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A/T gap tolerance in the core sequence and flanking sequence requirements of non-canonical p53 response elements

机译:非规范p53反应元件核心序列和侧翼序列要求中的A / T缺口耐受性

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摘要

The canonical core sequence of the p53 response element, CATG, has a two-base A/T gap. Previously, we found that p53 can also activate a non-canonical four-base A/T gap CATATG core sequence. In this study, we investigated the possible number of A/T bases used by p53 and showed that a six-base A/T gap CATATATG core sequence was the maximum A/T gap in the p53 response element that could be upregulated by p53 and p63. Canonical and non-canonical p53 response elements also have three-base flanking sequences. A/T bases could be substituted by G/C bases, including CACACG and CGTGTG, but not CGCGCG. We found that the SV40 promoter with functional six- and two-base A/T gap core sequences could be activated by TAp63γ and that TAp63γ could upregulate SV40 small and large T antigens expression in COS7 cells. We also found that the distal region of PUMA promoter with functional two six-base A/T gap core sequences could be activated by TAp63γ in 293T cells. These new findings could provide novel rules for the non-canonical p53 family response element and could extend the entire p53 family regulation network.
机译:p53响应元件的标准核心序列CATG具有两碱基的A / T缺口。以前,我们发现p53还可以激活非规范的四碱基A / T缺口CATATG核心序列。在这项研究中,我们调查了p53使用的A / T碱基的可能数目,并表明六碱基A / T缺口CATATATG核心序列是p53反应元件中的最大A / T缺口,可以通过p53和p53上调。 63规范和非规范p53反应元件也具有三碱基侧翼序列。 A / T基地可以被G / C基地取代,包括CACACG和CGTGTG,但不能由CGCGCG取代。我们发现具有功能性六碱基和两碱基A / T间隙核心序列的SV40启动子可以被TAp63γ激活,并且TAp63γ可以上调COS40细胞中SV40小和大T抗原的表达。我们还发现,具有功能性的两个六碱基A / T间隙核心序列的PUMA启动子的远端区域可以被293T细胞中的TAp63γ激活。这些新发现可能为非规范的p53家族反应元件提供新的规则,并可能扩展整个p53家族调控网络。

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