| 2006 |
DRAM1 (DRAM) is a direct transcriptional target of p53 that encodes a lysosomal protein; p53 induces autophagy in a DRAM-dependent manner, and DRAM is essential for p53-mediated apoptosis. |
RNAi knockdown, overexpression, lysosomal localization by cell fractionation/imaging, p53-dependent induction assays |
Cell |
High |
16839881
|
| 2007 |
TA-p73 transcriptionally regulates DRAM but, unlike p53, p73's induction of autophagy is DRAM-independent; deltaN-p73 negatively regulates p53-induced and p73-induced autophagy but not starvation-induced autophagy. |
RNAi knockdown of DRAM, overexpression of p73 isoforms, autophagy flux assays |
Cell death and differentiation |
Medium |
17304243
|
| 2007 |
FLJ11259/DRAM1 is a direct p53 target gene with a functional p53 response element 22.3 kb upstream of the first coding exon; p53 binds this element in vivo (ChIP), and binding is enhanced after cisplatin treatment. The protein contains six transmembrane domains and localizes in a punctate cytoplasmic pattern. |
p53 siRNA knockdown, isogenic p53+/+ vs p53-suppressed cell lines, luciferase reporter assay, chromatin immunoprecipitation, GFP-fusion confocal microscopy |
Biochimica et biophysica acta |
High |
17397945
|
| 2009 |
DRAM1 is a lysosomal protein; a closely related paralogue DRAM2 (45% identity) also localizes to lysosomes but does not modulate autophagy on overexpression and is not induced by p53 or p73. Drosophila DmDRAM, the single fly orthologue, retains the ability to modulate autophagy. |
Overexpression with subcellular localization (immunofluorescence), autophagy flux assays, comparison of p53/p73 induction across paralogues |
Cell cycle (Georgetown, Tex.) |
Medium |
19556885
|
| 2009 |
JNK activation is required upstream of DRAM induction by 2-methoxyestradiol; JNK promotes DRAM expression in a p53-partially-regulated manner, and DRAM silencing reduces both autophagy and apoptosis triggered by 2-ME. |
siRNA knockdown of DRAM and JNK, pharmacological JNK inhibition, autophagy/apoptosis assays |
Cancer research |
Medium |
19706754
|
| 2012 |
DRAM1 promotes autophagy flux by enhancing lysosomal acidification (V-ATPase activity), promoting autophagosome-lysosome fusion, and activating lysosomal cathepsin D; siRNA knockdown of DRAM1 reduces lysosomal V-ATPase activity and slows clearance of autophagosomes. |
siRNA knockdown, RFP-LC3 flux assay, lysosomal pH measurement, cathepsin D activity assay, rapamycin washout experiment |
PloS one |
High |
23696801
|
| 2012 |
DRAM1 regulates p62 localization to autophagosomes and its autophagy-mediated degradation; DRAM1 knockdown decreases this process. DRAM1 and p62 cooperatively regulate cell motility and invasion in glioblastoma stem cells, associated with reduced ATP and lactate levels. Starvation- or mTOR/PI3K inhibition-induced autophagy is not affected by DRAM1 or p62 knockdown. |
siRNA knockdown, immunofluorescence localization of p62, invasion/migration assays, metabolic measurements |
Oncogene |
Medium |
22525272
|
| 2012 |
DRAM-1 encodes multiple p53-inducible splice variants (SV1, SV4, SV5); SV1 localizes to lysosomes/endosomes, SV4 partially localizes to peroxisomes and ER, SV5 partially localizes to autophagosomes and ER. SV4 and SV5 modulate autophagy without inducing programmed cell death. |
Cloning of splice variants, immunofluorescence co-localization with organelle markers, autophagy assays |
Autophagy |
Medium |
22082963
|
| 2013 |
DRAM1 interacts directly with BAX protein, inhibiting BAX degradation by autophagy, thereby increasing BAX protein levels in a transcription-independent manner. DRAM1 recruits BAX to lysosomes, triggering lysosomal cathepsin B release and BID cleavage, leading to mitochondrial cytochrome c release and caspase-3 activation. |
