Wei Gang, Li Andrew G, Liu Xuan
Department of Biochemistry, University of California, Riverside, California 92521, USA.
J Biol Chem. 2005 Apr 1;280(13):12271-8. doi: 10.1074/jbc.M409522200. Epub 2005 Jan 20.
As a transcription factor, p53 recognizes a specific consensus DNA sequence and activates the expression of the target genes involved in either growth arrest or apoptosis. Despite our wealth of knowledge on the genes that are targeted by p53 in growth arrest and apoptosis, relatively little is known about the promoter specificity triggered by p53 in these processes. Here we show that interaction with c-Abl stabilized p53 tetrameric conformation, and as a consequence c-Abl stimulated p53 DNA binding only when all quarter binding sites (a perfect binding sequence) on p53-responsive promoters were present. This result suggests that in response to DNA damage, c-Abl binding may specifically stimulate p53 DNA binding on the promoters with perfect binding sequences. A sequence comparison of several known p53-responsive elements illustrates the presence of the perfect binding sequences on the p21 but not the Bax promoter. Significantly, we show that c-Abl indeed enhanced p53 DNA binding and transcription from p21 but not Bax. These results suggest that the promoter specificity plays an important role in selective activation of p53 DNA binding by c-Abl. The implications of this with relation to selective activation of p53 target genes involved in either growth arrest or apoptosis are discussed.
作为一种转录因子,p53识别特定的共有DNA序列,并激活参与细胞生长停滞或凋亡的靶基因的表达。尽管我们对p53在细胞生长停滞和凋亡过程中靶向的基因有丰富的了解,但对于p53在这些过程中引发的启动子特异性却知之甚少。在这里,我们表明与c-Abl的相互作用稳定了p53的四聚体构象,因此,只有当p53反应性启动子上的所有四个结合位点(一个完美的结合序列)都存在时,c-Abl才会刺激p53与DNA的结合。这一结果表明,在DNA损伤反应中,c-Abl的结合可能会特异性地刺激p53与具有完美结合序列的启动子上的DNA结合。对几个已知的p53反应元件的序列比较表明,p21启动子上存在完美的结合序列,而Bax启动子上则没有。值得注意的是,我们表明c-Abl确实增强了p53与p21启动子的DNA结合和转录,但对Bax启动子没有影响。这些结果表明,启动子特异性在c-Abl对p53与DNA结合的选择性激活中起着重要作用。我们还讨论了这一结果与p53靶基因在细胞生长停滞或凋亡中的选择性激活之间的关系。