| 1995 |
RBBP6 (RBQ-1) binds to the retinoblastoma gene product (pRB) through a small region near its C-terminus, as demonstrated by GST pull-down of pRB from cellular extracts, with binding competed by adenovirus E1a protein indicating the interaction occurs through the pocket domain of Rb1. |
GST fusion protein pull-down, competition with E1a protein |
Genomics |
Medium |
8595913
|
| 1997 |
P2P-R (RBBP6) encodes protein domains that bind single-stranded nucleic acids and associate with hnRNP proteins, as demonstrated by binding of cDNA-derived fusion proteins to ssDNA and recognition by anti-hnRNP monoclonal antibodies. |
GST fusion protein binding assay, monoclonal antibody recognition, antisense oligonucleotide experiments |
Proceedings of the National Academy of Sciences of the United States of America |
Medium |
9037032
|
| 2002 |
P2P-R (RBBP6) localizes to nucleoli in interphase cells and to the periphery of chromosomes in mitotic cells, with protein levels increasing >10-fold during mitosis without a concomitant change in mRNA, suggesting post-transcriptional regulation. |
Confocal microscopy, Western blot, mitotic cell synchronization (nocodazole, vinblastine, shake-select) |
Journal of cellular physiology |
Medium |
12064457
|
| 2002 |
Overexpression of near full-length P2P-R (RBBP6) in Saos2 cells restricts mitotic progression at prometaphase and promotes mitotic apoptosis, with P2P-R protein dissociating from chromosomes and appearing in cytoplasm and apoptotic cell surface blebs during mitotic apoptosis. |
Stable transfection, flow cytometry, confocal microscopy, Western blot of enriched apoptotic blebs |
Journal of cellular physiology |
Medium |
12384997
|
| 2002 |
P2P-R (RBBP6) deficiency restricts cell cycle progression from G1 through S to mitosis in a microtubule-dependent manner and represses UV irradiation-induced apoptosis. |
Antisense oligonucleotide knockdown, flow cytometry, nocodazole treatment |
Anticancer research |
Low |
12553003
|
| 2003 |
P2P-R (RBBP6) is phosphorylated by cdc2 and SRPK1a kinases, interacts with scaffold attachment factor-B (SAF-B), and co-immunoprecipitates with nucleolin. |
Co-immunoprecipitation, in vitro kinase assay (inferred from review-style paper) |
Journal of cellular biochemistry |
Low |
12938151
|
| 2003 |
Overexpression of P2P-R (RBBP6) segments spanning residues 1156-1314 promotes camptothecin-induced apoptosis 3-5 fold in MCF-7 cells; the p53-binding domain overlaps with this apoptosis-associated region. |
Stable transfection, flow cytometry, TUNEL assay |
Journal of cellular physiology |
Medium |
14566974
|
| 2005 |
PUM2 binds P2P-R (RBBP6) mRNA through consensus sequences in its 3' UTR, as confirmed by PUM2 pull-down followed by RT-PCR, suggesting translational regulation of RBBP6 by PUM2. |
RNA pull-down (PUM2 immunoprecipitation) followed by RT-PCR |
Journal of cellular physiology |
Low |
15617101
|
| 2005 |
SNAMA, the Drosophila homolog of RBBP6, contains a DWNN domain and a RING finger-like motif; homozygous P-element insertion mutants show embryonic lethality with widespread apoptosis throughout the gastrula, establishing an essential developmental role for this gene family. |
P-element insertion genetics, embryo phenotype analysis |
Biochimica et biophysica acta |
Medium |
15733535
|
| 2006 |
The N-terminal 81 amino acids of RBBP6 form a novel ubiquitin-like domain (DWNN) as determined by heteronuclear NMR; the domain lacks conserved K48/K63 equivalents but contains a di-glycine motif in human/mouse, and is independently expressed as a single-domain protein in vertebrates. |
Heteronuclear NMR structure determination |
BMC structural biology |
High |
16396680
|
| 2008 |
RBBP6 acts as an E3 ubiquitin ligase for YB-1: the RING finger domain of RBBP6 binds the last 62 residues of YB-1 (identified by yeast two-hybrid), and both full-length RBBP6 and the isolated RING finger domain ubiquitinate YB-1 leading to its proteasomal degradation, suppressing YB-1 transactivational activity in vivo. |