Co-immunoprecipitation, immunofluorescence, siRNA knockdown, BAX half-life measurement, cathepsin B/cytochrome c release assays |
Cell death & disease |
High |
25633293
|
| 2013 |
HIV infection induces DRAM expression in a p53-dependent manner in CD4+ T cells; DRAM knockdown inhibits autophagy and lysosomal membrane permeabilization (LMP), cytochrome C release, MOMP, and cell death, but increases viral production. |
siRNA knockdown of DRAM and p53, LMP assay, cytochrome C release, MOMP measurement, viral titer |
PLoS pathogens |
Medium |
23658518
|
| 2014 |
DRAM1 expression is induced downstream of the TLR/IL1R-MYD88-NF-κB innate immune sensing pathway in response to mycobacterial infection; DRAM1 activates selective autophagy against mycobacteria in a p53-independent manner requiring STING and p62/SQSTM1. |
MYD88/NF-κB inhibition, siRNA knockdown of DRAM1, overexpression, co-localization with Mtb, zebrafish and human macrophage infection models |
Cell host & microbe |
High |
24922577
|
| 2014 |
Phosphorylated AKT (p-AKT) binds DRAM in the cytoplasm, blocking DRAM translocation to mitochondria; inactivation of PI3K/AKT pathway rescues DRAM translocation to mitochondria, where DRAM induces mitophagy and apoptosis in hepatocellular carcinoma cells. |
Co-immunoprecipitation of p-AKT and DRAM, immunofluorescence tracking of DRAM localization, PI3K inhibition, siRNA knockdown |
Cell death & disease |
Medium |
24556693
|
| 2015 |
DRAM-3 (TMEM150B), a DRAM1-related protein, localizes to lysosomes/autolysosomes, endosomes, and plasma membrane; it modulates autophagy flux and promotes cell survival under glucose deprivation in an autophagy-independent manner. |
Immunofluorescence localization, CRISPR/Cas9 disruption, autophagy flux assays, clonogenic survival assay |
Cell death and differentiation |
Medium |
25929859
|
| 2018 |
Dram1 is required for genotoxic stress-induced alternative (Atg5-independent) autophagy; Dram1 functions in the closure of isolation membranes downstream of p53 in this alternative autophagy pathway. |
Dram1 overexpression/knockdown in cells with or without Atg5, electron microscopy of isolation membranes, epistasis with p53 |
Cell stress |
Medium |
31225467
|
| 2018 |
DRAM1 interacts with Atg7 (but not directly with Atg5 or Atg12), promoting formation of the Atg12-Atg5 conjugate; DRAM1 overexpression restores autophagic flux and autophagosome-to-autophagolysosome conversion in ischemic cardiomyocytes. Atg7 siRNA abolishes these effects. |
Co-immunoprecipitation (DRAM1 with Atg7, Atg5, Atg12), mRFP-GFP-LC3 flux assay, siRNA knockdown, adenoviral overexpression in rat AMI model |
Journal of molecular and cellular cardiology |
Medium |
30144448
|
| 2019 |
DRAM1 binds the membrane carrier protein SCAMP3 and amino acid transporters SLC1A5 and LAT1, directing them to lysosomes to permit efficient efflux of amino acids from lysosomes into the cytoplasm, which is required for mTORC1 activation. Loss of DRAM1 impairs mTORC1 activation, insulin signaling, glycemic balance, and adipocyte differentiation. This effect is autophagy-independent. |
Co-immunoprecipitation, lysosomal fractionation, amino acid efflux assays, DRAM-1 knockout mouse, mTORC1 activity measurements, adipocyte differentiation assay |
Molecular cell |
High |
31492633
|
| 2019 |
DRAM1 inhibits rpS6 phosphorylation in an mTORC1-dependent manner and inhibits activation of the PI3K-Akt pathway stimulated by growth factors; DRAM1 localizes at the plasma membrane and regulates phosphorylation of the IGF-1 receptor. |
