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野生型p53对基础c-fos启动子的抑制作用。

Repression of the basal c-fos promoter by wild-type p53.

作者信息

Kley N, Chung R Y, Fay S, Loeffler J P, Seizinger B R

机构信息

Molecular Neuro-Oncology Laboratory, Massachusetts General Hospital, Charlestown.

出版信息

Nucleic Acids Res. 1992 Aug 11;20(15):4083-7. doi: 10.1093/nar/20.15.4083.

Abstract

Mutations in the p53 gene are the most common genetic alterations observed in many inherited and sporadic forms of human cancer. Recent studies indicate that wild-type p53 may be involved in the regulation of gene expression. In the present report we examined the effect of p53 on the human c-fos promoter. Using a transient co-transfection assay we show that wild-type human p53, but not a transforming mutant of p53, negatively regulates the activity of the c-fos promoter in a dose-dependent manner. Promoter deletion analysis maps a sequence conferring p53 repression to the basal promoter region between nucleotides -53 and +42 relative to the cap site. In contrast, p53 strongly stimulates transcription when a sequence previously reported to bind p53 (TGCCT repeat) was inserted in front of the HSV-TK promoter driving CAT. These findings raise the question as to whether p53 may mediate its inhibitory effect on c-fos gene expression by interfering, directly or indirectly, with components of the basal transcriptional machinery.

摘要

p53基因的突变是在许多遗传性和散发性人类癌症中观察到的最常见的基因改变。最近的研究表明,野生型p53可能参与基因表达的调控。在本报告中,我们研究了p53对人c-fos启动子的影响。使用瞬时共转染实验,我们发现野生型人p53,而不是p53的转化突变体,以剂量依赖的方式负向调节c-fos启动子的活性。启动子缺失分析将赋予p53抑制作用的序列定位到相对于帽位点的核苷酸-53至+42之间的基础启动子区域。相反,当一个先前报道的与p53结合的序列(TGCCT重复序列)插入到驱动CAT的HSV-TK启动子之前时,p53强烈刺激转录。这些发现提出了一个问题,即p53是否可能通过直接或间接干扰基础转录机制的成分来介导其对c-fos基因表达的抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57f2/334091/ef4b0465f654/nar00226-0268-a.jpg

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