Mee T, Okorokov A L, Metcalfe S, Milner J
YCR P53 Research Group, Department of Biology, University of York, UK.
Br J Cancer. 1999 Sep;81(2):212-8. doi: 10.1038/sj.bjc.6690679.
Interaction of p53 with mismatched DNA induces proteolytic cleavage with release of a 35-kDa protein fragment from the p53-DNA complexes. The 35-kDa cleavage product is activated for specific biochemical function(s) and may play a role in the cellular response to DNA damage (Molinari et al (1996) Oncogene 13: 2077-2086; Okorokov et al (1997) EMBO J 16: 6008-6017). In the present study we have asked if mutants of p53 retain the ability to undergo similar proteolytic cleavage, and compared sequence-specific 'DNA contact' with 'structural' mutants commonly found in human cancer. In addition, a series of phosphorylation site mutants were generated to investigate the possible effects of phosphorylation/dephosphorylation on the proteolytic cleavage of p53. All mutants tested bound to a mismatched DNA target in vitro. Moreover, studies in vitro and in vivo indicate that p53 mutants with intact conformational structure (as determined by immunoreactivity with PAb246 and PAb1620) retain the ability to undergo proteolytic cleavage similar, if not identical, to the wild-type p53 protein. Our results suggest that the capacity for p53 to bind mismatched DNA is independent of structural conformation of the central core domain. Proteolytic cleavage, however, is crucially dependent upon a wild-type conformation of the protein.
p53与错配DNA的相互作用会诱导蛋白水解切割,从p53-DNA复合物中释放出一个35 kDa的蛋白片段。这个35 kDa的切割产物被激活以行使特定的生化功能,并且可能在细胞对DNA损伤的反应中发挥作用(Molinari等人,《癌基因》1996年第13卷:2077 - 2086页;Okorokov等人,《欧洲分子生物学组织杂志》1997年第16卷:6008 - 6017页)。在本研究中,我们探究了p53突变体是否保留进行类似蛋白水解切割的能力,并比较了在人类癌症中常见的序列特异性“DNA接触”突变体与“结构”突变体。此外,构建了一系列磷酸化位点突变体,以研究磷酸化/去磷酸化对p53蛋白水解切割的可能影响。所有测试的突变体在体外均能与错配的DNA靶点结合。而且,体外和体内研究表明,具有完整构象结构的p53突变体(通过与PAb246和PAb1620的免疫反应性确定)保留了进行蛋白水解切割的能力,即便与野生型p53蛋白不完全相同,也非常相似。我们的结果表明,p53结合错配DNA的能力与中央核心结构域的结构构象无关。然而,蛋白水解切割关键取决于蛋白的野生型构象。