FLAG-DRAM1 overexpression, siRNA knockdown, Western blot for phospho-rpS6/Akt/IGF-1R, immunostaining for DRAM1 localization, CCK-8 and colony formation assays |
Cell communication and signaling : CCS |
Medium |
30902093
|
| 2019 |
DRAM1 deficiency causes fragmentation of the Golgi apparatus; DRAM1 is partially localized in the Golgi, and its knockdown delays ER-to-plasma membrane transport of VSVG-GFP and impedes retrograde trafficking of CI-MPR from plasma membrane to Golgi. |
siRNA knockdown, immunofluorescence with Golgi markers, ts045-VSVG-GFP transport assay, CI-MPR trafficking assay |
Cellular signalling |
Medium |
31356858
|
| 2020 |
Dram1 deficiency in zebrafish reduces phagosome/vesicle acidification of Mycobacterium marinum-containing vesicles, impairs autophagic targeting of Mm, and leads to premature pyroptotic death of infected macrophages via caspase a/gasdermin Eb; knockdown of caspa and gsdmeb reverts the increased bacterial burden. |
Zebrafish dram1 CRISPR mutant, in vivo imaging of autophagic targeting, LysoTracker acidification assay, caspa/gsdmeb knockdown epistasis, RNA-seq |
Cell death & disease |
High |
32332700
|
| 2020 |
DRAM1 interacts with EPS15 to promote EGFR endocytosis, and recruits V-ATPase (V-ATP6V1 subunit) to lysosomes, increasing lysosomal V-ATPase assembly, lowering lysosomal pH, and activating lysosomal proteases, resulting in accelerated EGFR lysosomal degradation and suppression of EGFR signaling. |
Proximity labeling (BioID) followed by proteomics, co-IP of DRAM1 with EPS15, lysosomal pH measurement, EGFR degradation assay, xenograft tumor model |
Cell death & disease |
High |
32943616
|
| 2021 |
DRAM interacts with stomatin (STOM) and promotes its lysosomal localization; fatty acid-induced DRAM enhances lysosomal membrane permeabilization (LMP) and promotes exosome secretion from hepatocytes. DRAM knockout reverses high-fat diet-induced increase in exosome secretion. |
Co-immunoprecipitation of DRAM and STOM, DRAM knockout mouse model, siRNA knockdown, LMP assay, exosome quantification |
Science advances |
Medium |
34731006
|
| 2021 |
DRAM1 interacts with PKM2 and increases PKM2 levels at the plasma membrane; ethanol-induced DRAM1 in hepatocytes increases secretion of PKM2-enriched extracellular vesicles/ectosomes that promote macrophage M1 activation. |
Co-immunoprecipitation of DRAM1 and PKM2, DRAM1 knockout and liver-specific overexpression mouse models, ectosome isolation, macrophage activation assay |
Molecular therapy. Nucleic acids |
Medium |
35036051
|
| 2024 |
DRAM1 interacts with STIM1 to tether lysosomes to the ER, perturbing STIM1 function in maintaining intracellular calcium homeostasis; excess DRAM1 disrupts ER structure, triggers ER stress, and induces protective ER-phagy. Lysosomal localization of DRAM1 requires its intact cytosol-facing C-terminal domain. STIM1 overexpression restores calcium homeostasis, ER stress response, and AMPK-ULK1 signaling in cells with excess DRAM1. |
Co-immunoprecipitation of DRAM1 and STIM1, calcium imaging, ER morphology analysis, ER-phagy assay, AMPK-ULK1 signaling readouts, domain-deletion mutants for localization |
Proceedings of the National Academy of Sciences of the United States of America |
High |
39292746
|
| 2023 |
In macrophages, DRAM1 localizes to mycobacteria-containing vesicles post-phagocytosis; DRAM1 knockdown reduces LC3 recruitment to mycobacteria and acidification of mycobacteria-containing vesicles, and reduces fusion with LAMP1-positive lysosomes, impairing intracellular killing. |
DRAM1 siRNA knockdown in RAW264.7 macrophages, immunofluorescence co-localization with LC3/LysoTracker/LAMP1, bacterial survival assay |
Cells |
Medium |
36980169
|
| 2024 |
