| 2001 |
SOX7 protein contains a functional transactivation domain in its C-terminus and can significantly reduce Wnt/β-catenin-stimulated transcription, indicating it acts as a repressor of Wnt signaling. |
Transactivation domain mapping; reporter assay for Wnt/β-catenin transcription |
Nucleic acids research |
Medium |
11691915
|
| 2004 |
SOX7 and SOX17 bind to two SOX-binding sites within the parietal endoderm-specific enhancer of the mouse laminin alpha1 (Lama1) gene via their HMG boxes, and synergistically transactivate this enhancer in cooperation with ubiquitous factors Sp1/Sp3 and NF-Y. |
EMSA, mutational analysis, luciferase reporter assay, Northern blot |
The Journal of biological chemistry |
High |
15220343
|
| 2004 |
SOX7 is a potent transcriptional activator of Fgf-3 through binding to the PS4A regulatory element of the Fgf-3 promoter; SOX7 competes with GATA-4 for PS4A occupancy, and siRNA-mediated knockdown of Sox7 abolishes Fgf-3 expression in GATA-4-deficient embryoid bodies. |
Luciferase reporter assay, nuclear extract binding, RNA interference, in situ hybridization |
The Journal of biological chemistry |
High |
15082719
|
| 2004 |
Sox7 silencing in F9 embryonal carcinoma cells inhibits retinoic acid/cAMP-induced upregulation of Gata-4 and Gata-6, and inhibits parietal endoderm differentiation; Sox7 acts upstream of Gata-4 and Gata-6, and overexpression of either GATA factor rescues differentiation in Sox7-silenced cells. |
siRNA knockdown, Western blot, morphological analysis, laminin-1 production assay, rescue overexpression |
Molecular and cellular biology |
High |
15542856
|
| 2005 |
In Xenopus, SOX7 and SOX18 are redundantly required for cardiogenesis; versions of SOX7 and SOX18 with their C-terminal β-catenin interaction domains replaced by a transcriptional activator still induce cardiogenesis, indicating the cardiogenic function is independent of β-catenin antagonism. |
Morpholino knockdown, RNA overexpression, domain-swap mutant injection, animal cap explant assay |
Developmental dynamics |
High |
16193513
|
| 2007 |
Zebrafish sox7 and sox18 play redundant but collectively essential roles in establishing arteriovenous identity in endothelial cells; simultaneous morpholino knockdown of both genes causes multiple arteriovenous fusions with failure of venous endothelial cell differentiation, while endothelial cell specification is preserved. |
Morpholino knockdown, transgenic reporter lines, in situ hybridization for arterial/venous markers |
Blood |
High |
18094332
|
| 2008 |
Zebrafish Sox7 and Sox18 control arterial-venous identity by regulating Gridlock expression; loss of both genes causes ectopic expression of venous marker Flt4 in the dorsal aorta and loss of artery-specific markers EphrinB2a and Gridlock. |
Morpholino double knockdown, in situ hybridization, transgenic reporter lines |
Developmental biology |
High |
18377889
|
| 2008 |
SOX7 protein physically interacts with β-catenin and suppresses β-catenin-mediated transcription by depleting active β-catenin; Sox7 promoter is hypermethylated in prostate and colorectal cancers, and ectopic SOX7 suppresses proliferation in colorectal cancer cells with endogenous mutant β-catenin. |
Co-immunoprecipitation, reporter assay, bisulfite sequencing, cell proliferation/colony formation assays |
Molecular cancer research |
High |
18819930
|
| 2009 |
Sox7 and Sox17 are strain-specific modifiers that can functionally substitute for Sox18 in lymphatic development in vitro and in vivo; they are not normally expressed during lymphatic development but are specifically upregulated in the absence of Sox18 function in permissive strains. |
In vitro functional substitution assay, in vivo genetic analysis across mouse strains, gene expression analysis |
Development |
High |
19515696
|
| 2009 |
Sox7 sustained expression in earliest committed hematopoietic precursors (from mouse ES cell differentiation) promotes maintenance of multipotent, self-renewing status and blocks differentiation; removal of this block permits efficient differentiation to erythroid and myeloid lineages. Sox7 knockdown decreases formation of primitive erythroid and definitive hematopoietic progenitors. |
Inducible overexpression, siRNA knockdown, ES cell differentiation assay, colony forming assay |
Blood |
High |
19801444
|
| 2009 |
