| 2004 |
PRMT7 is a protein arginine methyltransferase that catalyzes S-adenosylmethionine-dependent monomethylation of arginine residues in peptides containing RGG motifs; both putative AdoMet-binding domains (arising from gene duplication) are required for activity, as truncated single-domain proteins are enzymatically inactive. |
In vitro methylation assay with GST-PRMT7 fusion protein, HPLC purification, cation-exchange chromatography of hydrolysis products; domain truncation mutagenesis |
The Journal of biological chemistry |
High |
15044439
|
| 2004 |
PRMT7 expressed in E. coli and mammalian cells methylates histones, myelin basic protein, fibrillarin GAR fragment, and SmB, producing predominantly monomethylarginine and symmetric dimethylarginine (SDMA); a GRG tripeptide motif is sufficient for symmetric dimethylation. |
Immunopurified PRMT7, in vitro methylation assay, amino acid analysis |
The Journal of biological chemistry |
Medium |
15494416
|
| 2006 |
PRMT7 interacts with CTCFL/BORIS and is expressed in embryonic testis coinciding with H19 ICR methylation timing; CTCFL stimulates PRMT7 histone methyltransferase activity through interactions with both histones and PRMT7; H4R3me2s (symmetric) accumulates at H19 ICR and Gtl2 DMR chromatin in testis; co-injection of CTCFL, PRMT7, and Dnmt3a/b/L in Xenopus oocytes establishes H19 ICR methylation. |
Co-immunoprecipitation, ChIP, in vitro histone methyltransferase assay, Xenopus oocyte nuclear injection |
PLoS biology |
High |
17048991
|
| 2012 |
Human PRMT7 is a type III enzyme that exclusively produces ω-NG-monomethylarginine under all tested conditions; it does not produce asymmetric or symmetric dimethylarginine on peptides, GST-GAR, myelin basic protein, or histones H2A–H4. |
In vitro methylation assay with GST-PRMT7, multiple substrates and conditions; comparison with PRMT1 and PRMT5 controls |
The Journal of biological chemistry |
High |
22241471
|
| 2013 |
Mouse PRMT7 expressed in insect cells is a type III monomethylarginine-only enzyme; histone H2B is a highly preferred substrate; PRMT7 preferentially methylates arginine residues within RXR motifs surrounded by basic residues; Asp-147 and Glu-149 in the double E loop modulate substrate preference, and Glu-478 mutation nearly abolishes activity. |
Recombinant protein purification, in vitro methylation assay with multiple substrates, site-directed mutagenesis, mass spectrometry identification of methylation sites |
The Journal of biological chemistry |
High |
24247247
|
| 2014 |
PRMT7 promotes EMT and metastasis in breast cancer by binding to the E-cadherin proximal promoter and elevating H4R3me2s and reducing H3K4me3 and histone acetylation; PRMT7 interacts with YY1 and HDAC3 and recruits them to the E-cadherin promoter to repress its expression. |
ChIP, Co-IP, siRNA knockdown, cell migration/invasion assays |
Cancer research |
Medium |
25136067
|
| 2014 |
Acidic residues Asp-147 and Glu-149 in the double E loop of PRMT7 modulate substrate preference, and Glu-478 in the C-terminal domain is essential for catalytic activity; PRMT7 shows unusual temperature dependence with optimum well below 37°C. |
Site-directed mutagenesis, in vitro methylation assay with GST-PRMT7 fusion |
The Journal of biological chemistry |
High |
25294873
|
| 2015 |
PRMT7 and PRMT5 share a cofactor-binding site; DS-437, designed using PRMT5 structural information, inhibits both PRMT5 (IC50 6 µM) and PRMT7 with the same potency, acting as a cofactor competitor, suggesting a common SAM-binding scaffold. |
