| 2014 |
CTDSP1 (SCP1) physically associates with REST immunocomplexes, dephosphorylates REST at phosphoserines 861/864 (a proline-directed phosphorylation motif), and thereby stabilizes REST protein levels. Mutation at S861/864 stabilizes REST and inhibits its degradation, while CTDSP1 counteracts ERK1/2-mediated phosphorylation that promotes REST degradation via Pin1 and βTrCP. |
Co-immunoprecipitation of CTDSP1 in REST immunocomplexes, phosphatase activity assay on REST peptide substrates, site-directed mutagenesis of S861/864, neural progenitor REST peptide overexpression assay for neuronal differentiation inhibition |
Proceedings of the National Academy of Sciences of the United States of America |
High |
25197063
|
| 2018 |
SCP1/CTDSP1 dephosphorylates two degron phosphosites of REST with a clear kinetic preference for phosphoserine 861 (pSer-861). Crystal structure of SCP1 was obtained and shows direct engagement with REST degron sites. SCP1 stabilizes REST protein levels and sustains REST gene-silencing function in HEK293 cells. |
Kinetic phosphatase assay, X-ray crystallography of SCP1 with REST substrate, REST stability assay in HEK293 cells |
The Journal of biological chemistry |
High |
30217818
|
| 2017 |
SCP1/CTDSP1 localizes to the plasma membrane in cancer cells via palmitoylation of a conserved cysteine motif in its NH2 terminus. Membrane-localized SCP1 dephosphorylates AKT at serine 473, suppressing angiogenesis and tumor growth. Ctdsp1 knockout mice show increased AKT phosphorylation, angiogenesis, and tumorigenesis. |
EGFP/epitope-tagged SCP1 live-cell imaging and fractionation, palmitoylation site mutagenesis, in vitro AKT dephosphorylation assay, Ctdsp1 knockout mouse model with AKT phosphorylation and angiogenesis readouts |
eLife |
High |
28440748
|
| 2011 |
CTDSP1 and its family members (CTDSP2, CTDSPL) synergistically decrease the phosphorylated form of pRb (ppRb) and block G1/S-phase progression. Both CTDSP family members and miR-26a/b are co-expressed during cell cycle quiescence and are downregulated during proliferation. |
Gain- and loss-of-function assays in primary fibroblasts, serum starvation-stimulation cell cycle assays, partial hepatectomy in mice, ppRb quantification by Western blot |
Nucleic acids research |
Medium |
22210897
|
| 2019 |
CTDSP1 overexpression in A549 lung adenocarcinoma cells significantly slows growth and induces senescence, mediated through dephosphorylation of Rb at Ser807/811, Ser780, and Ser795 (increasing the proportion of active, hypophosphorylated Rb). |
CTDSP1 transfection/overexpression in A549 cells, Western blot for Rb phosphorylation at specific sites, cell growth and senescence assays |
Bioscience reports |
Medium |
31774910
|
| 2020 |
CTDSP1 acts as a primary upstream regulator of DNA-PKcs in response to topoisomerase I (topoI) inhibitors including irinotecan. CTDSP1 promotes irinotecan sensitivity by preventing rapid topoI degradation; knockdown of CTDSP1 accelerates topoI degradation and confers drug resistance. Rabeprazole inhibits CTDSP1 activity and thereby promotes resistance to irinotecan. |
Differentially expressing CTDSP1 cell lines, irinotecan sensitivity assays, topoI degradation measurement, CTDSP1 activity assay with rabeprazole, retrospective patient analysis |
PloS one |
Medium |
32764831
|
| 2004 |
CTDSP1 (human NLI-IF/GIP) co-immunoprecipitates with both golli-MBP and nuclear LIM interactor (NLI) under physiological conditions in PC12 cells and N19 cells. CTDSP1 is predominantly nuclear and forms a complex with golli and NLI, linking it to NLI-associated transcriptional regulation. |
Yeast two-hybrid screen, co-immunoprecipitation from PC12 and N19 cell lysates, immunocytochemistry, Northern blot |
