| 2017 |
TRIM29 induces K48-linked ubiquitination of STING (Stimulator of Interferon Genes), leading to its rapid proteasomal degradation, thereby suppressing the cytosolic dsDNA-sensing innate immune pathway and promoting DNA virus persistence. |
Mechanistic studies in human airway epithelial cells and Trim29-/- mice; ubiquitination assays; knockdown and knockout functional readouts (IFN production, viral titers) |
Nature communications |
High |
29038422
|
| 2018 |
TRIM29 targets STING for K48-linked ubiquitination and proteasomal degradation in macrophages and dendritic cells, negatively regulating the STING-TBK1-IRF3 signaling axis in response to DNA viruses and cytosolic dsDNA. |
Ubiquitination assays, TRIM29 KO mice (HSV-1 infection model), IFN measurement, Western blot for STING degradation |
Cell discovery |
High |
29581886
|
| 2016 |
TRIM29 directly binds NEMO (IKK-γ) and induces its K48-linked ubiquitination and proteasomal degradation, thereby inhibiting both IRF- and NF-κB-mediated signaling in alveolar macrophages. |
Co-immunoprecipitation, ubiquitination assay, Trim29-/- mouse model (influenza and H. influenzae challenge), cytokine measurement |
Nature immunology |
High |
27695001
|
| 2018 |
TRIM29 interacts with MAVS and induces its K11-linked ubiquitination and proteasomal degradation, negatively regulating type I IFN production in response to dsRNA viruses (reovirus, poly I:C). |
Co-immunoprecipitation, ubiquitination assay, Trim29-/- mouse model (reovirus challenge), IFN measurement |
Journal of immunology |
High |
29769269
|
| 2010 |
ATDC/TRIM29 binds p53, sequesters it outside the nucleus, and represses p53-regulated gene expression (p21, NOXA), thereby promoting cell proliferation and resistance to ionizing radiation. This interaction is modulated by acetylation of lysine 116 on ATDC. |
Co-immunoprecipitation, reporter gene assays, immunofluorescence (p53 localization), RNAi silencing, cell proliferation assays |
Molecular and cellular biology |
High |
20368352
|
| 2010 |
HDAC9 co-purifies with TRIM29/ATDC and deacetylates it, thereby altering TRIM29's ability to associate with p53 and inhibiting TRIM29's cell proliferation-promoting activity. |
Biochemical co-purification, deacetylation assay, co-immunoprecipitation, cell proliferation assays |
The Journal of biological chemistry |
High |
20947501
|
| 2011 |
TRIM29 binds Tip60 acetyltransferase (identified by yeast two-hybrid screening), promotes Tip60 degradation and altered localization, and reduces Tip60-mediated acetylation of p53 at lysine 120, thereby suppressing apoptosis and enhancing cell growth. |
Yeast two-hybrid, co-immunoprecipitation, Western blot for Tip60 levels, p53-K120 acetylation assay, UV-induced apoptosis assay (HCT116 cells) |
Biochimica et biophysica acta |
Medium |
21463657
|
| 2015 |
TRIM29 functions as a histone-binding scaffold protein that interacts with BRCA1-associated surveillance complex, cohesin, DNA-PKcs, and components of the TIP60 complex, assembling them into damaged chromatin; TRIM29 binding to modified H3 and H4 tails in nucleosomes is required for H2AX phosphorylation and cell viability after ionizing radiation. |
Mass spectrometry-based proteomics (MudPIT), co-immunoprecipitation, histone binding assays, chromatin fractionation, γH2AX readout, clonogenic survival after IR |
Nature communications |
High |
26095369
|
| 2014 |
ATDC/TRIM29 is directly phosphorylated by MAPKAP kinase 2 (MK2) at Serine 550 in an ATM-dependent manner, and this phosphorylation is required for ATDC's radioprotective function in pancreatic cancer cells. |
In vitro kinase assay (MK2 phosphorylating ATDC), site-directed mutagenesis (S550 mutants), clonogenic survival after IR, mouse xenograft model |
Cancer research |
High |
24469230
|
| 2014 |
