| 2001 |
SOX7 protein contains a functional transactivation domain in its C-terminus and is able to significantly reduce Wnt/beta-catenin-stimulated transcription in cell-based reporter assays. |
Transactivation domain mapping; TCF/LEF reporter assay |
Nucleic acids research |
Medium |
11691915
|
| 2004 |
SOX7 and SOX17 bind specifically to two SOX-binding sites within the laminin alpha1 (Lama1) parietal endoderm-specific enhancer and trans-activate Lama1 transcription in F9 cells; this activation is HMG-box-dependent and synergistic with Sp1/Sp3 and NF-Y binding sites upstream. |
EMSA, luciferase reporter assay, mutational analysis, Northern blot |
The Journal of biological chemistry |
High |
15220343
|
| 2004 |
SOX7 competes with GATA-4 for occupancy of the PS4A element in the Fgf-3 promoter and acts as a potent activator of Fgf-3 transcription; RNAi knockdown of Sox7 in GATA-4-deficient embryoid bodies virtually abolishes Fgf-3 expression. |
Luciferase reporter assay, EMSA, siRNA knockdown, in situ hybridization |
The Journal of biological chemistry |
High |
15082719
|
| 2004 |
In F9 embryonal carcinoma cells, Sox7 acts upstream of Gata-4 and Gata-6 to regulate parietal endoderm differentiation; siRNA silencing of Sox7 blocks induction of Gata-4 and Gata-6 by retinoic acid/cAMP, while overexpression of Gata-4 or Gata-6 in Sox7-silenced cells restores differentiation. |
siRNA knockdown, overexpression, morphological analysis, Western blot, RT-PCR |
Molecular and cellular biology |
High |
15542856
|
| 2005 |
In Xenopus, SOX7 and SOX18 function redundantly to induce cardiogenesis through Xnr2 (nodal) signaling; SOX7 RNA rescues the SOX18 morpholino phenotype and vice versa. Versions of SOX7 with the C-terminal beta-catenin interaction domain replaced by a transcriptional activator still induce cardiogenesis, indicating beta-catenin interaction is dispensable for this activity. |
mRNA injection, morpholino knockdown, animal cap explant assay, marker gene expression |
Developmental dynamics |
High |
16193513
|
| 2007 |
In zebrafish, sox7 and sox18 play redundant but collectively essential roles in establishing arteriovenous identity; simultaneous morpholino knockdown of both genes causes arteriovenous fusions with failure of venous endothelial cell differentiation while endothelial specification is maintained. |
Morpholino knockdown, transgenic line imaging, in situ hybridization with arteriovenous markers |
Blood |
High |
18094332
|
| 2008 |
Zebrafish Sox7 and Sox18 control arterial-venous identity by regulating Gridlock (Hey2) expression; double morphants display ectopic venous marker Flt4 in the dorsal aorta and loss of artery-specific markers EphrinB2a and Gridlock. |
Morpholino knockdown, in situ hybridization, gene expression analysis |
Developmental biology |
High |
18377889
|
| 2008 |
SOX7 protein physically interacts with beta-catenin and suppresses beta-catenin-mediated transcription by depleting active beta-catenin; promoter hypermethylation silences SOX7 in prostate and colorectal cancers. |
Co-immunoprecipitation, luciferase reporter assay, bisulfite sequencing, ectopic expression |
Molecular cancer research |
Medium |
18819930
|
| 2009 |
SOX7 and SOX17 can functionally substitute for SOX18 during lymphatic development in a strain-specific compensatory mechanism; they are activated specifically in the absence of SOX18 function in permissive strains. |
Genetic mouse model, conditional deletion, in vitro and in vivo functional substitution assays |
Development (Cambridge, England) |
High |
19515696
|
| 2009 |
Sustained Sox7 expression in the earliest committed hematopoietic precursors (during ES cell differentiation) promotes maintenance of multipotent self-renewing status and blocks differentiation; removal of the Sox7 block leads to efficient erythroid and myeloid differentiation. |
Inducible Sox7 overexpression in ES cell differentiation system, flow cytometry, colony assays |
Blood |
Medium |
19801444
|
| 2012 |
SOX7 binds and activates the VE-cadherin promoter in haemogenic endothelium; enforced SOX7 expression in haemangioblast-derived blast colonies blocks blood cell differentiation and sustains endothelial marker expression. |
Chromatin immunoprecipitation, luciferase reporter assay, ES cell differentiation gain-of-function |
Development (Cambridge, England) |
High |
22492353
|
| 2012 |