Journal of neuroscience research |
Medium |
14743429
|
| 2021 |
CTDSP1 knockdown in mesenchymal progenitor cells (MPCs) and dorsal root ganglion (DRG) neurons promotes neurotrophic factor (including BDNF) expression and promotes DRG neuron regeneration (neurite outgrowth). This mechanism is mediated through CTDSP1's role in stabilizing REST, which suppresses neurotrophic gene expression. |
siRNA knockdown of CTDSP1 in MPCs and DRG neurons, RT-qPCR, Western blot, BDNF ELISA, neurite outgrowth measurement |
Scientific reports |
Medium |
34262056
|
| 2021 |
GPC5 transcriptionally upregulates CTDSP1 expression via the AhR-ARNT pathway, and the resulting CTDSP1 upregulation contributes to inhibited lung cancer cell proliferation. |
GPC5 overexpression in lung cancer cells, reporter assays for AhR-ARNT pathway activation, CTDSP1 expression quantification, cell proliferation assays |
Oncogene |
Medium |
34079082
|
| 2023 |
CTDSP1 overexpression in Caki-1 clear cell renal cell carcinoma cells inhibits cell growth in vitro. This tumor-suppressive activity is consistent with CTDSP1's role in Rb dephosphorylation. |
Transfection of CTDSP1 expression construct into Caki-1 cells, cell growth assays, correlation analysis with RB1 expression in primary tumors |
International journal of molecular sciences |
Low |
37629167
|
| 2016 |
Reduction of Ctdsp1 levels in Müller glia (via miR-124-9-9* overexpression) is associated with decreased REST pathway activity and facilitated neuronal reprogramming. This places CTDSP1 in the REST pathway as a repressor of neuronal gene expression in glia. |
Lentiviral miR-124-9-9* overexpression in murine Müller glia cultures, gene expression analysis, immunofluorescence for neuronal markers, Ctdsp1 protein level quantification |
Glia |
Low |
26732729
|
| 2025 |
Human CTDSP1 (along with CTDSP2 and CTDSPL) can functionally replace yeast Psr1/Psr2 HAD-type phosphatases in restoring TORC1 inhibition and autophagy induction in response to low leucine conditions in Saccharomyces cerevisiae, demonstrating conservation of phosphatase function across species in the TORC1 signaling pathway. |
Genetic complementation assay in yeast (Psr1/Psr2 deletion strains expressing human CTDSP1), TORC1 activity and autophagy measurements |
Autophagy |
Medium |
40103213
|
| 2023 |
CTDSP1 directly suppresses AKT phosphorylation; overexpression of CTDSP1 in neuronal cells exacerbates apoptosis and axonal damage and suppresses AKT phosphorylation under oxygen-glucose deprivation conditions, while miR-124-3p (which targets CTDSP1 3'-UTR) reverses these effects. Dual-luciferase reporter assay confirmed CTDSP1 is a direct target of miR-124-3p. |
Adenovirus-mediated CTDSP1 overexpression, dual-luciferase reporter assay for miR-124-3p targeting CTDSP1 3'-UTR, flow cytometry for apoptosis, immunofluorescence, Western blot for p-AKT |
Cellular and molecular neurobiology |
Medium |
37106272
|
| 2002 |
CTDSP1 (NLI-IF) gene was identified adjacent to NRAMP1 on chromosome 2q35, encoding a 261-amino acid nuclear protein of 29.2 kDa with ubiquitous expression. Northern blot revealed a 2.6-kb transcript ubiquitously expressed across 15 tissues and a 7-kb placenta-specific transcript. |
Genomic sequencing, Northern blot analysis of 15 human tissues |
Mammalian genome |
Low |
10967134
|
| 2022 |
miR-574-5p negatively regulates CTDSP1 by directly targeting CTDSP1; overexpression of miR-574-5p promotes ESCC cell proliferation in a CTDSP1-dependent manner, confirmed by luciferase reporter assay and rescue experiment. |
Dual-luciferase reporter assay, Western blot, RTCA proliferation assay, EdU assay, rescue experiment with CTDSP1 re-expression |
Iranian journal of basic medical sciences |
Low |
36311195
|