Yeast two-hybrid, in vitro ubiquitination assay, proteasome degradation assay, reporter transactivation assay |
Journal of molecular biology |
High |
18851979
|
| 2010 |
P2P-R (RBBP6) functions as a transcriptional co-repressor of estrogen-dependent transcription: it represses estrogen-induced transcription by 50-70% when transfected into four cell types, and co-immunoprecipitates with SRC-1 (steroid receptor co-activator 1) and estrogen receptor alpha. |
Transient transfection reporter assay, antisense knockdown, co-immunoprecipitation |
BMC systems biology |
Medium |
20184719
|
| 2011 |
The RING finger-like domain of RBBP6 adopts a homodimeric structure similar to U-box proteins despite coordinating two zinc ions (replaceable with cadmium); RBBP6 interacts with chaperones Hsp70 and Hsp40 through its N-terminal DWNN ubiquitin-like domain, suggesting a role in chaperone-mediated ubiquitination. |
Solution NMR structure, zinc/cadmium substitution assays, thermal stability assays, yeast two-hybrid |
The Journal of biological chemistry |
High |
22130672
|
| 2013 |
RBPL-1, the C. elegans homolog of RBBP6, is required for germ cell proliferation, oocyte production, embryonic development, and intestine development; RNAi silencing causes embryonic lethality and defects in mitosis, consistent with a role as an mRNA cleavage/polyadenylation factor. |
RNAi knockdown, phenotypic analysis, microarray expression profiling |
PloS one |
Medium |
23536819
|
| 2014 |
RBBP6 ubiquitinates and destabilizes the transcriptional repressor ZBTB38; loss of RBBP6 causes ZBTB38 accumulation, leading to MCM10 downregulation on chromatin, reduced replication fork progression, and increased DNA damage at common fragile sites. |
shRNA knockdown, ubiquitination assay, chromatin fractionation, DNA fiber assay, FISH for fragile site stability |
Cell reports |
High |
24726359
|
| 2014 |
RBBP6 is a component of the mRNA 3' processing complex and functions in 3' processing in vitro and in vivo; its DWNN ubiquitin-like domain mediates interaction with core cleavage/polyadenylation factors and is required for 3' processing activity. RBBP6 isoform 3 (iso3, DWNN-only) competes with full-length RBBP6 for binding to the core machinery, thereby inhibiting 3' processing. RBBP6 knockdown decreases transcript levels of AU-rich 3' UTR mRNAs (e.g., c-Fos, c-Jun) and increases usage of distal poly(A) sites. |
In vitro 3' processing assay, co-immunoprecipitation, genome-wide poly(A) site analysis, siRNA knockdown |
Genes & development |
High |
25319826
|
| 2018 |
RBBP6 interacts with Ebola virus VP30 (transcription regulator) through a 23 amino acid region that mimics the viral nucleoprotein (NP) binding interface on VP30; a crystal structure of the VP30-RBBP6 peptide complex revealed competitive mimicry. RBBP6 knockdown stimulates viral transcription and increases EBOV replication; RBBP6 overexpression inhibits both. |
AP-MS, domain mapping, X-ray crystallography, siRNA knockdown, viral replication assays |
Cell |
High |
30550789
|
| 2019 |
RBBP6 ubiquitinates IκBα (inhibitor of NF-κB), leading to its degradation and consequent p65 nuclear translocation, NF-κB pathway activation, EMT induction, and cancer cell metastasis in colorectal cancer. |
Co-immunoprecipitation, ubiquitination assay, nuclear fractionation, ChIP analysis, loss-of-function/gain-of-function experiments, mouse metastasis model |
Cell death & disease |
Medium |
31685801
|
| 2021 |
The RING finger domain of RBBP6 binds SNRPG (small nuclear ribonucleoprotein polypeptide G) with a dissociation constant of ~3.16 nM as measured by microscale thermophoresis, confirming a physical interaction between these two splicing-related proteins. |
Microscale thermophoresis (MST) binding assay |
American journal of translational research |
Low |
34956492
|
| 2022 |