Haploinsufficiency of Sox7 in mice causes anterior retrosternal diaphragmatic hernias; homozygous Sox7 null embryos die with cardiovascular failure. SOX7 is expressed in vascular endothelial cells of the developing diaphragm. |
Targeted gene deletion (Sox7 exon 2 deletion), immunohistochemistry, mouse phenotyping |
Human molecular genetics |
High |
22723016
|
| 2014 |
ETV2 directly binds to ETV2 binding elements in the Sox7 upstream regulatory region and activates Sox7 transcription; Sox7 overexpression mimics ETV2 in promoting endothelial progenitor expansion, and Sox7 knockdown blocks ETV2-induced endothelial progenitor formation and angiogenic sprouting. |
ChIP, luciferase reporter assay, shRNA knockdown, embryoid body differentiation assay |
Stem cells and development |
High |
24762086
|
| 2015 |
In zebrafish, sox7 mutants display arteriovenous shunt formation at specific arterial sites due to ectopic flt4 expression; genetic interaction experiments place Sox7 upstream of Notch (overexpression of Notch intracellular domain rescues sox7 mutant phenotype), and Sox7 interacts genetically with hey2 and efnb2 in arterial specification. |
Zebrafish sox7 mutant generation, in vivo imaging, in situ hybridization, genetic epistasis (NICD overexpression rescue), combinatorial mutant analysis |
Development (Cambridge, England) |
High |
25834021
|
| 2015 |
In the mouse retina, Sox7 and Sox17 reciprocally regulate each other's expression; combined deletion of Sox7, Sox17, and Sox18 causes loss of arterial identity (loss of radial arteries/veins, dense capillary plexus), while a single Sox17 allele largely restores arterial identity. SoxF gene expression is reduced by loss of Norrin/Frizzled4-mediated Wnt signaling but not by VEGF signaling. |
Conditional vascular endothelial-specific gene deletion, retinal whole-mount imaging, molecular marker analysis, genetic interaction with Wnt and VEGF pathway mutants |
PloS one |
High |
26630461
|
| 2016 |
SOX7 directly interacts with RUNX1 and inhibits its transcriptional activity; SOX7 hinders RUNX1 DNA binding and also disrupts the interaction between RUNX1 and its co-factor CBFβ in haemogenic endothelium. |
Co-immunoprecipitation, protein-protein interaction assays, single-cell expression profiling, immunofluorescence, functional reporter assays |
Development (Cambridge, England) |
High |
27802172
|
| 2016 |
PDGF-BB activates SOX7 transcription factor in pericytes, which in turn drives IL-33 expression (the highest upregulated gene); IL-33 promotes metastasis through recruitment of tumour-associated macrophages via the ST2 receptor. |
Gain- and loss-of-function experiments in xenograft mouse models, pharmacological and genetic inhibition of IL-33-ST2, gene expression analysis |
Nature communications |
Medium |
27150562
|
| 2016 |
In tumor endothelial cells of high-grade glioma, Sox7 promotes VEGFR2 expression and vascular abnormality; Sox7 deletion suppresses VEGFR2 expression and normalizes vessels, while Sox17 deletion exacerbates this by up-regulating Sox7. |
Conditional endothelial Sox7 deletion, Sox17 deletion, anti-VEGFR2 antibody treatment, tumor growth assays, gene expression analysis |
The Journal of experimental medicine |
High |
29444818
|
| 2016 |
SOX7 inhibits Wnt/beta-catenin transcriptional activity in acute myeloid leukemia cells through direct protein binding to beta-catenin; deletion of the beta-catenin binding site of SOX7 significantly reduces its anti-leukemia effects. |
Co-immunoprecipitation, domain deletion mutant functional assay, xenogeneic transplantation, overexpression in leukemia cell lines and primary AML cells |
Blood |
High |
25940713
|
| 2016 |
In endometrial cancer cells, Sox7 physically interacts with both wild-type and mutant beta-catenin as well as TCF4, and co-localizes with them in the nucleus; Sox7 inhibits TCF/LEF-1-dependent Wnt transcription and suppresses Wnt targets Cyclin D1 and c-Myc. |
Co-immunoprecipitation, immunofluorescence co-localization, luciferase reporter assay, Western blot |
Oncotarget |
Medium |
23295859
|
| 2017 |
SOX7 suppresses Wnt signaling by competing with BCL9 to bind beta-catenin, thereby disrupting the beta-catenin/BCL9 interaction required for oncogenic transcription. |
Co-immunoprecipitation, SuperTOPFLASH reporter assay |
DNA and cell biology |
Medium |
29271667
|
| 2017 |
