| 2000 |
PTIP (PAXIP1) was identified as a novel protein that directly binds to the activation domain of PAX2 (and other Pax proteins) in vitro, in yeast two-hybrid assays, and in tissue culture cells. The octapeptide repression domain of Pax2 inhibits this binding. PTIP contains five BRCT domains and co-localizes with Pax2 in the nucleus at actively expressed chromatin and the nuclear matrix fraction. |
Yeast two-hybrid, in vitro binding, co-immunoprecipitation in tissue culture, nuclear fractionation, co-localization |
Nucleic acids research |
High |
10908331
|
| 2003 |
PTIP is essential for progression through mitosis. PTIP-null mouse embryos show reduced mitosis, widespread cell death, DNA damage preceding nuclear condensation, and defective phospho-histone H3 expression. Neither embryonic fibroblasts nor embryonic stem cells from PTIP mutants proliferate in culture. Trophoblast cells are more sensitive to DNA-damaging agents. |
Constitutive null allele generation in mice, immunostaining for mitotic markers (phospho-H3), DNA damage markers, cell culture proliferation assays |
Molecular and cellular biology |
High |
12588986
|
| 2004 |
Human PTIP (hPTIP) contains 1069 amino acids and six BRCT domains. It shows increased association with 53BP1 in response to ionizing radiation (IR), and this IR-induced association requires ATM. PTIP is required for ATM-mediated phosphorylation of p53 at Ser15 and for IR-induced up-regulation of p21. PTIP depletion increases cellular sensitivity to IR. |
Co-immunoprecipitation, deletion analysis, siRNA knockdown, Western blot for p53-Ser15 phosphorylation and p21, cell survival assays |
The Journal of biological chemistry |
High |
15456759
|
| 2007 |
Endogenous PTIP and a novel protein PA1 are components of a Set1-like histone H3K4 methyltransferase (HMT) complex containing ASH2L, RBBP5, WDR5, hDPY-30, NCOA6, MLL3, MLL4, and UTX. The PTIP complex carries HMT activity specifically methylating H3K4. PA1 binds PTIP directly and requires PTIP for interaction with the rest of the complex. hDPY-30 binds ASH2L directly. |
Co-purification, mass spectrometry, co-immunoprecipitation, in vitro HMT assay, direct binding assays |
The Journal of biological chemistry |
High |
17500065
|
| 2007 |
PTIP bridges the DNA-binding protein PAX2 to the ALR/MLL3/MLL4 H3K4 methyltransferase complex. PAX2 promotes assembly of this complex and H3K4 methylation at a PAX2-binding DNA element through PTIP. Without PTIP, PAX2 binds DNA but fails to assemble the ALR complex. PTIP-null and conditional mutants show reduced H3K4 methylation levels. |
Co-purification, conditional and constitutive knockout mice, chromatin immunoprecipitation (ChIP), H3K4 methylation assays |
Developmental cell |
High |
17925232
|
| 2008 |
PTIP/Swift is required for efficient PCNA ubiquitination and recruitment of TLS polymerase eta to chromatin in response to DNA damage. Immunodepletion of PTIP/Swift from Xenopus egg extracts prevented PCNA ubiquitination and polymerase eta recruitment during replicative stress. PTIP depletion in mammalian cells by RNAi reduced PCNA ubiquitination and decreased recruitment of polymerase eta and Rad51 to chromatin. |
Xenopus egg extract immunodepletion, siRNA knockdown in mammalian cells, chromatin fractionation assays |
DNA repair |
High |
18353733
|
| 2009 |
Recruitment of PTIP to damaged chromatin depends on the DNA damage signaling pathway γH2AX→MDC1→RNF8, which in turn facilitates sustained localization of PA1 to DNA break sites. The N-terminal PA1-binding domain and C-terminal focus-localization domain of PTIP are critical for its DNA damage repair function, which is likely independent of the MLL complexes. |
Co-immunoprecipitation, siRNA knockdown, immunofluorescence for DNA damage foci, domain deletion analysis, cell viability after ionizing radiation |
The Journal of biological chemistry |
High |
19124460
|
| 2009 |
PTIP is required for PPARγ and C/EBPα expression during adipogenesis. PTIP deletion in mouse embryonic fibroblasts markedly decreases PPARγ expression and impairs H3K4 trimethylation and RNA Pol II occupancy at PPARγ and C/EBPα promoters. Rescue of the adipogenesis defect in PTIP-/- MEFs requires co-expression of both PPARγ and C/EBPα. |