Biochemical inhibition assay, selectivity panel against 29 methyltransferases, cellular SDMA inhibition assay |
ACS medicinal chemistry letters |
Medium |
25893041
|
| 2015 |
PRMT7 represses the miR-24-2 gene in mouse ESCs by increasing H4R3me2s levels at its locus; depletion of PRMT7 reduces H4R3me2s, de-represses miR-24-3p and miR-24-2-5p, which in turn suppress Oct4, Nanog, Klf4, and c-Myc to promote differentiation. |
ChIP, reporter assays, RNA-seq, PRMT7 depletion and anti-miRNA rescue in mouse ESCs |
Nucleic acids research |
Medium |
27625395
|
| 2015 |
In B cells, PRMT7 recruits H4R3me1 and symmetric H4R3me2 to the Bcl6 promoter, negatively regulating Bcl6 expression; B cell-specific PRMT7 knockout mice show decreased marginal zone B cells, promoted germinal center formation, and altered Bcl6, Prdm1, and Irf4 expression. |
Conditional knockout mice, ChIP-PCR, overexpression in lymphoma cell lines |
Journal of immunology |
Medium |
26179907
|
| 2016 |
PRMT7 deficiency in satellite cells causes cell-cycle arrest and premature cellular senescence with elevated p21CIP1 and decreased DNMT3b; restoration of DNMT3b in PRMT7-deficient cells rescues senescence, placing PRMT7 upstream of DNMT3b/p21 axis in muscle stem cell self-renewal. |
Conditional knockout (Pax7-CreERT2), muscle injury/regeneration assays, epistasis by DNMT3b rescue |
Cell reports |
High |
26854227
|
| 2016 |
PRMT7 regulates skeletal muscle oxidative metabolism by interacting with and activating p38MAPK, which in turn activates ATF2 to transcriptionally upregulate PGC-1α; Prmt7-/- muscles show reduced oxidative metabolism, PGC-1α expression, and exercise capacity. |
Prmt7 knockout mice, Co-IP, reporter assays, siRNA depletion in myoblasts |
Diabetes |
Medium |
27207521
|
| 2016 |
PRMT7 loss-of-function in humans (homozygous deletion of transcription start site) causes decreased protein arginine methylation of histones H2B and H4, and the resulting patient cells show altered Wnt signaling. |
Patient-derived cells, methylation assays, Wnt pathway reporter |
Clinical genetics |
Medium |
27718516
|
| 2017 |
PRMT7 directly interacts with argininosuccinate synthetase 1 (ASS1) via pull-down; citrullinemia type I mutations in ASS1 disrupt this interaction; evolutionary co-analysis supports co-evolution of interacting residues. |
Yeast two-hybrid screen, pull-down assay, site-directed mutagenesis, computational interface mapping |
Journal of molecular biology |
Medium |
28587924
|
| 2018 |
PRMT7 promotes epiboly and gastrulation cell movements in zebrafish by facilitating syntenin; PRMT7 regulates F-actin organization in the enveloping layer and yolk syncytial layer; rescue experiments with either Prmt7 or syntenin re-expression restore normal epiboly. |
Morpholino knockdown in zebrafish, rescue by mRNA injection, F-actin staining |
Acta biochimica et biophysica Sinica |
Medium |
30383201
|
| 2019 |
PRMT7 methylates p38MAPKα at arginine residue 70, promoting its activation, which enhances MyoD activities; the R70A mutation in p38MAPKα impedes MyoD/E47 heterodimerization and recruitment of Prmt7, MyoD, and Baf60c to the Myogenin promoter, blunting Myogenin expression. |
In vitro methylation assay identifying R70, site-directed mutagenesis (R70A), ChIP, Co-IP, differentiation assays |
Cell death and differentiation |
High |
31243342
|
| 2019 |
