Zhang Xin, Trépanier Véronique, Beaujois Remy, Viranaicken Wildriss, Drobetsky Elliot, DesGroseillers Luc
Département de Biochimie et médecine moléculaire, Faculté de médecine, Université de Montréal, 2900 Edouard Montpetit Montréal, QC H3T 1J4, Canada.
Département de Médecine, Université de Montréal and Centre de Recherche, Hôpital Maisonneuve Rosemont, Montréal, Québec, H1T 2M4, Canada.
Nucleic Acids Res. 2016 May 5;44(8):3695-712. doi: 10.1093/nar/gkw057. Epub 2016 Feb 3.
Staufen2 (Stau2) is an RNA-binding protein involved in cell fate decision by controlling several facets of mRNA processing including localization, splicing, translation and stability. Herein we report that exposure to DNA-damaging agents that generate replicative stress such as camptothecin (CPT), 5-fluoro-uracil (5FU) and ultraviolet radiation (UVC) causes downregulation of Stau2 in HCT116 colorectal cancer cells. In contrast, other agents such as doxorubicin and ionizing radiation had no effect on Stau2 expression. Consistently, Stau2 expression is regulated by the ataxia telangiectasia and Rad3-related (ATR) signaling pathway but not by the DNA-PK or ataxia telangiectasia mutated/checkpoint kinase 2 pathways. Stau2 downregulation is initiated at the level of transcription, independently of apoptosis induction. Promoter analysis identified a short 198 bp region which is necessary and sufficient for both basal and CPT-regulated Stau2 expression. The E2F1 transcription factor regulates Stau2 in untreated cells, an effect that is abolished by CPT treatment due to E2F1 displacement from the promoter. Strikingly, Stau2 downregulation enhances levels of DNA damage and promotes apoptosis in CPT-treated cells. Taken together our results suggest that Stau2 is an anti-apoptotic protein that could be involved in DNA replication and/or maintenance of genome integrity and that its expression is regulated by E2F1 via the ATR signaling pathway.
Staufen2(Stau2)是一种RNA结合蛋白,通过控制mRNA加工的多个方面,包括定位、剪接、翻译和稳定性,参与细胞命运的决定。在此我们报告,暴露于产生复制应激的DNA损伤剂,如喜树碱(CPT)、5-氟尿嘧啶(5FU)和紫外线辐射(UVC),会导致HCT116结肠癌细胞中Stau2的下调。相比之下,其他药物如阿霉素和电离辐射对Stau2表达没有影响。一致地,Stau2表达受共济失调毛细血管扩张症和Rad3相关(ATR)信号通路调节,而不受DNA-PK或共济失调毛细血管扩张症突变/检查点激酶2通路调节。Stau2下调在转录水平启动,与凋亡诱导无关。启动子分析确定了一个198 bp的短区域,该区域对于基础和CPT调节的Stau2表达都是必需且充分的。E2F1转录因子在未处理的细胞中调节Stau2,由于CPT处理导致E2F1从启动子上移位,这种作用被消除。引人注目的是,Stau2下调会增加CPT处理细胞中的DNA损伤水平并促进凋亡。综上所述,我们的结果表明Stau2是一种抗凋亡蛋白,可能参与DNA复制和/或基因组完整性的维持,并且其表达受E2F1通过ATR信号通路调节。