Conditional knockout mice, ChIP for H3K4me3 and RNA Pol II, rescue experiments with PPARγ/C/EBPα co-expression, adipogenesis assays |
Cell metabolism |
High |
19583951
|
| 2009 |
RNF8 controls DNA damage-induced nuclear foci formation of PTIP, which in turn regulates 53BP1 localization to DNA damage sites. PTIP is also required for ATM-dependent SMC1 phosphorylation at damage sites. PTIP acts downstream of RNF8 and upstream of 53BP1 in the DNA damage response pathway. |
siRNA knockdown, immunofluorescence for nuclear foci, Western blot for SMC1 phosphorylation, epistasis analysis |
The Journal of biological chemistry |
High |
19414588
|
| 2009 |
Drosophila PTIP ortholog is essential for anterior/posterior patterning and segmentation. Loss of Drosophila ptip decreases global H3K4 methylation and increases H3K27 methylation. Drosophila PTIP is required to activate homeotic gene expression in response to derepression of Polycomb group genes, and binds to promoter sequences coincident with increased H3K4 trimethylation. |
Genetic null alleles in Drosophila, global histone methylation analysis, cell culture reporter assays, ChIP at homeotic gene promoters |
Development (Cambridge, England) |
High |
19429789
|
| 2009 |
PTIP is required to maintain H3K4 methylation in embryonic stem cells. PTIP deletion in ES cells leads to spontaneous differentiation to trophectoderm, loss of pluripotency, reduced Oct4 expression, reduced H3K4 methylation, and impaired differentiation along all three germ layers in embryoid bodies. |
Conditional PTIP knockout in ES cells using Cre recombinase, flow cytometry, immunostaining, ChIP for H3K4 methylation |
Stem cells (Dayton, Ohio) |
Medium |
19544464
|
| 2010 |
PTIP promotes DNA double-strand break repair through homologous recombination (HR). PTIP-deficient chicken DT40 cells show increased spontaneous DNA lesions, sensitivity to IR and camptothecin, and reduced HR efficiency as measured by artificial recombination substrates. PTIP-depleted HeLa cells also show reduced HR efficiency. |
Gene disruption in DT40 cells, HR efficiency assay with recombination substrates, sensitivity assays (IR, camptothecin), siRNA in HeLa cells |
Genes to cells : devoted to molecular & cellular mechanisms |
High |
20088963
|
| 2010 |
PTIP promotes H3K4me3 and transcription initiation at downstream switch regions of the immunoglobulin heavy-chain (Igh) locus in activated B cells. PTIP-deficient B cells show impaired H3K4me3 and transcription at Igh switch regions, leading to defective class switch recombination (CSR). PTIP accumulation at DSBs also contributes to CSR and genome stability independently of Igh switch transcription. |
Conditional B-cell-specific PTIP knockout, ChIP-seq, RNA-seq, class switch recombination assays, flow cytometry |
Science (New York, N.Y.) |
High |
20671152
|
| 2011 |
PTIP is required for long-range chromatin interactions between the 3' regulatory region enhancer and germline transcript promoters at the immunoglobulin heavy chain locus. Loss of PTIP in mature B cells inhibits CSR by suppressing H3K4 methylation at germline transcript promoters, reduces Pax5 binding, and abolishes chromatin looping detected by chromosome conformation capture. |
CD19-Cre conditional PTIP knockout, ChIP, chromosome conformation capture (3C), class switch recombination assays |
Molecular and cellular biology |
High |
21282469
|
| 2011 |
The tandem BRCT5-BRCT6 domain of human PTIP directly recognizes the γH2AX tail, and this interaction depends on phosphorylation of H2AX Ser139. Crystal structure at 2.15 Å resolution of the hPTIP BRCT5/6-γH2AX complex was determined, and mutation analysis confirmed the molecular basis for the interaction. |
X-ray crystallography (2.15 Å resolution), mutagenesis, binding assays |
FEBS letters |
High |
22064073
|
| 2012 |
PAXIP1/PTIP regulates RAG-mediated cleavage and repair during V(D)J recombination in DP thymocytes. Loss of PAXIP1 diminishes Jα H3K4me3 and germline transcription, suppresses DSB formation at 3' Jα segments, and results in accumulation of unresolved Tcra breaks. PAXIP1 is also essential for S1PR1-mediated mature thymocyte egress from the thymus through transcriptional activation of S1pr1. |
