Key Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University, Nanjing, 210096, China.
Jiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, 210009, China.
Cell Death Differ. 2023 Mar;30(3):779-793. doi: 10.1038/s41418-022-01085-x. Epub 2022 Nov 12.
Activation of the pro-apoptotic genes by the p53 family is a critical step in induction of apoptosis. However, the molecular signaling underlying their suppression remains largely unknown. Here, we report a general role of QSER1 in preventing apoptosis. QSER1 is widely up-regulated in multiple cancers, and its up-regulation correlates with poor clinic outcomes. QSER1 knockdown significantly promotes apoptosis in both p53 wild type and mutant cancer cells. Interestingly, we show that QSER1 and p53 occupy distinct cis-regulatory regions in a common subset of the pro-apoptotic genes, and function antagonistically to maintain their proper expression. Furthermore, we identify a key regulatory DNA element named QSER1 binding site in PUMA (QBP). Deletion of QBP de-represses PUMA and induces apoptosis. Mechanistically, QSER1 functions together with SIN3A to suppress PUMA in a p53-dependent and -independent manner, suggesting that QSER1 inhibition might be a potential therapeutic strategy to induce apoptosis in cancers.
p53 家族对促凋亡基因的激活是诱导细胞凋亡的关键步骤。然而,其抑制的分子信号通路在很大程度上仍是未知的。在这里,我们报道了 QSER1 在防止细胞凋亡中的一般作用。QSER1 在多种癌症中广泛上调,其上调与不良的临床结局相关。QSER1 的敲低显著促进 p53 野生型和突变型癌细胞的凋亡。有趣的是,我们表明 QSER1 和 p53 占据了促凋亡基因中常见亚群的不同顺式调控区,并以拮抗的方式发挥作用,以维持其适当的表达。此外,我们在 PUMA(QBP)中鉴定了一个名为 QSER1 结合位点的关键调节 DNA 元件。QBP 的缺失可解除对 PUMA 的抑制并诱导细胞凋亡。从机制上讲,QSER1 与 SIN3A 一起在 p53 依赖和非依赖的方式下抑制 PUMA,这表明抑制 QSER1 可能是诱导癌症细胞凋亡的一种潜在治疗策略。