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Identification of factors that promote biogenesis of tRNA(CGA)(Ser)

机译:鉴定促进TRNA生物发生(CGA)(SER)的因素

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摘要

A wide variety of factors are required for the conversion of pre-tRNA molecules into the mature tRNAs that function in translation. To identify factors influencing tRNA biogenesis, we previously performed a screen for strains carrying mutations that induce lethality when combined with a sup61-T47:2C allele, encoding a mutant form of Analyzes of two complementation groups led to the identification of Tan1 as a protein involved in formation of the modified nucleoside N-4-acetylcytidine (ac(4)C) in tRNA and Bud13 as a factor controlling the levels of ac(4)C by promoting TAN1 pre-mRNA splicing. Here, we describe the remaining complementation groups and show that they include strains with mutations in genes for known tRNA biogenesis factors that modify (DUS2, MOD5 and TRM1), transport (LOS1), or aminoacylate (SES1) Other strains carried mutations in genes for factors involved in rRNA/mRNA synthesis (RPA49, RRN3 and MOT1) or magnesium uptake (ALR1). We show that mutations in not only DUS2, LOS1 and SES1 but also in RPA49, RRN3 and MOT1 cause a reduction in the levels of the altered These results indicate that Rpa49, Rrn3 and Mot1 directly or indirectly influence biogenesis.
机译:将预流量转化为在翻译中的成熟TrNA中,需要各种各样的因素。为了鉴定影响TRNA生物发生的因素,我们之前对携带诱导致死性的诱导筛选诱导致死性的筛选,所述诱导致死性与Sup61-T47:2C等位基因组合,编码两个互补基团的突变形式的分析导致Tan1作为所涉及的蛋白质的鉴定在TRNA和BUS13中形成改性核苷N-4-乙酰胞嘧啶(AC(4)C)作为通过促进TAN1预-mRNA剪接来控制AC(4)C水平的因子。在这里,我们描述了剩余的互补组,并表明它们包括用于修饰(DUS2,MOD5和TRM1),运输(LOS1)或氨基酰化物(SES1)其他菌株在基因中进行突变的已知的TRNA生物发生因子中具有基因突变的菌株。参与RRNA / mRNA合成的因素(RPA49,RRN3和MOT1)或镁摄取(AL1)。我们表明,不仅在RPA49,RRN3和MOT1中的突变也不仅在RPA49,RRN3和MOT1也会导致这些结果的改变水平的降低表明RPA49,RRN3和MOT1直接或间接地影响生物发生。

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