Conditional knockout in thymocytes, ChIP for H3K4me3, DSB detection assays (LMPCR), flow cytometry, gene expression analysis |
Immunity |
High |
23159437
|
| 2012 |
The mutant androgen receptor (AR) with poly-glutamine expansion (associated with SBMA) specifically interacts with PTIP and sequesters PTIP away from radiation-induced nuclear foci. This results in increased sensitivity to DNA-damaging agents and chromosomal instabilities. In a mouse model of SBMA, DNA damage is detected in muscle cells and muscular atrophy is accelerated when one copy of PTIP is removed. |
Co-immunoprecipitation, immunofluorescence for nuclear foci, DNA damage assays, mouse genetic model (PTIP heterozygosity in SBMA model) |
Human molecular genetics |
Medium |
22736030
|
| 2014 |
PTIP binds to Artemis nuclease as a PTIP-binding protein. Loss of Artemis restores PARP inhibitor resistance in BRCA1-deficient cells, demonstrating Artemis is a major downstream effector of the 53BP1-PTIP pathway that prevents end resection and promotes NHEJ, directly competing with homologous recombination repair. |
Co-immunoprecipitation, genetic epistasis (double knockout cell lines), PARP inhibitor sensitivity assays, end resection assays |
Genes & development |
High |
25512557
|
| 2014 |
PITX2 associates with the PTIP-containing MLL4/KMT2D histone H3K4 methyltransferase complex. This association is dependent on PITX2's homeodomain. The PITX2 protein complex possesses H3K4 HMT activity, and ChIP shows co-occupancy of PITX2 and PTIP on PITX2 transcriptional target promoters. |
Co-immunoprecipitation, in vitro HMT assay, chromatin immunoprecipitation (ChIP), domain deletion analysis |
Biochemical and biophysical research communications |
Medium |
24486544
|
| 2015 |
The phosphatase PPM1B can dephosphorylate the Pax2 activation domain and displace PTIP, thereby inhibiting H3K4 methylation and gene activation. PPM1B is an essential component of the Groucho4 repressor complex recruited by Pax2. Loss of PPM1B prevents Groucho-mediated gene repression, demonstrating that phosphorylation state of Pax2 controls the switch between PTIP-mediated activation and PPM1B/Groucho-mediated repression. |
Co-immunoprecipitation, phosphatase assays, ChIP, reporter gene assays, siRNA knockdown |
The Journal of biological chemistry |
Medium |
25631048
|
| 2016 |
A PTIP-PA1 subcomplex functions independently from the MLL3/MLL4 complex to mediate transcription and class switch recombination. Using quantitative proteomics in primary lymphocytes, a tandem BRCT domain of PTIP was identified as sufficient for CSR, with PA1 as its main functional partner. PTIP promotes CSR separately from its association with the MLL3/MLL4 complex and from its localization to sites of DNA damage. |
Quantitative proteomics, domain mapping by mutagenesis, B-cell conditional knockout, class switch recombination assays |
Genes & development |
High |
26744420
|
| 2016 |
PAXIP1 BRCT domains interact with WEE1 kinase and regulate WEE1-mediated phosphorylation of CDK1. Ectopic expression of PAXIP1 promotes enhanced caspase-3-mediated apoptosis in cells treated with WEE1 inhibitor AZD1775 and cisplatin. |
Co-immunoprecipitation (BRCT-mediated interaction network), pharmacologic screen, ectopic expression, caspase-3 activity assays |
Molecular cancer therapeutics |
Medium |
27196765
|
| 2021 |
DACH1 interacts with PTIP and is recruited by DACH1 to its promoter-binding sites. DACH1-PTIP recruitment represses transcription and reduces promoter H3K4Me3 levels. DACH1 knockdown in podocytes combined with hyperglycemia triggers target gene upregulation and increased promoter H3K4Me3, revealing that DACH1 uses PTIP-H3K4Me3 activity for transcriptional repression at DACH1 target loci. |
Co-immunoprecipitation, ChIP for H3K4me3, RNA sequencing, conditional knockout mice, siRNA knockdown |
The Journal of clinical investigation |
Medium |
33998601
|
| 2022 |
