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细胞四氢生物蝶呤水平的改变可能在小鼠红白血病细胞分化过程中调节tRNA的喹啉低修饰。

Alterations in cell tetrahydrobiopterin levels may regulate queuine hypomodification of tRNA during differentiation of murine erythroleukemia cells.

作者信息

Parniak M A, Andrejchyshyn S, Marx S, Kleiman L

机构信息

Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, Montreal, Quebec, Canada.

出版信息

Exp Cell Res. 1991 Jul;195(1):114-8. doi: 10.1016/0014-4827(91)90506-p.

Abstract

The base at the first anticodon ("wobble") position of certain eukaryotic tRNA species is either guanine or the hypermodified base queuine. These tRNA species are synthesized with guanine in the wobble position (tRNAG); this guanine can then be replaced with queuine by the action of the enzyme tRNA-guanine ribosyltransferase. In the present report, we show that tRNAG levels increased in response to the induction of erythroid differentiation of murine erythroleukemia (MEL) cells. We also found that tRNA-guanine ribosyltransferase was significantly inhibited by tetrahydrobiopterin. MEL cells showed a transient threefold increase in tetrahydrobiopterin levels 6 to 12 h after exposure of the cells to inducers such as DMSO or tetramethylurea. The increase in tetrahydrobiopterin preceded the increase in tRNAG which in turn preceded the appearance of phenotypic changes characteristic of differentiation. By contrast, a mutant MEL cell line unable to differentiate in response to inducers showed no change in the level of tetrahydrobiopterin or of tRNAG upon exposure to DMSO. N-acetylserotonin, a well-characterized inhibitor of tetrahydrobiopterin synthesis, prevented the DMSO-mediated increase in tetrahydrobiopterin in normal MEL cells. N-acetylserotonin also inhibited the increase in tRNAG levels and the appearance of phenotypic differentiation in these cells.

摘要

某些真核生物tRNA种类在第一个反密码子(“摆动”)位置的碱基要么是鸟嘌呤,要么是高度修饰的碱基queuine。这些tRNA种类在摆动位置合成时带有鸟嘌呤(tRNAG);然后,通过tRNA-鸟嘌呤核糖基转移酶的作用,这个鸟嘌呤可以被queuine取代。在本报告中,我们表明,响应小鼠红白血病(MEL)细胞红系分化的诱导,tRNAG水平升高。我们还发现,四氢生物蝶呤可显著抑制tRNA-鸟嘌呤核糖基转移酶。将MEL细胞暴露于二甲基亚砜(DMSO)或四甲基脲等诱导剂后6至12小时,四氢生物蝶呤水平出现短暂的三倍增加。四氢生物蝶呤的增加先于tRNAG的增加,而tRNAG的增加又先于分化特征性表型变化的出现。相比之下,一个不能对诱导剂作出分化反应的突变MEL细胞系,在暴露于DMSO后,四氢生物蝶呤或tRNAG水平没有变化。N-乙酰血清素是一种已被充分表征的四氢生物蝶呤合成抑制剂,可阻止正常MEL细胞中DMSO介导的四氢生物蝶呤增加。N-乙酰血清素还抑制这些细胞中tRNAG水平的增加和表型分化的出现。

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