首页> 美国卫生研究院文献>Biochemical Journal >Effects of nucleotide substitutions within the T-loop of precursor tRNAs on interaction with ATP/CTP:tRNA nucleotidyltransferases from Escherichia coli and yeast.
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Effects of nucleotide substitutions within the T-loop of precursor tRNAs on interaction with ATP/CTP:tRNA nucleotidyltransferases from Escherichia coli and yeast.

机译:前体tRNA的T环内核苷酸取代对与大肠杆菌和酵母中ATP / CTP:tRNA核苷酸转移酶相互作用的影响。

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摘要

Recognition of tRNA and tRNA-like substrates by the enzyme ATP/CTP:tRNA nucleotidyltransferase requires chemically intact nucleotides within the T-loop, especially at positions 57 and 58, which are invariant purines among naturally occurring tRNAs. To test the effects of base substitutions at these positions, which are distant from the site of catalysis, we synthesized mutant tRNA(Glu) molecules. These in vitro-synthesized RNAs also contained an extra 33 bases at the 5' end and lacked post-transcriptionally modified bases. The precursor tRNAs were used as substrates for nucleotidyltransferases from Escherichia coli and yeast. Substitution of cytidines at either position 57 or 58 had dramatic inhibitory effects on recognition by both enzymes, including raising the apparent Km and lowering the apparent Vmax.; substitution of an adenosine at position 57 or a uridine at position 58 inhibited the reaction only slightly by comparison. Our results demonstrate that the identities of nucleotides at positions 57 and 58 are relevant to recognition by nucleotidyltransferase, and that a purine is required at position 57. The extra bases at the 5' end and the lack of post-transcriptionally modified bases did not substantially inhibit interaction with the enzyme, as judged by the wild-type precursor tRNA(Glu) acting as an effective substrate for both enzymes in the presence of equal concentrations of appropriate tRNA substrates isolated from E. coli.
机译:ATP / CTP:tRNA核苷酸转移酶对tRNA和类似tRNA的底物的识别需要T环内的化学上完整的核苷酸,特别是在位置57和58上,它们是天然tRNA中不变的嘌呤。为了测试碱基取代在远离催化位点的这些位置的作用,我们合成了突变的tRNA(Glu)分子。这些体外合成的RNA在5'末端还包含33个碱基,并且缺少转录后修饰的碱基。前体tRNA用作大肠杆菌和酵母中核苷酸基转移酶的底物。在57或58位的胞苷取代对两种酶的识别都具有显着的抑制作用,包括提高表观Km和降低表观Vmax。通过比较,在57位的腺苷或58位的尿苷的取代仅轻微抑制了反应。我们的结果表明,第57和58位核苷酸的身份与核苷酸转移酶的识别有关,并且第57位需要嘌呤。5'端的额外碱基和缺少转录后修饰的碱基基本上没有在存在相同浓度的从大肠杆菌中分离的合适tRNA底物的情况下,野生型前体tRNA(Glu)充当了两种酶的有效底物,从而抑制了与酶的相互作用。

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