PRMT7 promotes Sonic Hedgehog signaling by methylating GLI2 at arginine residues 225 and 227 near its SUFU-binding region; this methylation reduces GLI2-SUFU interaction, leading to increased GLI2 nuclear accumulation and Shh target gene activation, suppressing cellular senescence. |
Co-IP, in vitro methylation assay, site-directed mutagenesis, GLI2 reporter assay, PRMT7 KO MEFs |
Cell death and differentiation |
High |
31000813
|
| 2019 |
PRMT7 interacts with and methylates eIF2α in vitro and in breast cancer cells; PRMT7-mediated arginine methylation of eIF2α regulates its phosphorylation status at serine 51; PRMT7 is required for eIF2α-dependent stress granule formation under various cellular stresses. |
Quantitative MS interactome, in vitro methylation assay, stress granule imaging, siRNA knockdown |
Molecular biology of the cell |
Medium |
30699057
|
| 2019 |
PRMT7 interacts with and methylates C/EBP-β upon adipogenic induction; PRMT7 depletion increases adipogenesis and promotes mitotic clonal expansion; PRMT7 modulates C/EBP-β accumulation at PPAR-γ2 promoter target sites. |
Co-IP, ChIP, PRMT7 KO MEFs, adipogenesis assays |
Biochemical and biophysical research communications |
Medium |
31371025
|
| 2020 |
PRMT7 drives methylation of HSP70 at R469 in vitro; this methylation requires an ATP-bound, open conformation of HSP70; pharmacological inhibition or knockout of PRMT7 drastically reduces arginine monomethylation of HSP70 family proteins and decreases cellular tolerance to heat shock and proteasome inhibitors. |
Crystal structure/structural analysis, in vitro methylation assay with conformation-specific HSP70, PRMT7 inhibitor (SGC3027/SGC8158), PRMT7 KO cells |
Nature communications |
High |
32409666
|
| 2020 |
PRMT7 methylates SHANK2 at R240, causing di-methylation that disrupts the SPN-ANK domain blockade of SHANK2 and promotes co-accumulation of dynamin2, talin, FAK, and cortactin on endosomes, activating endosomal FAK/cortactin signaling to promote breast cancer metastasis. |
In vitro methylation assay, site-directed mutagenesis (R240), endosomal fractionation, Co-IP, cell migration/invasion assays, xenograft model |
eLife |
High |
32844749
|
| 2020 |
PRMT7 upregulates C-MYC expression in renal cell carcinoma by methylating β-catenin, inhibiting its ubiquitin-mediated degradation and thereby activating β-catenin/C-MYC signaling to promote cell proliferation. |
Co-IP, ubiquitination assay, siRNA/overexpression, methyltransferase inhibitor (Adox), xenograft model |
The international journal of biochemistry & cell biology |
Medium |
31926310
|
| 2021 |
PRMT7 forms aggregates to catalyze MAVS monomethylation at R52, attenuating MAVS binding to TRIM31 and RIG-I and suppressing MAVS aggregation and antiviral signaling; upon viral infection, PRMT7 undergoes automethylation at R32, SMURF1 is recruited to PRMT7 by MAVS, and PRMT7 is targeted for proteasomal degradation, relieving suppression of antiviral defense. |
In vitro methylation assay, site-directed mutagenesis, Co-IP, PRMT7 KO cells and mice, viral infection assays |
Molecular cell |
High |
34171297
|
| 2021 |
PRMT7 catalyzes H4R3me1 at the Foxm1 gene promoter to activate Foxm1 transcription, regulating cell cycle genes and thereby controlling alveolar myofibroblast proliferation and differentiation during lung alveologenesis. |
ChIP, PRMT7 KO mice, Foxm1 overexpression rescue, myofibroblast isolation |
Cell death & disease |
Medium |
34497269
|
| 2022 |