Sox7 binds directly to the promoters of Wnt4 and Bmp2 in the atrioventricular canal; Sox7 deficiency in mice reduces Bmp2 expression in AV canal myocardium and Wnt4 in endocardium, impairing endothelial-to-mesenchymal transition (EndMT) required for atrioventricular cushion development. WNT4 or BMP2 protein partially rescues impaired EndMT caused by Sox7 deficiency. |
Conditional Sox7 knockout mice, ChIP (direct binding), transcriptome analysis, rescue experiments with recombinant WNT4/BMP2 protein |
Cell death & disease |
High |
33846290
|
| 2017 |
GATA4 directly and specifically induces Sox7 (and Sox18) expression during cardiomyogenesis; Gata4 knockdown reduces Sox7/Sox18 expression and the cardiomyocyte differentiation defect can be partially restored by reinstating Sox7 or Sox18. |
Genome-wide transcriptomics in Xenopus and mouse ESCs, morpholino/shRNA knockdown, mRNA rescue, RT-PCR |
Developmental biology |
High |
29229250
|
| 2017 |
SOX7 directly binds to the PSMA enhancer (PSME) at SOX box sites #2 and #4 and suppresses PSME-mediated transcription; the nuclear localization signal (NLS) region of SOX7, but not its beta-catenin interacting motif, is essential for this suppressive activity. |
ChIP, EMSA, luciferase reporter assay, domain deletion mutants, stable expression in cancer cell lines |
The Prostate |
High |
30488457
|
| 2017 |
SOX7 directly binds to the HBV core promoter (HBVCP) and competitively displaces hepatocyte nuclear factor 4α to inhibit HBVCP transcription; stapled SOX7 HMG-box peptide mimetics recapitulate this inhibition in HBV-infected primary human hepatocytes. |
EMSA, luciferase reporter assay, pgRNA/HBcAg/cccDNA measurement, stapled peptide experiments in primary hepatocytes |
Journal of hepatology |
High |
28887167
|
| 2018 |
SOX7 induces cellular apoptosis through upregulation of P38 and apoptotic signaling pathway genes, and prevents proteasome-mediated degradation of pro-apoptotic protein BIM. Proteasome inhibitors or MEK/ERK inhibitors attenuate SOX7-promoted BIM degradation. |
Gene expression analysis, pharmacological inhibition (MG132, bortezomib, U0126), Western blot, loss-of-function experiments |
Oncogene |
Medium |
31332289
|
| 2018 |
SOX7 chromatin immunoprecipitation identifies SPRY1 and SLIT2 as direct SOX7-activated target genes, and TRIB3 and MTHFD2 as SOX7-repressed targets in breast cancer cells; these contribute to SOX7-mediated tumor suppression. |
Microarray gene expression profiling, ChIP assay, quantitative PCR validation, correlation with clinical dataset |
International journal of molecular sciences |
Medium |
29757932
|
| 2019 |
SOX7 directly regulates cardiovascular progenitor cell fate by interfering with GATA4 transcriptional activity; protein-protein interaction between SOX7 and GATA4 was demonstrated, and Sox7 modulates WNT and BMP signaling during cardiovascular differentiation. ChIP-Seq and ATAC-Seq defined genome-wide Sox7 target genes in cardiac and endothelial progenitors. |
ChIP-Seq, ATAC-Seq, transcriptomics, Co-IP (protein-protein interaction), doxycycline-inducible ES cell system |
Stem cells and development |
High |
31154937
|
| 2019 |
In hippocampal neurons, SOX7 overexpression promotes apoptosis by interacting with beta-catenin and suppressing its transcriptional activity (not through protein degradation); beta-catenin inhibition mediates the pro-apoptotic effect of SOX7 in potassium deprivation-induced neuronal apoptosis. |
Co-immunoprecipitation, overexpression/knockdown, apoptosis assays, reporter assay |
The European journal of neuroscience |
Medium |
25847511
|
| 2019 |
Sox7 plays a role in antibody-dependent endothelial cell activation via the Jagged1-Notch1 pathway; Sox7 knockdown reduces HLA antibody-induced expression of adhesion molecules and cytokines, and Jagged1 overexpression rescues the inhibitory effects of Sox7 knockdown. |
shRNA knockdown, overexpression, in vitro HKGEC model, in vivo kidney transplantation model, Western blot |
Experimental cell research |
Medium |
30639059
|
| 2017 |
SOX7 is expressed in FLK1-expressing vascular progenitor cells and its deletion causes defective vascular organization from E8.5 onward; conditional deletion of Sox7 in FLK1+ cells leads to widespread vascular defects by E10.5, while VAV-specific Sox7 deletion does not affect haematopoiesis. |
Conditional knockout mice (FLK1-Cre and VAV-Cre), embryo phenotyping, immunostaining, endothelial marker analysis |
Mechanisms of development |
High |
28577909
|
| 2020 |
