Cas9 KO, RNA-seq, MeRIP-seq, RIP assay, luciferase assay, RNA stability assay, Co-IP |
Cellular & molecular biology letters |
High |
37076815
|
| 2021 |
VIRMA-mediated m6A modifications promote NSCLC progression via YTHDF2/3-dependent degradation of DAPK3 mRNA. Inhibition of DAPK3 rescued the tumor-suppressive phenotypes caused by VIRMA deficiency. |
siRNA knockdown, MeRIP-seq, RIP, rescue experiments, in vivo xenograft |
Cancer letters |
Medium |
34520821
|
| 2021 |
KIAA1429 promotes breast cancer metastasis by directly binding to the 3'UTR of SMC1A mRNA and enhancing its stability (m6A-independent), and SMC1A then promotes SNAIL transcription to drive EMT. |
siRNA knockdown, RIP assay, m6A-independent mechanism validation, in vivo nude mouse model |
Molecular therapy. Nucleic acids |
Medium |
34976433
|
| 2021 |
KIAA1429 and ALKBH5 oppositely regulate maturation of pri-miR-143-3p through m6A modification, with KIAA1429-mediated m6A enhancing pri-miR-143-3p processing by interaction with the microprocessor protein DGCR8, thereby regulating downstream target DDX6 and aortic dissection progression. |
Gain/loss-of-function, m6A sequencing, DGCR8 interaction assay, in vivo AngII model |
Frontiers in cell and developmental biology |
Medium |
34490238
|
| 2021 |
CRISPR/Cas9-mediated knockdown of VIRMA in germ cell tumor cells disrupts the remaining methyltransferase complex and decreases global m6A abundance, increases sensitivity to cisplatin through enhanced DNA damage (higher γH2AX and GADD45B levels) and downregulation of DNA repair factors XLF and MRE11. |
CRISPR/Cas9 KD, m6A quantification, western blot for DNA damage markers, chorioallantoic membrane in vivo assay |
Journal of experimental & clinical cancer research : CR |
High |
34446080
|
| 2021 |
m6A transferase KIAA1429 catalyzes m6A modification on LINC00958 loci, and LINC00958 then interacts with GLUT1 mRNA in an m6A-dependent manner to enhance GLUT1 mRNA stability and promote aerobic glycolysis in gastric cancer. |
MeRIP-seq, RIP assay, RNA stability assay, siRNA knockdown |
IUBMB life |
Medium |
34409730
|
| 2022 |
KIAA1429 regulates BTG2 expression in an m6A-YTHDF2-dependent manner in lung adenocarcinoma: KIAA1429 knockdown decreases m6A levels of BTG2 mRNA, leading to enhanced YTHDF2-dependent BTG2 mRNA stability and increased BTG2 expression, suppressing tumorigenesis. |
MeRIP-seq, RNA-seq, m6A dot blot, RIP, RNA stability assay |
Cancer communications |
High |
35730068
|
| 2022 |
KIAA1429 activates the JNK/MAPK pathway in lung adenocarcinoma by positively regulating MAP3K2 expression in an m6A methylation-dependent manner, promoting tumorigenesis and gefitinib resistance. |
siRNA knockdown, MeRIP, RNA-seq, in vivo xenograft, JNK/MAPK inhibitor assays |
Drug resistance updates |
Medium |
36493511
|
| 2022 |
KIAA1429 promotes gastric cancer cisplatin resistance by stabilizing FOXM1 mRNA through YTHDF1-mediated m6A modification at the 3'UTR of FOXM1. p65 (NF-κB) was shown by ChIP to bind the KIAA1429 promoter and regulate its expression. |
shRNA knockdown, ChIP assay, RIP, m6A quantification, RNA stability assay, in vivo xenograft |
Cancers |
Medium |
36291811
|
| 2022 |
KIAA1429 increases SIRT1 expression via regulating its mRNA stability in an m6A-dependent manner in colorectal cancer, promoting tumor growth and motility. |
shRNA knockdown, RNA stability assay, in vivo xenograft |
Cell death discovery |
Low |
35217651
|
| 2022 |
KIAA1429 increases HK2 mRNA stability in colorectal cancer by binding the m6A site of HK2 mRNA in an m6A-independent manner, promoting aerobic glycolysis and carcinogenesis. |