In COPD, NF-κB/RelA activation in monocytes induces PRMT7 transcription, which leads to H4R3me1 at the RAP1A gene locus, increasing RAP1A transcription and promoting monocyte adhesion and migration; persistent monocyte-derived macrophage accumulation causes ALOX5/LTB4 overproduction and ACSL4-mediated ferroptosis in lung epithelial cells. |
Conditional PRMT7 KO mice, ChIP, NF-κB pathway analysis, COPD patient tissue analysis, lung fibrosis and skin injury models |
Nature communications |
High |
35288557
|
| 2022 |
Loss of PRMT7 in CML reduces expression of glycine decarboxylase, reprogramming glycine metabolism to generate methylglyoxal, which is detrimental specifically to leukemia stem cells; genetic Prmt7 deletion or pharmacological PRMT7 inhibition selectively impairs CML LSC self-renewal without affecting normal hematopoiesis. |
Prmt7 genetic KO in CML mouse model, specific PRMT7 inhibitor, primary CML CD34+ cells, metabolomics |
Cell metabolism |
High |
35508169
|
| 2022 |
PRMT7 deficiency in B16.F10 melanoma reduces DNMT expression and causes loss of DNA methylation at endogenous retroviral element (ERV) regulatory regions, increasing ERV expression and activating dsRNA sensing by RIG-I and MDA5; H4R3me2s is reduced at RIG-I and MDA5 promoters in PRMT7-deficient cells. |
PRMT7 KO and inhibitor (SGC3027), bisulfite sequencing, ChIP, RNA-seq, in vivo tumor growth with immune checkpoint blockade |
Cell reports |
Medium |
35354055
|
| 2022 |
PRMT7 deficiency in cardiomyocytes decreases symmetric dimethylation of β-catenin at arginine 93, resulting in enhanced β-catenin activity and Wnt signaling, leading to cardiac hypertrophy and fibrosis. |
Cardiomyocyte-specific PRMT7 KO mice, in vitro methylation assay identifying R93 on β-catenin, β-catenin activity assays, cardiac transcriptome analysis |
Cellular and molecular life sciences |
Medium |
35089423
|
| 2022 |
PRMT7-mediated histone arginine monomethylation regulates RUNX1 target gene expression in T-ALL; CRISPR deletion of PRMT7 changes arginine monomethylation patterns in protein complexes associated with RNA/DNA processing including RUNX1. |
CRISPR-Cas9 KO, proteomic arginine methylation profiling, colony formation assay |
Cancers |
Medium |
35565298
|
| 2023 |
PRMT7 methylates PTEN, promoting its arginine methylation; PRMT7 enhances PTEN transcription by increasing H3R2me1 at the PTEN promoter; PRMT7 interacts with PTEN protein and stabilizes nuclear PTEN; PRMT7 inhibits PI3K/AKT signaling in gastric cancer through PTEN regulation. |
Co-IP, ChIP, in vitro methylation, PRMT7 overexpression/knockdown, PI3K/AKT signaling readouts |
Journal of Cancer |
Medium |
37781082
|
| 2024 |
PRMT7 methylates MAVS at arginine R232 (R232me1), reducing MAVS/RIG-I interaction and MAVS aggregation; RNA virus infection downregulates PRMT7 and decreases R232me1, enhancing MAVS/RIG-I interaction and antiviral signaling; knock-in mice with MAVS R232K substitution are more resistant to VSV infection; a peptide inhibitor of PRMT7-MAVS interaction (PiPRMT7-MAVS) suppresses R232me1 and enhances antiviral immunity. |
In vitro methylation assay, MAVS R232K knock-in mice, VSV infection, Co-IP, peptide inhibitor design |
Proceedings of the National Academy of Sciences of the United States of America |
High |
39546576
|
| 2024 |
PRMT7 activates HLH-30/TFEB nuclear transactivation in C. elegans by methylating HLH-30 on its RAG complex binding domain, facilitating nuclear localization; this function is evolutionarily conserved in human TFEB and intestinal cells responding to bacterial pore-forming toxins. |
