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p53对人增殖细胞核抗原启动子的转录激活作用。

Transcriptional activation of the human proliferating-cell nuclear antigen promoter by p53.

作者信息

Morris G F, Bischoff J R, Mathews M B

机构信息

Cold Spring Harbor Laboratory, NY 11724, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):895-9. doi: 10.1073/pnas.93.2.895.

Abstract

Proliferating-cell nuclear antigen (PCNA) is a DNA damage-inducible protein that performs an essential function in DNA replication and repair as an auxiliary factor for DNA polymerases delta and epsilon. Examination of the human PCNA promoter DNA sequence revealed a site with homology to the consensus DNA sequence bound by p53. PCNA promoter fragments with this site intact bound p53 in vitro and were transcriptionally activated by wild-type p53 in transient expression assays in SAOS-2 cells. The resident p53-binding site could be functionally substituted by a previously described p53-binding site from the ribosomal gene cluster. A plasmid expressing a mutated version of p53 derived from a patient with Li-Fraumeni syndrome failed to activate the PCNA promoter in the cotransfection assay. In different cell types, activation of the PCNA promoter by the p53-binding sequence correlated with the status of p53. Activation of the PCNA promoter by wild-type p53 depends upon the level of p53 expression. This concentration dependence and cell type specificity reconciles the observations presented here with prior results indicating that wild-type p53 represses the PCNA promoter. These findings provide a mechanism whereby p53 modulates activation of PCNA expression as a cellular response to DNA damage.

摘要

增殖细胞核抗原(PCNA)是一种DNA损伤诱导蛋白,作为DNA聚合酶δ和ε的辅助因子,在DNA复制和修复中发挥重要作用。对人PCNA启动子DNA序列的研究发现了一个与p53结合的共有DNA序列具有同源性的位点。在体外,含有该完整位点的PCNA启动子片段可结合p53,并且在SAOS-2细胞的瞬时表达试验中,野生型p53可激活其转录。核糖体基因簇中一个先前描述的p53结合位点可在功能上替代该常驻p53结合位点。在共转染试验中,表达来自李-弗劳梅尼综合征患者的p53突变体的质粒无法激活PCNA启动子。在不同细胞类型中,p53结合序列对PCNA启动子的激活与p53的状态相关。野生型p53对PCNA启动子的激活取决于p53的表达水平。这种浓度依赖性和细胞类型特异性将此处的观察结果与先前表明野生型p53抑制PCNA启动子的结果相协调。这些发现提供了一种机制,通过该机制p53可调节PCNA表达的激活,作为细胞对DNA损伤的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b686/40154/337d43a13c13/pnas01506-0361-a.jpg

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