siRNA knockdown, RIP, RNA stability assay |
Bioengineered |
Low |
35546050
|
| 2022 |
KIAA1429 regulates alternative splicing profiles in hepatocellular carcinoma cells, with KIAA1429-bound transcripts (from RIP-seq) highly overlapping with regulated alternative splicing genes enriched in cell cycle and apoptosis pathways. |
RNA-seq, RIP-seq, multi-omics integration, clinical specimen validation |
Frontiers in oncology |
Medium |
36505780
|
| 2022 |
USP29 mediates deubiquitination to stabilize KIAA1429 protein levels, and KIAA1429 in turn promotes SOX8 mRNA stability through m6A modification in colorectal cancer, as confirmed by Co-IP. |
Co-IP, siRNA knockdown, CCK-8, colony formation, EdU, in vivo xenograft |
Biomolecules & biomedicine |
Medium |
36373629
|
| 2023 |
KIAA1429/VIRMA is mislocalized to the cytosol in breast cancer tissues and cell lines. The nuclear-enriched full-length VIRMA isoform (but not cytoplasmic N-terminal VIRMA) promotes m6A-dependent breast tumorigenesis. VIRMA overexpression upregulates m6A-modified NEAT1 lncRNA and enriches m6A on transcripts regulating the unfolded protein response (UPR), making cells more susceptible to death under stress. |
Isoform-specific overexpression, in vitro and in vivo tumorigenic assays, m6A profiling, subcellular fractionation |
Cellular and molecular life sciences : CMLS |
High |
37208522
|
| 2023 |
KIAA1429/VIRMA binds to the m6A-dependent RNA-binding protein IGF2BP3, leading to recruitment and stabilization of m6A-modified HAS2 mRNA in breast cancer, promoting cancer growth. KIAA1429/VIRMA is mislocalized to the cytosol in breast cancer. |
shRNA knockdown, RIP, RNA stability assay, Co-IP/pulldown for VIRMA-IGF2BP3 interaction, subcellular fractionation |
EMBO reports |
High |
37705505
|
| 2023 |
VIRMA mediates m6A methylation of E2F7 3'UTR, then IGF2BP2 binds and maintains E2F7 mRNA stability in nasopharyngeal carcinoma, driving E2F7-mediated transcription of ITGA2, ITGA5, and NTRK1 via cooperation with CBFB-RUNX1. |
Comprehensive m6A sequencing, RIP, RNA stability assay, high-throughput sequencing, in vitro and in vivo models |
The Journal of biological chemistry |
High |
37028765
|
| 2023 |
KIAA1429 negatively regulates tumor suppressor RND3 by decreasing its mRNA stability in coordination with the m6A reader YTHDC1, facilitating HCC metastasis. KIAA1429 regulates RND3 m6A modification via its RNA binding domain. |
RNA-seq, MeRIP-seq, RIP, MeRIP-qPCR, luciferase assay, RNA stability assay |
Cancer letters |
Medium |
38224863
|
| 2023 |
KIAA1429 promotes gastric cancer progression by destabilizing RASD1 mRNA in an m6A-YTHDF2-dependent manner; knockdown decreases m6A levels of RASD1 mRNA, enhancing YTHDF2-dependent RASD1 mRNA stability paradoxically (i.e., YTHDF2 here mediates degradation when KIAA1429 is active, shown by MeRIP-seq, RIP, and RNA stability assays). |
MeRIP-seq, RNA-seq, MeRIP-qPCR, dual luciferase assay, RNA stability assay, RIP, RNA pull-down |
Journal of translational medicine |
High |
38902717
|
| 2023 |
VIRMA stabilizes TMED2 and PARD3B mRNA in intrahepatic cholangiocarcinoma via m6A modification recognized by the m6A reader HuR (not YTHDF proteins), promoting ICC proliferation and metastasis through Akt/GSK/β-catenin and MEK/ERK/Slug signaling pathways. High VIRMA expression in ICC is driven by demethylation of H3K27me3 at the VIRMA promoter. |
RNA-seq, MeRIP-seq, SLAM-seq, RIP, luciferase reporter, ChIP assay, in vitro/in vivo ICC models |
Journal of gastroenterology |
High |
37391589
|
| 2023 |
