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p53共有结合位点的定义。

Definition of a consensus binding site for p53.

作者信息

el-Deiry W S, Kern S E, Pietenpol J A, Kinzler K W, Vogelstein B

机构信息

Oncology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.

出版信息

Nat Genet. 1992 Apr;1(1):45-9. doi: 10.1038/ng0492-45.

Abstract

Recent experiments have suggested that p53 action may be mediated through its interaction with DNA. We have now identified 18 human genomic clones that bind to p53 in vitro. Precise mapping of the binding sequences within these clones revealed a consensus binding site with a striking internal symmetry, consisting of two copies of the 10 base pair motif 5'-PuPuPuC(A/T)(T/A)GPyPyPy-3' separated by 0-13 base pairs. One copy of the motif was insufficient for binding, and subtle alterations of the motif, even when present in multiple copies, resulted in loss of affinity for p53. Mutants of p53, representing each of the four "hot spots" frequently altered in human cancers, failed to bind to the consensus dimer. These results define the DNA sequence elements with which p53 interacts in vitro and which may be important for p53 action in vivo.

摘要

近期实验表明,p53的作用可能是通过其与DNA的相互作用来介导的。我们现已鉴定出18个人类基因组克隆,它们在体外可与p53结合。对这些克隆内结合序列的精确定位揭示了一个具有显著内部对称性的共有结合位点,该位点由两个10个碱基对基序5'-PuPuPuC(A/T)(T/A)GPyPyPy-3'的拷贝组成,中间间隔0至13个碱基对。该基序的一个拷贝不足以实现结合,并且即使基序存在多个拷贝,其细微改变也会导致对p53亲和力的丧失。代表人类癌症中经常发生改变的四个“热点”的p53突变体无法与共有二聚体结合。这些结果确定了p53在体外与之相互作用且可能对其体内作用很重要的DNA序列元件。

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