SOX7 depletion in human endothelial cells impairs hypoxia-induced angiogenesis; SOX7 expression is rapidly and transiently induced during hypoxia through HIF-dependent mechanisms, and is an early regulator of the angiogenic transcriptional program. |
RNA-Seq, SOX7 siRNA depletion, functional angiogenesis assays, HIF1A/EPAS1 depletion for pathway positioning |
The Journal of biological chemistry |
Medium |
32071080
|
| 2021 |
SOX7 directly up-regulates VE-cadherin by binding to its gene promoter in endothelial cells, thereby suppressing EndMT during outflow tract development. SOX7 mutations found in congenital heart disease patients weaken transactivation of the VE-cadherin promoter. |
Luciferase reporter assay, EMSA, collagen gel EndMT assay, overexpression experiments, patient variant functional analysis |
Clinical science |
High |
33720353
|
| 2022 |
A truncating SOX7 variant (Gln104*) fails to transactivate its target genes GATA4 and BMP2, and also loses the ability to cooperatively transactivate with NKX2.5, establishing GATA4, BMP2, and cooperative NKX2.5 interaction as functionally important targets of SOX7 in cardiac development. |
Dual-luciferase reporter assay with wild-type and mutant SOX7, co-transfection with NKX2.5 |
American journal of translational research |
Medium |
35422912
|
| 2023 |
SOX7 in blood vascular endothelial cells (BECs) directly represses VEGFC transcription by binding to distant regulatory regions of the Vegfc locus, and SOX7 directly binds HEY1, a Notch pathway repressor, suggesting recruitment of HEY1 at Vegfc regulatory regions. Endothelial-specific loss of SOX7 causes dysmorphic dermal lymphatic phenotype through non-cell-autonomous regulation of lymphatic patterning. |
Conditional endothelial Sox7 knockout mouse, identification of Vegfc regulatory regions, ChIP/binding assays, Co-IP for SOX7-HEY1 interaction |
The EMBO journal |
High |
36715213
|
| 2023 |
Endothelial-specific loss of Sox7 in mice causes ventricular non-compaction cardiomyopathy with abnormal coronary artery formation; Sox7 maintains cardiac endothelial identity by regulating the Notch pathway and connexins 37 and 40 for coronary arterial specification. Sox7-null endothelial cells transdifferentiate into hematopoietic lineages; single-nuclei transcriptomics identifies depletion of Sox9/Gpc3-positive endocardial progenitors. |
Endothelial-specific conditional KO, single-nuclei transcriptomics, fate mapping, histology |
EMBO reports |
High |
37551717
|
| 2024 |
SOX7 binds to the promoter of DNMT3B and transcriptionally inhibits DNMT3B expression, resulting in reduced methylation of the CYGB promoter and inhibiting bladder cancer progression. |
ChIP assay (SOX7 binding to DNMT3B promoter), bisulfite sequencing (CYGB methylation), overexpression/knockdown, in vivo tumor models |
Molecular biomedicine |
Medium |
39227479
|
| 2016 |
In hepatocellular carcinoma cells, Sox7 physically binds with beta-catenin and TCF4 in the nucleus and inhibits the activity of Wnt/beta-catenin signaling pathway; miR-452 promotes stem-like characteristics by directly targeting Sox7. |
Co-immunoprecipitation, luciferase reporter assay, in vitro and in vivo stem-like cell assays |
Oncotarget |
Medium |
27058905
|
| 2018 |
Sox7 knockdown in primary myoblasts causes impaired myoblast fusion and increased sensitivity to apoptosis; conditional Sox7 knockout in PAX3+ cells in vivo reduces the satellite cell population from birth, reduces myofiber caliber, and impairs muscle regeneration after injury. |
Conditional knockout mouse (PAX3-Cre), shRNA knockdown in primary myoblasts, ES cell differentiation, in vivo injury model |
Stem cell reports |
High |
28943254
|
| 2024 |
SOX7 attenuates hepatic stellate cell (HSC) activation and liver fibrosis by decreasing beta-catenin expression and reducing TGF-β1-induced phosphorylation of Smad2 and Smad3; AAV8-SOX7 overexpression in mice ameliorates CCl4-induced liver fibrosis in vivo. |
AAV8-mediated overexpression in mouse fibrosis model, siRNA knockdown, Western blot, in vivo CCl4 model |
FASEB journal |
Medium |
39126242
|
| 2011 |
SOX7 is upregulated by aspirin in colorectal cancer cells via the p38MAPK pathway; AP1 transcription factors c-Jun and c-Fos upregulate SOX7 promoter activity, and SOX7 mediates aspirin-induced growth inhibition. |
Luciferase reporter assay, p38MAPK inhibition (SB203580), RT-PCR, Western blot, MTT assay |
World journal of gastroenterology |
Medium |
22171135
|