C. elegans genetics (prmt-7 mutants), in vitro methylation, TFEB localization assays in human intestinal cells |
Autophagy |
Medium |
38261662
|
| 2024 |
PRMT7 catalyzes H4R3me1 at the HMGB2 promoter to activate HMGB2 transcription; HMGB2 then facilitates ACSL1 transcription, promoting ferroptosis; inhibition of PRMT7 suppresses the HMGB2-ACSL1 ferroptosis pathway in pancreatitis. |
ChIP, overexpression/KO, ferroptosis assays, PRMT7 inhibitor in SAP model |
Journal of proteome research |
Medium |
38376246
|
| 2024 |
AKT1 phosphorylates PRMT7 at threonine 73 (T73), promoting PRMT7 activity; phosphorylated PRMT7 monomethylates GLUD1 at R76, stabilizing GLUD1 by antagonizing ubiquitin-dependent degradation, thereby enhancing glutamine metabolism and gastric cancer progression. |
In vitro phosphorylation and methylation assays, site-directed mutagenesis, Co-IP, ubiquitination assay, xenograft model |
Cell death & disease |
Medium |
41876450
|
| 2024 |
PRMT7 promotes osteogenic differentiation of mesenchymal stem cells by increasing H3R2me1 levels at the PTEN promoter to enhance PTEN transcription; PRMT7 also interacts with PTEN protein and stabilizes nuclear PTEN by preventing its ubiquitination and degradation; female-specific conditional Prmt7 KO impairs osteogenesis, rescued by PTEN overexpression. |
Conditional KO mice (female-specific phenotype), ChIP, Co-IP, ubiquitination assay, PTEN rescue experiments |
International journal of molecular sciences |
Medium |
40243588
|
| 2024 |
PRMT7 methylates Fhod1 and Fhod3 (formin homology domain proteins) at arginine residues in the diaphanous autoinhibitory domain (DAD), specifically R1588 and/or R1590 of Fhod3 isoform 4; prior phosphorylation of S1589 by ROCK1 prevents subsequent PRMT7 methylation of R1588/R1590, revealing phosphorylation-methylation crosstalk on the DAD domain. |
In vitro methylation assay, in vitro ROCK1 phosphorylation assay, site-directed mutagenesis, sequential PTM competition assay |
The Journal of biological chemistry |
High |
39368550
|
| 2024 |
PRMT7 controls JAK/STAT signaling in cardiomyocytes by regulating expression of SOCS3, a negative feedback inhibitor of JAK/STAT; Prmt7 cardiac KO leads to dysregulated JAK/STAT signaling; 17β-estradiol attenuates doxorubicin-induced decreases in PRMT7 expression, and PRMT7 depletion abrogates estrogen's cardioprotective effect. |
Cardiac-specific KO mice, transcriptome analysis, cardiomyocyte-specific siRNA, E2 treatment |
Experimental & molecular medicine |
Medium |
38486105
|
| 2023 |
PRMT7 substrate recognition of RXR motifs is primarily determined by differences in Vmax rather than apparent Km; even subtle substitutions (e.g., K30R and R31K) in the RXR context of histone H2B greatly reduce methylation; ionic strength reduces PRMT7 activity mainly by increasing apparent Km. |
In vitro methylation kinetics with synthetic peptides and full-length histones, Xenopus laevis H2B substitution variants |
PloS one |
Medium |
37216364
|
| 2019 |
In Leishmania, PRMT7 is a cytoplasmic protein that methylates RNA-binding proteins Alba3 and RBP16; PRMT7-dependent methylation promotes Alba3 association with specific target transcripts including δ-amastin mRNA, thereby stabilizing this virulence factor transcript; PRMT7 KO reduces RNA-binding capacity of Alba3 and affects RBP16 protein stability. |
Comparative methyl-SILAC proteomics, in vitro methylation assay, RNA immunoprecipitation, PRMT7 KO in Leishmania |
Nucleic acids research |
Medium |
32365184
|