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A novel mechanism of repression of the vascular endothelial growth factor promoter, by single strand DNA binding cold shock domain (Y-box) proteins in normoxic fibroblasts

机译:常氧成纤维细胞中单链DNA结合冷休克域(Y-box)蛋白抑制血管内皮生长因子启动子的新机制

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摘要

Overexpression of vascular endothelial growth factor (VEGF) is implicated in a number of diseases. It is therefore critical that mechanisms exist to strictly regulate VEGF expression. A hypoxia-responsive (HR) region of th VEGF promoter which binds the HIF-1 transcription factor is a target for many signals that up-regulate VEGF transcription. Repressors targeting the HIF-1 transcription factor have been identified but no repressors directly binding the HR promoter region had been reported. We now report a novel mechanism of repression of the VEGF HR region involving DNA binding. We find that single strand DNA-specific cold shock domain (CSD or Y-box) proteins repress the HR region via a binding site downstream of the HIF-1 site. The repressor site is functional in unstimulated, normoxic fibroblasts and represents a novel means to prevent expression of VEGF in the absence of appropriate stimuli. We characterized complexes forming on the VEGF repressor site and identified a previously unreported nuclear CSD protein complex containing dbpA. Nuclear dbpA appears to bind as a dimer and we determined a means by which nuclear CSD proteins may enter double strand DNA to bind to their single strand sites to bring about repression of the VEGF HR region.
机译:血管内皮生长因子(VEGF)的过表达与多种疾病有关。因此,至关重要的是,存在严格调节VEGF表达的机制。与HIF-1转录因子结合的VEGF启动子的低氧应答(HR)区是许多上调VEGF转录的信号的靶标。已经鉴定了靶向HIF-1转录因子的阻遏物,但是没有报道直接结合HR启动子区域的阻遏物。我们现在报告一种新型的机制,抑制涉及DNA结合的VEGF HR区域。我们发现,单链DNA特异的冷激域(CSD或Y-box)蛋白通过HIF-1位点下游的结合位点抑制HR区。阻遏物位点在未受刺激的常氧成纤维细胞中具有功能,并代表一种在没有适当刺激的情况下防止VEGF表达的新手段。我们表征了在VEGF阻遏物位点上形成的复合物,并鉴定了以前未报道的含有dbpA的核CSD蛋白复合物。核dbpA似乎以二聚体的形式结合,我们确定了核CSD蛋白可能进入双链DNA并结合其单链位点以抑制VEGF HR区的方法。

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