Laboratory of Genetics and Genomics, National Institute on Aging (NIA) Intramural Research Program (IRP), National Institutes of Health (NIH), Baltimore, MD, USA.
Regulatory RNAs and Cancer Section, Genetics Branch, Center for Cancer Research, National Cancer Institute IRP, NIH, Bethesda, MD, USA.
Nucleic Acids Res. 2021 Feb 22;49(3):1631-1646. doi: 10.1093/nar/gkaa1246.
Mammalian circRNAs can influence different cellular processes by interacting with proteins and other nucleic acids. Here, we used ribonucleoprotein immunoprecipitation (RIP) analysis to identify systematically the circRNAs associated with the cancer-related protein AUF1. Among the circRNAs interacting with AUF1 in HeLa (human cervical carcinoma) cells, we focused on hsa_circ_0032434 (circPCNX), an abundant target of AUF1. Overexpression of circPCNX specifically interfered with the binding of AUF1 to p21 (CDKN1A) mRNA, thereby promoting p21 mRNA stability and elevating the production of p21, a major inhibitor of cell proliferation. Conversely, silencing circPCNX increased AUF1 binding to p21 mRNA, reducing p21 production and promoting cell division. Importantly, eliminating the AUF1-binding region of circPCNX abrogated the rise in p21 levels and rescued proliferation. Therefore, we propose that the interaction of circPCNX with AUF1 selectively prevents AUF1 binding to p21 mRNA, leading to enhanced p21 mRNA stability and p21 protein production, thereby suppressing cell growth.
哺乳动物 circRNAs 可以通过与蛋白质和其他核酸相互作用来影响不同的细胞过程。在这里,我们使用核糖核蛋白免疫沉淀(RIP)分析系统地鉴定与癌症相关蛋白 AUF1 相关的 circRNAs。在 HeLa(人宫颈癌)细胞中与 AUF1 相互作用的 circRNAs 中,我们重点关注 hsa_circ_0032434(circPCNX),这是 AUF1 的一个丰富靶点。circPCNX 的过表达特异性干扰 AUF1 与 p21(CDKN1A)mRNA 的结合,从而促进 p21 mRNA 的稳定性,并提高 p21 的产生,p21 是细胞增殖的主要抑制剂。相反,沉默 circPCNX 增加了 AUF1 与 p21 mRNA 的结合,减少了 p21 的产生并促进了细胞分裂。重要的是,消除 circPCNX 的 AUF1 结合区消除了 p21 水平的升高并挽救了增殖。因此,我们提出 circPCNX 与 AUF1 的相互作用选择性地阻止 AUF1 与 p21 mRNA 结合,导致 p21 mRNA 稳定性增强和 p21 蛋白产生增加,从而抑制细胞生长。