ATDC/TRIM29 overexpression in vivo drives both noninvasive and invasive bladder carcinoma in transgenic mice by suppressing miR-29 expression, leading to DNMT3A upregulation, DNA methylation, and silencing of the tumor suppressor PTEN. |
Transgenic mouse model (ATDC overexpression), miRNA profiling, DNMT3A and PTEN expression analysis, methylation assays |
Cancer research |
High |
26471361
|
| 2014 |
TRIM29 suppresses invasive breast cancer behavior by inhibiting TWIST1 activity; TWIST1 transcriptionally represses TRIM29 expression by directly binding E-box elements in the TRIM29 promoter, establishing a negative regulatory feedback loop. |
RNAi silencing, TWIST1 overexpression/knockdown, promoter-luciferase reporter assay with E-box mutation, EMT marker analysis (E/N-cadherin, vimentin, EpCAM) |
Cancer research |
Medium |
24950909
|
| 2019 |
TRIM29 ubiquitinates and degrades TAB2 (TGF-β-activated kinase 1 binding protein 2) in NK cells following activation, thereby negatively regulating IFN-γ production; TRIM29-deficient NK cells produce more IFN-γ and protect mice from murine CMV infection. |
Co-immunoprecipitation, ubiquitination assay, TRIM29-specific NK cell knockout mice (CMV challenge), IFN-γ measurement |
Journal of immunology |
High |
31270148
|
| 2018 |
Loss of TRIM29 in squamous cell carcinoma cells leads to ectopic keratin localization; TRIM29 interacts with keratins and keratin-interacting protein FAM83H to regulate the keratin distribution network. |
Comprehensive proteomics, co-immunoprecipitation, immunofluorescence (keratin localization), TRIM29 knockdown/overexpression migration/invasion assays |
Cancer research |
High |
30389700
|
| 2019 |
TRIM29 interacts with IGF2BP1 and induces its K48-linked ubiquitination at Lys440 and Lys450, leading to IGF2BP1 degradation; loss of IGF2BP1 reduces PD-L1 mRNA stability, enhancing anti-tumor T-cell immunity in gastric cancer. |
Proteomics, co-immunoprecipitation, in vitro ubiquitination assay (specific lysine sites), PD-L1 3'UTR reporter assay, in vivo tumor model |
Cancer letters |
High |
38029830
|
| 2024 |
TRIM29 interacts with PERK (protein kinase RNA-like ER kinase) and promotes SUMOylation of PERK to maintain its stability, thereby sustaining PERK-mediated ER stress, apoptosis, and ROS responses that promote viral replication in cardiomyocytes during viral myocarditis. |
Co-immunoprecipitation, SUMOylation assay, TRIM29-/- mouse model (cardiotropic virus challenge), PERK inhibitor (GSK2656157) in vivo treatment, cardiac function readouts |
Nature communications |
High |
38664417
|
| 2024 |
TRIM29 promotes K48-linked ubiquitination and degradation of both NLRP6 and NLRP9b in intestinal epithelial cells, suppressing IFN-λ and IL-18 production during enteric RNA virus infection, thereby facilitating viral-induced intestinal inflammation. |
TRIM29 knockout in intestinal epithelial cells (rotavirus and EMCV models), ubiquitination assay, cytokine measurement (IFN-λ, IL-18), immune cell recruitment analysis |
Mucosal immunology |
High |
39396665
|
| 2019 |
TRIM29 knockdown in pancreatic cancer cells destabilizes ISG15 protein by promoting its processing via calpain 3 (CAPN3); TRIM29 normally protects ISG15 from CAPN3-mediated cleavage, and extracellular free ISG15 (secreted) maintains cancer stem cell-like features via autocrine signaling. |
TRIM29 knockdown, CAPN3 inhibitor treatment, ISG15 stability assays, stem cell sphere formation, rescue experiments with secreted ISG15 |
Oncogene |
Medium |
31501523
|
| 2021 |
TRIM29 directly binds YAP1 and reduces its K48-linked ubiquitination and degradation, thereby stabilizing YAP1 and promoting pancreatic cancer cell proliferation. |
Co-immunoprecipitation, in vitro ubiquitination assay, YAP1 protein stability analysis, rescue proliferation experiments, mouse xenograft |
Journal of translational medicine |
Medium |
34353343
|
| 2021 |