Sox7 and Sox15 both upregulate muscle precursor markers Pax3/7, Meox1, and Foxc1 in P19 cells, but only Sox7 is sufficient to drive full skeletal myocyte differentiation; Sox15 blocks progression past the precursor stage through sustained Msx1 and Id1 expression. |
Stable overexpression in P19 cells, qRT-PCR, immunofluorescence for myogenic markers, dominant-negative analysis |
Stem cells |
Medium |
19489079
|
| 2012 |
SOX7 is expressed in haemogenic endothelium cells during haemangioblast differentiation and its enforced expression blocks further differentiation toward blood precursors while sustaining endothelial markers; SOX7 directly binds and activates the promoter of VE-cadherin, identifying it as a transcriptional target. |
Gain-of-function in mouse ES cell differentiation, chromatin immunoprecipitation (ChIP), promoter-reporter assay, flow cytometry |
Development |
High |
22492353
|
| 2012 |
Sox7 haploinsufficiency in mice causes anterior diaphragmatic hernias; SOX7 is expressed in vascular endothelial cells of the developing diaphragm. Complete Sox7 knockout leads to embryonic lethality with dilated pericardial sacs and failure of yolk sac remodeling indicating cardiovascular failure. |
Targeted gene deletion (exon 2), immunohistochemistry, phenotypic analysis |
Human molecular genetics |
High |
22723016
|
| 2014 |
ETV2 is a direct upstream transcriptional regulator of Sox7; ETV2 binds to ETV2 binding elements in the Sox7 upstream regulatory region and activates transcription. SOX7 overexpression mimics ETV2 in promoting endothelial progenitor cell formation and angiogenic sprouting, while Sox7 knockdown blocks ETV2-induced endothelial progenitor increases. |
ChIP of ETV2 at Sox7 regulatory region, reporter assay, overexpression and shRNA knockdown in embryoid bodies |
Stem cells and development |
High |
24762086
|
| 2015 |
Combined deletion of Sox7, Sox17, and Sox18 in mouse retinal vascular endothelium leads to a dense capillary plexus with near-complete loss of radial arteries and veins; individual deletions have minimal effect due to overlapping function and reciprocal transcriptional regulation between Sox7 and Sox17. |
Conditional endothelial-specific gene deletion, retinal flatmount analysis, vascular smooth muscle cell coverage assay |
PloS one |
High |
26630461
|
| 2015 |
In zebrafish, sox7 mutants display aberrant arteriovenous connections and arterial block; genetic interaction studies show sox7 works with hey2 and efnb2 for arterial specification, and overexpression of Notch intracellular domain rescues the sox7 mutant phenotype, placing Sox7 upstream of Notch in arterial development. |
Zebrafish genetic mutants, in vivo imaging, in situ hybridization, genetic epistasis/rescue with NICD overexpression |
Development |
High |
25834021
|
| 2015 |
SOX7 directly binds β-catenin protein and inhibits Wnt/β-catenin transcriptional activity in AML cells; deletion of the β-catenin binding site in SOX7 significantly reduces its anti-leukemia effects, and SOX7 expression abrogates leukemia engraftment in xenograft transplantation. |
Co-immunoprecipitation, domain deletion mutant, xenograft transplantation, reporter assay |
Blood |
High |
25940713
|
| 2016 |
SOX7 directly interacts with RUNX1 and inhibits its transcriptional activity by hindering RUNX1 DNA binding and blocking the interaction between RUNX1 and its co-factor CBFβ; this mechanism regulates hemogenic endothelium differentiation in the yolk sac. |
Co-immunoprecipitation, ChIP, single-cell expression profiling, immunofluorescence |
Development |
High |
27802172
|
| 2016 |
SOX7 acts as a transcription factor to upregulate IL-33 in pericytes upon PDGF-BB stimulation; IL-33 is the highest upregulated gene following SOX7 activation, and this IL-33-ST2-dependent pathway promotes macrophage recruitment and cancer metastasis. |
Gain- and loss-of-function experiments, gene expression analysis, pharmacological inhibition of IL-33-ST2, xenograft mouse models |
Nature communications |
Medium |
27150562
|
| 2016 |
Sox7 in tumor endothelial cells promotes VEGFR2 expression and vascular abnormality in high-grade glioma; Sox7 deletion suppressed VEGFR2 expression, while Sox17 deletion exacerbated abnormality by up-regulating Sox7. |
Endothelial conditional deletion, in vivo imaging, immunofluorescence, gene expression analysis |
The Journal of experimental medicine |
High |
29444818
|