HNRNPC recognizes VIRMA-installed m6A modification on TFAP2A mRNA, promoting TFAP2A expression and thereby DDR1 transcription in breast cancer, enhancing collagen fiber alignment and immune evasion. PAR-CLIP confirmed VIRMA binding to TFAP2A mRNA and RIP confirmed HNRNPC recognition. |
PAR-CLIP, RIP, Me-RIP, ChIP, dual-luciferase, in vivo mouse model |
Molecular medicine |
Medium |
37528369
|
| 2023 |
KIAA1429 stabilizes RAB27B mRNA through the m6A/YTHDF1 axis in CML cells, promoting proliferation and drug efflux (imatinib resistance). Rucaparib was found to suppress KIAA1429 expression. |
siRNA knockdown, RIP, m6A quantification, RNA stability assay, in vivo xenograft |
Genes & diseases |
Medium |
37692484
|
| 2023 |
KIAA1429 mediates m6A modification of PTGS2 mRNA, enhancing PTGS2 mRNA stability in nasopharyngeal carcinoma cells. |
MeRIP, mRNA stability assay, siRNA/overexpression, rescue experiment |
Critical reviews in immunology |
Low |
37830191
|
| 2023 |
KIAA1429 promotes HCC cell ferroptosis resistance through m6A-dependent post-transcriptional modification of SLC7A11 (cystine/glutamate antiporter), as confirmed by RNA immunoprecipitation of KIAA1429 binding to m6A on SLC7A11 transcript and rescue with SLC7A11 overexpression. |
RIP, m6A inhibitor (cycloleucine), subcutaneous xenograft, ferroptosis markers |
Journal of cellular and molecular medicine |
Medium |
37830241
|
| 2023 |
KIAA1429 mediates m6A modification of HOXA1 mRNA at its 3'UTR, enhancing HOXA1 mRNA stability and promoting gefitinib resistance in NSCLC. |
shRNA knockdown, in vivo xenograft, RNA stability assay targeting 3'-UTR |
Cell death discovery |
Low |
34001850
|
| 2024 |
PTPRG physically interacts with VIRMA in mouse brains and upregulates VIRMA m6A methyltransferase activity, which inhibits translation of PRKN mRNA, suppressing mitophagy and leading to neuronal death in Alzheimer's disease models. |
Single-cell RNA-seq, spatial transcriptomics, Co-IP of PTPRG-VIRMA in mouse brain, 5×FAD mouse validation |
Pharmacological research |
Medium |
38325728
|
| 2024 |
BRAF-mediated phosphorylation of KIAA1429 promotes its accumulation in the cytoplasm, where cytoplasmic KIAA1429 promotes Wnt pathway activation by binding and stabilizing FZD7, enhancing cancer stemness and oxaliplatin resistance in BRAF-mutated CRC. Nuclear-cytoplasmic distribution of KIAA1429 is regulated by BRAF phosphorylation. |
IP-MS, Co-IP, immunofluorescence, RIP, RNA-seq, in vitro/in vivo OXA-resistance models |
Journal of experimental & clinical cancer research : CR |
High |
40611274
|
| 2024 |
TIP60 acetylates KIAA1429 at a specific site, promoting KDM5B expression in an m6A-YTHDF1-dependent manner, which then suppresses FoxO1 transcription and facilitates HCC immune evasion via PD-L1 upregulation. RNA pulldown, RIP, ChIP, and Co-IP validated these interactions. |
RNA pulldown, RIP, ChIP, Co-IP, m6A dot blot, MeRIP-qPCR, flow cytometry, in vivo NOD/SCID model |
Cell death discovery |
Medium |
40301310
|
| 2024 |
CAF-derived EV-packaged circTAX1BP1 binds to VIRMA and promotes its lactylation at lysine residue 1713 by recruiting AARS2, thereby enhancing m6A-based modification and stability of SP1 mRNA and promoting colorectal liver metastasis. |
Co-IP, mass spectrometry, site-specific lactylation identification, MeRIP, RNA stability assay, in vivo PDX model |
Advanced science |
High |
41017455
|
| 2024 |
KIAA1429 promotes osteoclast differentiation inhibition and protects against osteoporosis by mediating m6A modification of Lrp4 mRNA; YTHDC1 reads the m6A mark to increase Lrp4 stability and expression, with LRP4 then recruiting TNFAIP3 to inactivate NF-κB signaling. |
scRNA-seq, RNA-seq, MeRIP-qPCR, RIP, in vitro osteoclast assays, OVX mouse model |