TRIM29 promotes degradation of pyruvate kinase M1 (PKM1) via the ubiquitin-proteasome pathway by directly targeting PKM1, reducing the PKM1/PKM2 ratio and promoting PKM2-mediated aerobic glycolysis (Warburg effect) in colorectal cancer. |
Co-immunoprecipitation, ubiquitination assay, PKM1/PKM2 ratio analysis, metabolic assays, TRIM29 knockdown/overexpression in vitro and in vivo |
Aging |
Medium |
33495406
|
| 2023 |
TRIM29 interacts with IκBα and mediates its K48-linked ubiquitination-dependent degradation, leading to NF-κB activation and downstream NLRP3 inflammasome-mediated podocyte pyroptosis in diabetic nephropathy. |
Co-immunoprecipitation, ubiquitination assay, TRIM29 overexpression/knockdown with NF-κB inhibitor rescue, NLRP3/caspase-1/GSDMD-N Western blot, flow cytometry for pyroptosis |
Cell biology international |
Medium |
36841942
|
| 2023 |
TRIM29 interacts with NLRC4 inflammasome protein and promotes its K48-linked polyubiquitination and proteasomal degradation in neurons and microglia, thereby reducing NLRC4 inflammasome activation and limiting neuronal injury in ischemic stroke. |
Co-immunoprecipitation with truncation mutants, ubiquitination assay, TRIM29 knockout mice (MCAO model), immunofluorescence for apoptosis/pyroptosis, cytokine measurement |
Stroke |
Medium |
37021569
|
| 2015 |
TRIM29 is required for regulation of the p63 (TAp63α)-mediated pathway in cervical cancer cells; TRIM29 controls TAp63α expression levels and modulates integrin expression and ZEB1 to regulate cell adhesion and invasion. |
TRIM29 knockdown and overexpression, TAp63α expression analysis, integrin profiling, cell adhesion and invasion assays |
Biochimica et biophysica acta |
Low |
26071105
|
| 2020 |
TRIM29 is required for efficient recruitment of 53BP1 to DNA double-strand break sites; TRIM29 knockout cells show impaired 53BP1 foci formation after etoposide, reduced NHEJ efficiency, and compensatory upregulation of RAD51-mediated homologous recombination. |
Gene targeting (homologous recombination) in DT40 cells, clonogenic survival assays, immunofluorescence for γH2AX, 53BP1, and RAD51 foci |
FEBS open bio |
Medium |
33017104
|
| 2025 |
USP18 interacts with TRIM29 and facilitates its K27-linked ubiquitination by recruiting TRIM21 (which directly ubiquitinates TRIM29 at Lys561); this promotes TRIM29 oligomerization and nuclear translocation, enhancing DNA damage response and radioresistance in nasopharyngeal carcinoma cells. |
Co-immunoprecipitation, ubiquitination assay (site-specific K561 mutant), immunofluorescence for nuclear translocation, radiosensitivity assays |
Cell death and differentiation |
Medium |
41219493
|
| 2023 |
TRIM29 interacts with VDAC1 to activate mitophagy, which clears damaged mitochondria and reduces ROS accumulation, thereby preventing cellular senescence in nasopharyngeal carcinoma cells. |
Co-immunoprecipitation, TRIM29 silencing with ROS measurement, mitophagy assays, cellular senescence assays, in vivo tumor growth |
Cancer science |
Medium |
37248790
|
| 2025 |
TRIM29 promotes K48-linked ubiquitination and proteasomal degradation of PRRSV nsp11 (binding via TRIM29's coiled-coil domain at conserved catalytic residue K173), thereby inhibiting nsp11's suppression of IFN-β and restricting PRRSV replication. |
Co-immunoprecipitation, in vitro ubiquitination assay (K173R mutant), domain-mapping experiments, IFN-β reporter assays, viral replication assays |
Journal of virology |
Medium |
41251350
|
| 2025 |
TRIM29 physically interacts with K14+ intermediate filaments in bladder cancer cells, and this interaction regulates focal adhesion stability (requiring ZYX) to drive cancer cell migration and invasion. |
Co-immunoprecipitation, KD/KO functional assays (migration, invasion), focal adhesion analysis, K14 and ZYX knockdown rescue experiments |
Oncogene |
Medium |
40908312
|
| 2024 |
