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人 vtRNA1-1 水平调节信号通路并调节人癌细胞凋亡。

Human vtRNA1-1 Levels Modulate Signaling Pathways and Regulate Apoptosis in Human Cancer Cells.

机构信息

Department of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.

Graduate School for Cellular and Biomedical Sciences, University of Bern, 3012 Bern, Switzerland.

出版信息

Biomolecules. 2020 Apr 16;10(4):614. doi: 10.3390/biom10040614.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e5/7226377/aa196fb4158f/biomolecules-10-00614-g001.jpg

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