Department of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, 3012 Bern, Switzerland.
Biomolecules. 2020 Apr 16;10(4):614. doi: 10.3390/biom10040614.
Regulatory non-protein coding RNAs perform a remarkable variety of complex biological functions. Previously, we demonstrated a role of the human non-coding vault RNA1-1 (vtRNA1-1) in inhibiting intrinsic and extrinsic apoptosis in several cancer cell lines. Yet on the molecular level, the function of the vtRNA1-1 is still not fully clear. Here, we created HeLa knock-out cell lines revealing that prolonged starvation triggers elevated levels of apoptosis in the absence of vtRNA1-1 but not in vtRNA1-3 knock-out cells. Next-generation deep sequencing of the mRNome identified the PI3K/Akt pathway and the ERK1/2 MAPK cascade, two prominent signaling axes, to be misregulated in the absence of vtRNA1-1 during starvation-mediated cell death conditions. Expression of vtRNA1-1 mutants identified a short stretch of 24 nucleotides of the vtRNA1-1 central domain as being essential for successful maintenance of apoptosis resistance. This study describes a cell signaling-dependent contribution of the human vtRNA1-1 to starvation-induced programmed cell death.
调控性非蛋白编码 RNA 具有多种复杂的生物学功能。此前,我们证明了人类非编码 vault RNA1-1(vtRNA1-1)在几种癌细胞系中抑制内在和外在细胞凋亡的作用。然而,在分子水平上,vtRNA1-1 的功能仍不完全清楚。在这里,我们创建了 HeLa 敲除细胞系,揭示了长期饥饿在没有 vtRNA1-1 的情况下会引发更高水平的细胞凋亡,但在没有 vtRNA1-3 的情况下不会引发细胞凋亡。对 mRNome 的新一代深度测序鉴定了 PI3K/Akt 途径和 ERK1/2 MAPK 级联,这两个突出的信号轴在饥饿介导的细胞死亡条件下 vtRNA1-1 缺失时被错误调节。vtRNA1-1 突变体的表达确定了 vtRNA1-1 中心结构域的 24 个核苷酸短片段对于成功维持抗凋亡至关重要。本研究描述了人类 vtRNA1-1 在饥饿诱导的程序性细胞死亡中依赖细胞信号的作用。