Watts George S, Oshiro Marc M, Junk Damian J, Wozniak Ryan J, Watterson Summer, Domann Frederick E, Futscher Bernard W
Bone Marrow Transplant Program, Arizona Cancer Center and Department of Pharmacology and Toxicology, University of Arizona, Tucson, AZ 85724, USA.
Neoplasia. 2004 May-Jun;6(3):187-94. doi: 10.1593/neo.3292.
p300/CBP-associated factor (PCAF) is a coactivator of the tumor suppressor, p53. PCAF participates in p53's transactivation of target genes through acetylation of both bound p53 and histones within p53 target promoters. Using microarrays, we discovered that PCAF itself is induced by p53 in a panel of breast tumor cell lines. Two p53 mutant breast tumor cell lines, BT-549 and UACC-1179, were chosen for further study of PCAF induction by wild-type p53. PCAF induction following adenoviral transduction of p53 expression was confirmed with real-time polymerase chain reaction in a time course experiment. Chromatin immunoprecipitation experiments then showed that PCAF induction was associated with increased p53 binding to the PCAF promoter, which contains p53 consensus-binding sites. PCAF induction by p53 activity was further demonstrated in wild-type p53 MCF10A cells when PCAF expression was induced following activation of endogenous wild-type p53 with doxorubicin in a dose- and time-dependent manner. Furthermore, the doxorubicin-induced increase in PCAF expression was blocked by pretreatment of the MCF10A cells with siRNA (small interfering RNA) targeted against p53 mRNA. Taken together, the results show that PCAF expression can be induced by wild-type p53.
p300/CBP相关因子(PCAF)是肿瘤抑制因子p53的一种共激活因子。PCAF通过对结合的p53以及p53靶基因启动子区域内的组蛋白进行乙酰化修饰,参与p53对靶基因的反式激活作用。利用基因芯片,我们发现在一组乳腺肿瘤细胞系中,PCAF本身可被p53诱导。选取了两株p53突变的乳腺肿瘤细胞系BT - 549和UACC - 1179,用于进一步研究野生型p53对PCAF的诱导作用。在一项时间进程实验中,通过实时聚合酶链反应证实了腺病毒转导p53表达后PCAF的诱导情况。随后的染色质免疫沉淀实验表明,PCAF的诱导与p53与PCAF启动子的结合增加有关,该启动子含有p53的共有结合位点。当用阿霉素以剂量和时间依赖性方式激活内源性野生型p53后诱导PCAF表达时,野生型p53的MCF10A细胞中进一步证明了p53活性对PCAF的诱导作用。此外,用针对p53 mRNA的小干扰RNA(siRNA)预处理MCF10A细胞可阻断阿霉素诱导的PCAF表达增加。综上所述,结果表明PCAF表达可被野生型p53诱导。