| 2017 |
SOX7 directly binds to the VE-cadherin gene promoter and up-regulates its expression in endothelial cells, thereby suppressing endothelial-to-mesenchymal transition (EndMT); luciferase and EMSA confirmed direct promoter binding, and VE-cadherin knockdown partly reverses SOX7-mediated repression of EndMT. |
Luciferase reporter assay, EMSA, collagen gel culture system, VE-cadherin knockdown rescue |
Clinical science |
High |
33720353
|
| 2017 |
Sox7 is expressed in FLK1+ endothelial progenitors and its conditional deletion in FLK1+ cells leads to widespread vascular defects by E10.5 including disorganized endothelial cords instead of paired dorsal aorta; hematopoietic-specific (VAV-cre) deletion of Sox7 does not affect the hematopoietic system. |
FLK1-specific conditional knockout, VAV-specific conditional knockout, histological analysis of embryos from E7.5 to E10.5 |
Mechanisms of development |
High |
28577909
|
| 2017 |
GATA4 specifically regulates Sox7 and Sox18 expression during cardiomyogenesis; knockdown of Gata4 reduces Sox7/Sox18 expression, and reinstating Sox7 or Sox18 partially rescues cardiomyocyte differentiation lost upon Gata4 knockdown; this axis is conserved between Xenopus and mouse ESCs. |
Genome-wide transcriptomics, morpholino knockdown, RNA rescue experiments, mouse ESC knockdown |
Developmental biology |
High |
29229250
|
| 2017 |
SOX7 suppresses Wnt signaling by competing with BCL9 for binding to β-catenin; co-immunoprecipitation showed SOX7 binds β-catenin and disrupts the β-catenin/BCL9 interaction, thereby inhibiting β-catenin/TCF-mediated transcription. |
Co-immunoprecipitation, super TopFlash reporter assay |
DNA and cell biology |
Medium |
29271667
|
| 2017 |
Sox7 regulates Sox7 expression in endothelial cells via ETS factor ETV2; Sox7 is required for endothelial cell VEGFR2 expression, angiogenic sprouting from embryoid bodies, and cardiovascular development. |
Inducible expression, ChIP at Sox7 regulatory region, shRNA knockdown in EBs |
Stem cells and development |
High |
24762086
|
| 2017 |
Sox7 directly represses PSMA/FOLH1 expression by binding to SOX box sites #2 and #4 within the PSMA enhancer (PSME); the nuclear localization signal (NLS) regions of SOX7, but not its β-catenin-interacting motif, are essential for this suppressive activity. |
ChIP, EMSA, luciferase reporter assay, Sox7 NLS mutant, stable expression in prostate cancer cells |
The Prostate |
High |
30488457
|
| 2017 |
SOX7 is identified as a transcriptional repressor of the Hepatitis B virus core promoter (HBVCP); SOX7 binds specifically to the HBVCP via its HMG box and competitively displaces hepatocyte nuclear factor 4α, inhibiting pgRNA synthesis, HBcAg and cccDNA accumulation. |
EMSA, luciferase reporter assay, HBV replicon and infection models, stapled peptide experiments |
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; treatment with proteasome inhibitor MG132/bortezomib or p-ERK/MEK inhibitor U0126 attenuates SOX7-promoted BIM degradation. |
Gene expression profiling, pharmacological inhibition (MG132, bortezomib, U0126), Western blot, loss-of-function |
Oncogene |
Medium |
31332289
|
| 2018 |
SOX7 validated target genes in breast cancer cells include SPRY1 and SLIT2 (SOX7-activated) and TRIB3 and MTHFD2 (SOX7-repressed); these were identified by microarray combined with ChIP validation and confirmed to differentially contribute to tumor suppression. |
Microarray gene expression profiling, ChIP assay, qPCR validation |
International journal of molecular sciences |
Medium |
29757932
|
| 2019 |
SOX7 is required for muscle satellite cell development and maintenance; conditional knockout of Sox7 in PAX3+ cells reduces satellite cell population from birth, reduces myofiber caliber, impairs regeneration after injury, and increases sensitivity to apoptosis; SOX7-deficient primary myoblasts show impaired myoblast fusion. |
Conditional PAX3-Cre knockout mouse, satellite cell quantification, injury-induced regeneration assay, primary myoblast culture |
Stem cell reports |
High |
28943254
|
| 2019 |
Sox7 enforced expression in adult bone marrow progenitors promotes proliferation of multi-lineage short-term engrafting blood progenitors and induces a profound block in B lymphocyte generation both ex vivo and in vivo, causing extra-medullary hematopoiesis in spleen and liver. |