O-GlcNAcylation of TRIM29 at threonine 120 (T120) is required for TRIM29-mediated adaptive responses of pancreatic cancer cells to glucose deficiency; TRIM29 and OGT form a feedback loop where OGT O-GlcNAcylates TRIM29, and TRIM29 promotes OGT translation. |
Western blot, mass spectrometry, WGA-immunoprecipitation, T120 site mutagenesis, protein stability and translation assays under glucose deprivation, crystal violet/flow cytometry functional assays |
Cellular oncology |
Medium |
38345749
|
| 2025 |
TRIM29 degrades YBX1 through K48-linked ubiquitination, thereby inhibiting the PI3K/AKT signaling pathway and reversing lenvatinib resistance in hepatocellular carcinoma. |
Co-immunoprecipitation, mass spectrometry, transcriptome sequencing, ubiquitination assay, colony formation/CCK8/flow cytometry, in vivo xenograft |
Translational oncology |
Medium |
39874728
|
| 2016 |
TRIM29 expression in breast tumor and non-tumorigenic mammary cells is negatively regulated by ATM: basal TRIM29 levels depend on NF-κB (RelA subunit) activity, and hypoxia-induced TRIM29 upregulation requires both ATM and HIF1α through increased TRIM29 gene transcription. |
ATM knockdown, RelA knockdown, HIF1α inhibition, hypoxia treatment, TRIM29 promoter-reporter assays, Western blot |
The Journal of biological chemistry |
Medium |
27535224
|
| 2021 |
TRIM29 maintains cancer stem cell-like features in ovarian cancer by facilitating SETBP1 transcriptional activation through the VEZF1 transcription factor; TRIM29 promotes VEZF1 mRNA translation by recruiting RNA-binding protein BICC1 to the VEZF1 3'UTR, and the SETBP1/SET/PP2A axis downstream mediates the CSC phenotype. |
Global proteomics, co-immunoprecipitation, RNA-immunoprecipitation (RIP), luciferase reporter, TRIM29 KD rescue experiments |
Cancer letters |
Medium |
34973391
|
| 2025 |
TRIM29 interacts with FAM83H, stabilizes it by reducing its ubiquitination and degradation, thereby redistributing cellular keratins, activating NF-κB, upregulating PLXNB2, and enhancing CRC cell adhesion and liver metastatic colonization. |
Multi-omics, co-immunoprecipitation, ubiquitination assay, FAM83H stability analysis, NF-κB and PLXNB2 pathway readouts, in vivo metastasis model |
Cellular signalling |
Medium |
40389046
|
| 2024 |
tRF-AspGTC binds galectin-3 and inhibits TRIM29-mediated ubiquitination of galectin-3, thereby stabilizing galectin-3, which activates TLR4/MyD88/NF-κB signaling to drive vascular smooth muscle cell phenotypic switching and intracranial aneurysm formation. |
Co-immunoprecipitation, ubiquitination assay, tRF-AspGTC gain/loss of function, galectin-3 stability assays, TLR4/NF-κB pathway readouts |
Research (Washington, D.C.) |
Medium |
39776588
|
| 2021 |
KLF4 binds a specific site in the TRIM29 promoter to transactivate its transcription, and KLF4-driven TRIM29 expression mediates KLF4-induced cell migration and modulation of the keratin network (keratin 8 phosphorylation at aa 432). |
Promoter-luciferase assay, ChIP or promoter binding assay, TRIM29 knockdown rescue of KLF4-induced migration, Western blot for KRT8 phosphorylation |
Biochemistry and biophysics reports |
Low |
34485714
|
| 2024 |
TRIM29 promotes PHLPP1 K48-linked ubiquitination and degradation in pancreatic ductal adenocarcinoma; TRIM29 is recruited by NAP1L5 which binds PHLPP1, and the resulting PHLPP1 degradation activates AKT/mTOR signaling. |
Co-immunoprecipitation, ubiquitination assay, PHLPP1 stability analysis, NAP1L5/TRIM29 knockdown, AKT/mTOR pathway readouts |
Biochemical pharmacology |
Medium |
37717692
|
| 2026 |
TRIM29 directly binds IκBα via its BB2 domain and catalyzes K48-linked ubiquitination and proteasomal degradation of IκBα, activating NF-κB signaling and promoting EMT in CXCL5+ pancreatic cancer cells to drive microvascular invasion. |
Co-immunoprecipitation (domain mapping), ubiquitination assay, ChIP-qPCR, migration/invasion assays, xenograft model |
Molecular cancer |
Medium |
41952208
|