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首页> 外文期刊>Cell >Elevated tRNA(iMet) synthesis can drive cell proliferation and oncogenic transformation.
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Elevated tRNA(iMet) synthesis can drive cell proliferation and oncogenic transformation.

机译:升高的tRNA(iMet)合成可以驱动细胞增殖和致癌转化。

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摘要

Characteristics of transformed and tumor cells include increased levels of protein synthesis and elevated expression of RNA polymerase (pol) III products, such as tRNAs and 5S rRNA. However, whether deregulated pol III transcription contributes to transformation has been unclear. Generating cell lines expressing an inducible pol III-specific transcription factor, Brf1, allowed us to raise tRNA and 5S rRNA levels specifically. Brf1 induction caused an increase in cell proliferation and oncogenic transformation, whereas depletion of Brf1 impeded transformation. Among the gene products induced by Brf1 is the tRNA(iMet) that initiates polypeptide synthesis. Overexpression of tRNA(iMet) is sufficient to stimulate cell proliferation and allow immortalized fibroblasts to form foci in culture and tumors in mice. The data indicate that elevated tRNA synthesis can promote cellular transformation.
机译:转化的和肿瘤细胞的特征包括蛋白质合成水平的提高和RNA聚合酶(pol)III产品(例如tRNA和5S rRNA)表达的升高。但是,尚不清楚解除调控的pol III转录是否有助于转化。表达诱导型pol III特异性转录因子Brf1的细胞系的产生,使我们能够特异性提高tRNA和5S rRNA的水平。 Brf1诱导引起细胞增殖和致癌转化的增加,而Brf1的耗竭则阻碍转化。在Brf1诱导的基因产物中,有tRNA(iMet)可以启动多肽合成。 tRNA(iMet)的过度表达足以刺激细胞增殖,并使永生化的成纤维细胞在小鼠的培养物和肿瘤中形成灶。数据表明升高的tRNA合成可以促进细胞转化。

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