DRAM1 and xenophagy receptors Optn and p62 independently promote host defense against Mycobacterium marinum; Dram1 overexpression can compensate for loss of Optn or p62, and vice versa. Dram1 overexpression restores Lc3-Mm interaction in optn/p62 double mutants, indicating Dram1-mediated defense does not rely on specific xenophagy receptors. |
Single and double knockout zebrafish lines, overexpression rescue experiments, Lc3-Mm co-localization imaging, bacterial burden quantification |
Frontiers in cellular and infection microbiology |
Medium |
38264729
|
| 2025 |
DRAM1 directly binds VAMP8 on lysosomes; this interaction is enhanced upon autophagy induction. DRAM1 competitively inhibits CHIP/STUB1-mediated ubiquitination of VAMP8 at Lys68, Lys72, and Lys75, stabilizing lysosomal VAMP8 and promoting assembly of the STX17-SNAP29-VAMP8 SNARE complex, thereby facilitating autophagosome-lysosome fusion and autophagic flux. DRAM1-mediated VAMP8 stabilization promotes HCC cell extravasation. |
Co-immunoprecipitation of DRAM1-VAMP8 and STUB1-VAMP8, ubiquitination assay, site-directed mutagenesis of VAMP8 lysines, SNARE complex assembly assay, ATG5/ATG7 knockout, mouse and zebrafish metastasis models |
Nature communications |
High |
40595569
|
| 2025 |
DRAM1 activates AMPK and mediates pro-senescent autophagy (DMPA) in response to aging-associated metabolic cues (N-acetylhistamine, phosphatidylethanolamine); DRAM1-mediated autophagy in this context does not notably degrade SQSTM1/p62, distinguishing it from general macroautophagy. |
DRAM1 overexpression/knockdown in human MSCs and mouse hepatocytes, metabolomics, AMPK activity assay, autophagy flux assay, senescence markers, N-AcHA and ethanolamine supplementation |
Autophagy |
Medium |
41037659
|
| 2023 |
Dram1/DRAM1 promotes LC3-associated phagocytosis (LAP) of Salmonella Typhimurium; Dram1 knockdown or mutation reduces GFP-Lc3 association with Salmonella and abolishes phagosomal NADPH oxidase-dependent ROS response to the bacteria. These results were confirmed in zebrafish and murine RAW264.7 macrophages. |
Morpholino knockdown, CRISPR mutation, mRNA overexpression in zebrafish, Salmonella ROS biosensor, GFP-Lc3 imaging, siRNA in RAW264.7 macrophages |
Autophagy reports |
Medium |
40950712
|
| 2012 |
p73-regulated DRAM-1 is functionally required for neutrophil differentiation of APL cells; DRAM-1 expression is induced during ATRA-induced differentiation of NB4 APL cells, and its knockdown impairs this differentiation. p73 inhibition prevents both differentiation and DRAM-1 induction. |
siRNA knockdown of DRAM-1, ATRA differentiation assay, p73 inhibition, DRAM-1 expression measurement by qPCR/Western blot |
Leukemia research |
Medium |
22981223
|
| 2012 |
Serum deprivation induces DRAM expression in liver cancer cells through epigenetic remodeling: active chromatin marks (diacetyl-H3, tetra-acetyl-H4, trimethyl-H3K4) increase and repressive mark (dimethyl-H3K9) decreases at the DRAM core promoter. The chromatin remodeling factor Brg-1 is enriched at the DRAM promoter and is required for serum deprivation-induced DRAM expression. |
ChIP for histone marks and Brg-1 at DRAM promoter, Brg-1 knockdown, luciferase reporter for DRAM promoter activity |
PloS one |
Medium |
23251372
|
| 2025 |
DRAM1 interacts with VAMP8; this interaction is enhanced by autophagy stimulation. DRAM1 preferentially promotes autophagosome-lysosome fusion by enhancing assembly of the STX17-SNAP29-VAMP8 SNARE complex, and inhibits VAMP8 ubiquitination at Lys68, Lys72, and Lys75 by competing with CHIP/STUB1. |
Co-immunoprecipitation, ubiquitination assay, mutagenesis of VAMP8 lysine residues, SNARE complex co-IP, autophagy flux assay |
Autophagy |
High |
40884094
|