Cellular & molecular biology letters |
Medium |
41146006
|
| 2024 |
KIAA1429 cooperates with the m6A reader HuR to enhance HK1 mRNA stability in liver cancer, promoting the Warburg effect; KIAA1429 directly binds HK1 mRNA via m6A modification sites as shown by MeRIP-seq and RIP-seq. |
RNA-seq, MeRIP-seq, RIP, RNA stability assay, in vivo xenograft |
Biochemical pharmacology |
Medium |
38996929
|
| 2024 |
EET-induced N6-methyladenosine methylation of the transcription factor MAF via the DNA-CCDC25-VIRMA pathway enhances MAF mRNA stability and promotes Tfh cell differentiation in bullous pemphigoid. |
RNA sequencing, MeRIP, RNA stability assay, Co-IP, neutralizing antibody experiments, in vivo BP mouse model |
The Journal of allergy and clinical immunology |
Medium |
39490750
|
| 2024 |
VIRMA promotes glycolysis and tumor progression in pancreatic ductal adenocarcinoma by m6A-dependent upregulation of STRA6 mRNA via 3'UTR targeting; IGF2BP2 critically contributes to STRA6 mRNA stability, and the STRA6/STAT3 axis increases HIF-1α levels. |
RNA-seq, m6A-seq, RIP, RNA stability assay, in vivo and in vitro functional assays |
Cancer letters |
Medium |
38604311
|
| 2025 |
VIRMA-mediated m6A modification is essential for ribosome biogenesis in neural progenitor/stem cells during forebrain development. VIRMA depletion destabilizes the entire writer complex, reduces m6A levels, impairs ribosome biogenesis by inhibiting mRNA decay, triggers p53-dependent stress response, and compromises global protein synthesis, causing forebrain developmental defects. |
Conditional KO, ribosome profiling, RNA stability assay, proteomic analysis, in vivo brain development phenotype |
Science advances |
High |
40577453
|
| 2025 |
FEZF1-AS1 lncRNA binds to IGF2BP3, which enhances KIAA1429 mRNA stability and expression; KIAA1429 then facilitates m6A modification on OTUB1 mRNA, promoting OTUB1 expression through YTHDF1; OTUB1 stabilizes SLC7A11 by deubiquitination, suppressing ferroptosis in multiple myeloma. |
RNA pulldown, RIP, Co-IP, ubiquitination assay, m6A quantification, MeRIP, RNA stability assay |
Human cell |
Medium |
41085851
|
| 2025 |
IL-6 activates KIAA1429 expression through the JAK1/STAT3 pathway in endometrial cancer; KIAA1429 then installs m6A modification on DDIT3 mRNA, promoting its degradation and inhibiting ferroptosis, as validated by RIP, m6A stability assay, and FISH. |
RIP, RNA stability assay, FISH, dot blot, MeRIP, in vivo xenograft |
Cellular signalling |
Medium |
40436288
|
| 2025 |
Alcohol increases C/EBPβ expression, which binds to VIRMA's promoter and enhances its transcription; VIRMA then facilitates SLC43A2 mRNA degradation through an m6A-YTHDF2 pathway, reducing phenylalanine absorption and oxidative stress to drive PDAC progression. |
ChIP, MeRIP, RNA stability assay, RIP, in vitro/in vivo functional assays |
Oncogene |
Medium |
39900725
|
| 2026 |
VIRMA-mediated m6A modification and IGF2BP3-dependent interaction collectively maintain ANLN mRNA stability in intrahepatic cholangiocarcinoma; ANLN activates RhoA signaling, which inhibits the Hippo pathway, forming a YAP1-TEAD1-ANLN positive feedback loop promoting ICC growth. |
MeRIP, RIP, RNA stability assay, bioinformatic analysis, in vitro/in vivo ICC models, clinical cohort validation |
Cell death & disease |
Medium |
41513610
|
| 2025 |
KIAA1429 directly binds the 3'UTR of MYC mRNA and catalyzes site-specific m6A methylation, enhancing MYC mRNA stability and protein expression in clear cell renal cell carcinoma. |
Functional assays, in vivo xenograft, RIP, m6A site mapping at 3'UTR |
iScience |
Medium |
41907423
|