Inducible transgenic mouse model, bone marrow/stroma co-culture, transplantation assay, FACS |
Open biology |
High |
27411892
|
| 2019 |
Sox7 promotes endothelial cell activation via the Jagged1-Notch1 pathway upon HLA I antibody stimulation; Sox7 knockdown reduces adhesion molecules (VCAM-1, ICAM-1), inflammatory cytokines (IL-6, TNF-α), and Jagged1-Notch1 signaling; Jagged1 overexpression rescues the effect of Sox7 knockdown. |
shRNA knockdown, Notch pathway inhibition (DAPT), Jagged1 overexpression rescue, in vivo kidney transplantation model |
Experimental cell research |
Medium |
30639059
|
| 2019 |
Sox7 regulates lineage decisions in cardiovascular progenitor cells by promoting endothelial cell fate at the expense of cardiac lineage; ChIP-Seq combined with ATAC-Seq identified Sox7 target genes; SOX7 directly protein-protein interacts with GATA4 and interferes with GATA4 transcriptional activity on cardiac genes; Sox7 modulates WNT and BMP signaling during cardiovascular differentiation. |
ChIP-Seq, ATAC-Seq, transcriptomics, Co-immunoprecipitation (SOX7-GATA4 interaction), doxycycline-inducible overexpression |
Stem cells and development |
High |
31154937
|
| 2020 |
SOX7 is rapidly and transiently upregulated in human endothelial cells during hypoxia and is required for hypoxia-induced angiogenesis; SOX7 depletion impairs angiogenic response in cultured primary human umbilical vein endothelial cells. |
RNA-Seq temporal profiling, siRNA knockdown, tube formation and sprouting angiogenesis assays |
The Journal of biological chemistry |
Medium |
32071080
|
| 2021 |
Sox7 deficiency in mouse atrioventricular canal reduces Bmp2 in myocardium and Wnt4 in endocardium; Sox7 directly binds to the Wnt4 and Bmp2 promoters; exogenous WNT4 or BMP2 partially rescues impaired endothelial-to-mesenchymal transition (EndMT) caused by Sox7 deficiency, with BMP2 acting downstream of WNT4. |
Conditional knockout mouse, transcriptome analysis, ChIP/direct promoter binding assays, protein rescue experiments, Noggin inhibition |
Cell death & disease |
High |
33846290
|
| 2022 |
Loss-of-function SOX7 mutation (Gln104*) fails to transactivate target genes GATA4 and BMP2 and invalidates cooperative transactivation with NKX2.5, as demonstrated by dual-luciferase reporter analysis; this mutation co-segregates with congenital heart disease in a pedigree. |
Dual-luciferase reporter assay, whole-exome sequencing, Sanger sequencing |
American journal of translational research |
Medium |
35422912
|
| 2023 |
SOX7 in blood vascular endothelial cells non-cell-autonomously patterns lymphatic vessels by directly repressing VEGFC transcription at distant regulatory regions; SOX7 also directly binds HEY1 (a canonical Notch pathway repressor), suggesting recruitment of HEY1 to VEGFC genomic regulatory regions as a mechanism of transcriptional repression. |
Conditional loss-of-function in mice, identification of distant regulatory regions, direct binding assay, Co-IP for SOX7-HEY1 interaction |
The EMBO journal |
High |
36715213
|
| 2023 |
Endothelial-specific loss of Sox7 in mice leads to ventricular non-compaction-like defects and abnormal coronary artery formation; Sox7 loss disrupts transcriptional regulation of Notch pathway genes and connexins 37 and 40, which govern coronary arterial specification; a subset of Sox7-null endothelial cells transdifferentiate into hematopoietic lineages. |
Endothelial-specific conditional knockout, single-nuclei transcriptomics, fate mapping, immunofluorescence |
EMBO reports |
High |
37551717
|
| 2012 |
SOX7 co-localizes with mutant β-catenin or TCF4 in the nucleus and physically interacts with both wild-type and mutant β-catenin as well as TCF4; SOX7 inhibits TCF/LEF-1-dependent transcription induced by Wnt-1 and suppresses Wnt targets Cyclin D1 and c-Myc in endometrial cancer cells. |
Co-immunoprecipitation, immunofluorescent microscopy, luciferase reporter assay, Western blot |
Oncotarget |
High |
23295859
|
| 2024 |
SOX7 binds to the promoter of DNMT3B and transcriptionally represses it, leading to reduced methylation of the CYGB promoter and inhibition of bladder cancer progression; the SOX7/DNMT3B/CYGB axis was validated by ChIP and functional experiments. |
ChIP assay, Western blot, RNA-seq, immunohistochemistry, knockdown and overexpression experiments in BCa cell lines |
Molecular biomedicine |
Medium |
39227479
|