RBBP6 is required to activate the human CPSF endonuclease for specific and efficient pre-mRNA 3' cleavage; unlike its yeast homolog Mpe1, RBBP6 does not stably copurify with CPSF but is recruited in an RNA-dependent manner. Sequence and mutational analyses indicate RBBP6 interacts with WDR33 and CPSF73 subunits of CPSF. |
In vitro reconstitution of 3' endonuclease activity with purified proteins, mutagenesis, co-purification experiments |
Genes & development |
High |
35177536
|
| 2022 |
RBBP6 is required for pre-mRNA 3' end cleavage in a minimal reconstituted mammalian system; structural data show the RBBP6 DWNN domain contacts and presumably activates the endonuclease CPSF73. RBBP6 is among 14 polypeptides essential for RNA processing in vitro, and its role is conserved from yeast (Mpe1) to humans. |
In vitro reconstitution with 14 purified polypeptides, structural analysis, RNA cleavage assay at physiological poly(A) site |
Genes & development |
High |
35177537
|
| 2024 |
RBBP6 mediates K63-linked ubiquitination of CPSF3 (Cleavage and Polyadenylation Specific Factor 3), which stabilizes CPSF3 and regulates alternative polyadenylation events in glioblastoma stem cells; RBBP6 depletion induces shortening of 3' UTRs of MYC competing-endogenous RNAs, releasing miR-590-3p to decrease MYC expression. |
CRISPR/Cas9 knockout screens, ubiquitination assay (K63-linkage specific), alternative polyadenylation profiling, miRNA-mRNA interaction analysis |
Cell discovery |
Medium |
38503731
|
| 2024 |
RBBP6 promotes K48-linked polyubiquitination of ERRα at the K100 residue, leading to its proteasomal degradation; this contributes to mitochondrial injury in proximal renal tubular cells in diabetic kidney disease. RBBP6 inhibition or ERRα overexpression reduces mitochondrial damage in diabetic mice. |
Co-immunoprecipitation, ubiquitination assay (K48-linkage and site-specific mutagenesis), conditional knockout/overexpression mouse models, cellular fractionation |
Advanced science (Weinheim, Baden-Wurttemberg, Germany) |
Medium |
39441040
|
| 2024 |
Rbbp6 promotes K48-linked ubiquitination and proteasomal degradation of Bmal1, which suppresses the YAP1 signaling pathway and promotes ferroptosis in diabetic testicular damage; co-immunoprecipitation confirmed the Rbbp6-Bmal1 interaction. |
Co-immunoprecipitation, ubiquitination assay, Western blot, ferroptosis marker analysis, knockdown/overexpression experiments |
Diabetes & metabolism journal |
Medium |
39501569
|
| 2024 |
SRSF1-mediated alternative splicing regulates relative levels of RBBP6 isoform 1 vs isoform 3; knockdown of RBBP6 isoform 1 increases p53 protein levels in multiple myeloma cells, consistent with RBBP6 isoform 1 negatively regulating p53 through its ubiquitin ligase activity. |
siRNA knockdown, overexpression, Western blot, CCK-8 proliferation assay, RT-PCR |
Zhongguo shi yan xue ye xue za zhi |
Low |
39743259
|
| 2025 |
RBBP6 inhibits Yellow Fever Virus (YFV) genome replication by interacting with the viral polymerase NS5, identifying RBBP6 as a restriction factor for YFV. |
AP-MS (affinity purification-mass spectrometry), functional viral replication assays |
bioRxivpreprint |
Low |
|
| 2025 |
RBBP6 ubiquitinates and destabilizes FOXP3 via the ubiquitin-proteasome pathway in HBV-related hepatocellular carcinoma; RBBP6 knockdown restores FOXP3 expression and inhibits tumor formation in vivo. RFX5 transcriptionally activates RBBP6 in HBV-positive HCC cells. The interaction between FOXP3 and RBBP6 was confirmed by GST pull-down and co-immunoprecipitation. |
GST pull-down, co-immunoprecipitation, ubiquitination assay, ChIP, dual-luciferase reporter assay, xenograft mouse model |
Pathology, research and practice |
Medium |
40934694
|
| 2026 |
RBBP6 ubiquitinates and degrades STAT1, suppressing DPP4 transcription; KMT2B enhances RBBP6 expression through H3K4me3 modification at the RBBP6 promoter. The RBBP6-STAT1 interaction was confirmed by co-immunoprecipitation and GST pull-down. |
ChIP-re-ChIP assay, co-immunoprecipitation, GST pull-down, ubiquitination assay |
Epigenomics |
Medium |
42011633
|