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一种激素依赖性tRNA半体通过使p21 mRNA不稳定来促进细胞周期进程。

A hormone-dependent tRNA half promotes cell cycle progression via destabilization of p21 mRNA.

作者信息

Kawamura Takuya, Shigematsu Megumi, Kirino Yohei

机构信息

Computational Medicine Center, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, United States of America.

Department of Biochemistry and Molecular Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, United States of America.

出版信息

PLoS Biol. 2025 Jun 5;23(6):e3003194. doi: 10.1371/journal.pbio.3003194. eCollection 2025 Jun.

Abstract

tRNA halves are among the most abundant short non-coding RNAs in the cellular transcriptome. Here we report that in androgen receptor-positive LNCaP prostate cancer cells, the hormone-dependent 5'-tRNALysCUU half promoted cell proliferation by facilitating cell cycle progression. Global mRNA profiling upon the 5'-tRNALysCUU half depletion revealed that the mRNA of p21, a negative regulator of the cell cycle, is post-transcriptionally destabilized via a 5'-tRNALysCUU half-driven mechanism. YBX1, identified as a protein interacting with 5'-tRNALysCUU half in the cytosol, was shown to stabilize p21 mRNA. Specific sequences resembling the 5'-tRNALysCUU half, located in the 3'-UTR of p21 mRNA and termed LL588, were identified as the binding site for YBX1 and are required for p21 mRNA stability. In vitro binding assays demonstrated that the 5'-tRNALysCUU half is capable of displacing YBX1 from LL588. Collectively, our findings suggest that the 5'-tRNALysCUU half directly binds to and displaces YBX1 from p21 mRNA, leading to the destabilization of p21 mRNA and the promotion of cell cycle progression in hormone-dependent cancers. Our study illuminates the role of tRNA halves in regulating mRNA stability and suggests that this may be part of broader regulatory networks affecting mRNA levels, orchestrated by various tRNA halves and their interacting proteins.

摘要

tRNA半体是细胞转录组中最丰富的短非编码RNA之一。在此我们报告,在雄激素受体阳性的LNCaP前列腺癌细胞中,激素依赖性的5'-tRNALysCUU半体通过促进细胞周期进程来促进细胞增殖。在耗尽5'-tRNALysCUU半体后进行的全基因组mRNA分析显示,细胞周期的负调控因子p21的mRNA通过一种由5'-tRNALysCUU半体驱动的机制在转录后变得不稳定。YBX1被鉴定为一种在细胞质中与5'-tRNALysCUU半体相互作用的蛋白质,它被证明能稳定p21 mRNA。位于p21 mRNA的3'-UTR中、类似于5'-tRNALysCUU半体的特定序列被鉴定为YBX1的结合位点,是p21 mRNA稳定性所必需的。体外结合试验表明,5'-tRNALysCUU半体能够从LL588上取代YBX1。总的来说,我们的研究结果表明,5'-tRNALysCUU半体直接与p21 mRNA结合并从其上取代YBX1,导致p21 mRNA不稳定,并促进激素依赖性癌症中的细胞周期进程。我们的研究阐明了tRNA半体在调节mRNA稳定性中的作用,并表明这可能是影响mRNA水平的更广泛调控网络的一部分,该网络由各种tRNA半体及其相互作用的蛋白质精心编排。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59c5/12140204/e147421c0625/pbio.3003194.g001.jpg

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