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首页> 外文期刊>Biochimica et Biophysica Acta. Gene Regulatory Mechanisms >An inhibitory role of p53 via NF-kappaB element on the cyclin D1 gene under heat shock.
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An inhibitory role of p53 via NF-kappaB element on the cyclin D1 gene under heat shock.

机译:在热激条件下,通过NF-κB元件对cyclin D1基因上p53的抑制作用。

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摘要

Little is known about the mechanisms underlying heat shock-mediated inhibition of cyclin D1 transcription. Here, we report that NF-kappaB site-mediated cyclin D1 transcription is inhibited by heat shock. The mRNA level of cyclin D1 decreased under heat shock (40-60%). This inhibition of transcription is promoter activity dependent and is mediated by the proximal NF-kappaB site. However, P65 overexpression did not influence the heat-inducible inhibitory pattern and heat shock did not significantly change the binding activity of p65. P53 can inhibit cyclin D1 promoter activity via an NF-kappaB site-dependent manner and its binding activity increased after heat shock. Importantly, p53 overexpression can prevent cyclin D1 promoter activation by p65. Therefore, we can deduce that p53 inhibits promoter activity under heat shock. These results reveal that the mechanism of heat shock-mediated inhibition of cyclin D1 transcription involves an NF-kappaB site. The data presented provide a new insight into the underlying heat shock inhibition of gene transcription.
机译:关于热激介导的细胞周期蛋白D1转录抑制的机制知之甚少。在这里,我们报告说,NF-κB介导的细胞周期蛋白D1转录受热激抑制。热激下细胞周期蛋白D1的mRNA水平下降(40-60%)。转录的这种抑制依赖于启动子活性,并由近端NF-κB位点介导。但是,P65的过表达不会影响热诱导的抑制模式,并且热休克不会显着改变p65的结合活性。 P53可通过NF-κB位点依赖性方式抑制细胞周期蛋白D1启动子活性,热激后其结合活性增加。重要的是,p53的过度表达可以阻止p65激活细胞周期蛋白D1启动子。因此,我们可以推论p53在热激下抑制启动子活性。这些结果表明,热激介导的细胞周期蛋白D1转录抑制机制涉及NF-κB位点。所提供的数据为潜在的热激抑制基因转录提供了新的见解。

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