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Regulation of La/SSB-dependent viral gene expression by pre-tRNA 3′ trailer-derived tRNA fragments

机译:前tRNA 3拖车来源的tRNA片段对La / SSB依赖性病毒基因表达的调控

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摘要

tRNA-derived RNA fragments (tRFs) have emerged as a new class of functional RNAs implicated in cancer, metabolic and neurological disorders, and viral infection. Yet our understanding of their biogenesis and functions remains limited. In the present study, through analysis of small RNA profile we have identified a distinct set of tRFs derived from pre-tRNA 3′ trailers in the hepatocellular carcinoma cell line Huh7. Among those tRFs, tRF_U3_1, which is a 19-nucleotide-long chr10.tRNA2-Ser(TGA)-derived trailer, was expressed most abundantly in both Huh7 and cancerous liver tissues, being present primarily in the cytoplasm. We show that genetic loss of tRF_U3_1 does not affect cell growth and it is not involved in Ago2-mediated gene silencing. Using La/SSB knockout Huh7 cell lines, we demonstrate that this nuclear-cytoplasmic shuttling protein directly binds to the 3′ U-tail of tRF_U3_1 and other abundantly expressed trailers and plays a critical role in their stable cytoplasmic accumulation. The pre-tRNA trailer-derived tRFs capable of sequestering the limiting amounts of La/SSB in the cytoplasm rendered cells resistant to various RNA viruses, which usurp La/SSB with RNA chaperone activity for their gene expression. Collectively, our results establish the trailer-derived tRF-La/SSB interface, regulating viral gene expression.
机译:来自tRNA的RNA片段(tRF)已经作为一类新的功能性RNA出现,涉及癌症,代谢和神经系统疾病以及病毒感染。然而,我们对它们的生物发生和功能的理解仍然有限。在本研究中,通过对小RNA谱的分析,我们在肝细胞癌细胞系Huh7中鉴定出了一组不同的tRF,它们来自于tRNA前3'端。在这些tRF中,tRF_U3_1是长19个核苷酸的chr10.tRNA2-Ser(TGA)衍生的拖车,在Huh7和癌性肝组织中表达最丰富,主要存在于细胞质中。我们表明,tRF_U3_1的遗传损失不会影响细胞生长,并且不参与Ago2介导的基因沉默。使用La / SSB基因敲除Huh7细胞系,我们证明了这种核质穿梭蛋白直接与tRF_U3_1和其他大量表达的拖车的3'U尾结合,并在其稳定的胞质积累中起关键作用。能够隔离细胞质中有限量的La / SSB的tRNA前体来源的tRF能够使细胞对各种RNA病毒具有抗性,从而使具有RNA伴侣活性的La / SSB丧失了基因表达能力。总的来说,我们的结果建立了拖车来源的tRF-La / SSB接口,调节病毒基因的表达。

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