PTIP governs NAD+ metabolism in macrophages by regulating CD38 expression. PTIP cooperates with acetyltransferase p300 to establish an active intronic enhancer of CD38 with enriched H3K27ac. PTIP deletion impairs proinflammatory response, promotes metabolic switch from glycolysis to oxidative phosphorylation, and alters NAD+ metabolism via downregulating CD38. |
Conditional knockout in macrophages, ChIP for H3K27ac, metabolic profiling (NAD+ measurement), cytokine assays, enhancer identification by ChIP-seq |
Cell reports |
Medium |
35354042
|
| 2022 |
PTIP is essential for proper chromosome segregation during mitosis in HeLa cells. PTIP inactivation results in prolonged mitotic time, inefficient chromosome alignment, and increased cell death during mitotic exit. PTIP localizes to the mitotic centrosome via its C-terminal BRCT domains. |
siRNA knockdown, live-cell imaging, immunofluorescence for centrosome localization, BRCT domain deletion analysis |
Cell division |
Medium |
36153541
|
| 2023 |
PAXIP1 and STAG2 converge to maintain 3D genome architecture and facilitiate promoter-enhancer contacts for glucocorticoid receptor (GR)-dependent transcription. PAXIP1 is required for stability of cohesin on chromatin, cohesin localization to GR-occupied sites, and maintenance of enhancer-promoter interactions. PAXIP1 and STAG2 depletion alter the GR transcriptome without altering the GR cistrome. |
CRISPR genome-wide screen, ChIP-seq for cohesin, ATAC-seq, Hi-C, co-immunoprecipitation, conditional knockdown |
Nucleic acids research |
High |
37070193
|
| 2023 |
PAXIP1 (with binding partner PAGR1) promotes global chromatin association of cohesin independently of DNA replication, transcription, or DNA repair. Depletion of PAXIP1 severely aggravates cohesion defects in ESCO2 mutant cells leading to mitotic cell death. Cohesin regulation by PAXIP1 requires PAGR1 and a conserved FDF motif in PAGR1. PAXIP1 co-localizes with cohesin on active gene promoters and enhancers. |
CRISPR synthetic lethality screens, ChIP-seq for cohesin, co-immunoprecipitation, domain mutagenesis (FDF motif), cohesion assays, live-cell imaging |
Nucleic acids research |
High |
37702151
|
| 2024 |
PTIP undergoes UFMylation in response to replication stress (detected by denaturing co-immunoprecipitation). This post-translational modification promotes end resection and degradation of nascent DNA at stalled replication forks in BRCA1-deficient cells. PTIP-depleted and UFL1-depleted BRCA1 knockdown cells are less sensitive to PARP inhibitors. |
Denaturing co-immunoprecipitation, DNA fiber assays for fork degradation, cell viability assay with PARP inhibitors, siRNA knockdown |
The Journal of biological chemistry |
Medium |
38657865
|
| 2024 |
PTIP is required for H3K4me3 upregulation in an intermediate phase after ionizing radiation and promotes cell cycle arrest by epigenetically inducing PRDM1. PTIP is a component of the MLL histone methyltransferase complex required for this radiation-induced H3K4me3 increase and downstream PRDM1 expression. |
Conditional knockout in hematopoietic cells, ChIP for H3K4me3, gene expression analysis, cell cycle assays after IR |
Scientific reports |
Medium |
39097652
|
| 2024 |
PAXIP1 and PAGR1 are epistatic to STAG2 in oncogenic KRAS-driven lung tumorigenesis in vivo. Gene expression and chromatin accessibility profiles in STAG2- and PAXIP1-deficient neoplastic cells are similar, functionally linking STAG2-cohesin to the PAXIP1/PAGR1 heterodimeric complex as a tumor-suppressive axis. |
Somatic CRISPR-Cas9 in autochthonous mouse lung cancer model, tumor barcoding, RNA-seq, ATAC-seq, genetic epistasis in vivo |
The Journal of experimental medicine |
High |
39345539 39652422
|
| 2025 |
A fraction of PTIP is actively transported from the nucleus to mitochondria, causing mitochondrial aggregation, cytochrome c release into the cytoplasm, and cellular apoptosis. Deletion of an N-terminal glutamine-rich region, mutation of a conserved threonine within BRCT3, and truncation of the C-terminal BRCT5 domain each significantly reduced apoptosis. |
Subcellular fractionation, immunofluorescence for mitochondrial localization, cytochrome c release assay, domain deletion/mutagenesis, apoptosis assays |
Journal of cellular signaling |
Medium |
41608385
|