Center for Cancer Research, Shantou University Medical College, Shantou, Guangdong, China.
Section of Cell Biology and Genetics, Shantou University Medical College, Shantou, Guangdong, China.
Mol Cell Biochem. 2024 Mar;479(3):653-664. doi: 10.1007/s11010-023-04752-w. Epub 2023 May 8.
Pleckstrin homeolike domain, family A, member 1 (PHLDA1) is a multifunctional protein that plays diverse roles in A variety of biological processes, including cell death, and hence its altered expression has been found in different types of cancer. Although studies have shown a regulatory relationship between p53 and PHLDA1, the molecular mechanism is still unclear. Especially, the role of PHLDA1 in the process of apoptosis is still controversial. In this study, we found that the expression of PHLDA1 in human cervical cancer cell lines was correlated with the up-expression of p53 after treatment with apoptosis-inducing factors. Subsequently, the binding site and the binding effect of p53 on the promoter region of PHLDA1 were verified by our bioinformatics data analysis and luciferase reporter assay. Indeed, we used CRISPR-Cas9 to knockout the p53 gene in HeLa cells and further confirmed that p53 can bind to the promoter region of PHLDA1 gene, and then directly regulate the expression of PHLDA1 by recruiting P300 and CBP to change the acetylation and methylation levels in the promoter region. Finally, a series of gain-of-function experiments further confirmed that p53 re-expression in HeLa cell can up-regulate the reduction of PHLDA1 caused by p53 knockout, and affect cell apoptosis and proliferation. Our study is the first to explore the regulatory mechanism of p53 on PHLDA1 by using the p53 gene knockout cell model, which further proves that PHLDA1 is a target-gene in p53-mediated apoptosis, and reveals the important role of PHLDA1 in cell fate determination.
PLEK 同源结构域家族 A 成员 1(PHLDA1)是一种多功能蛋白,在多种生物过程中发挥着不同的作用,包括细胞死亡,因此在不同类型的癌症中发现其表达发生了改变。虽然研究表明 p53 和 PHLDA1 之间存在调节关系,但分子机制尚不清楚。特别是,PHLDA1 在细胞凋亡过程中的作用仍存在争议。在本研究中,我们发现人宫颈癌细胞系中 PHLDA1 的表达与凋亡诱导因子处理后 p53 的上调表达相关。随后,我们通过生物信息学数据分析和荧光素酶报告基因检测验证了 p53 与 PHLDA1 启动子区域的结合位点和结合效应。确实,我们使用 CRISPR-Cas9 敲除了 HeLa 细胞中的 p53 基因,并进一步证实 p53 可以结合到 PHLDA1 基因的启动子区域,然后通过招募 P300 和 CBP 直接调节 PHLDA1 的表达,改变启动子区域的乙酰化和甲基化水平。最后,一系列功能获得实验进一步证实,p53 在 HeLa 细胞中的重新表达可以上调 p53 敲除导致的 PHLDA1 降低,并影响细胞凋亡和增殖。本研究首次通过使用 p53 基因敲除细胞模型探索了 p53 对 PHLDA1 的调节机制,进一步证明了 PHLDA1 是 p53 介导的凋亡中的靶基因,并揭示了 PHLDA1 在细胞命运决定中的重要作用。