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大肠杆菌中tRNA-鸟嘌呤转糖基酶对tRNA的识别:U33在U-G-U序列识别中的作用

tRNA recognition by tRNA-guanine transglycosylase from Escherichia coli: the role of U33 in U-G-U sequence recognition.

作者信息

Nonekowski S T, Garcia G A

机构信息

Interdepartmental Program in Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor 48109-1065, USA.

出版信息

RNA. 2001 Oct;7(10):1432-41.

Abstract

In eubacteria, the biosynthesis of queuine, a modified base found in the wobble position (#34) of tRNAs coding for Tyr, His, Asp, and Asn, occurs via a multistep pathway. One of the key enzymes in this pathway, tRNA-guanine transglycosylase (TGT), exchanges the genetically encoded guanine at position 34 with a queuine precursor, preQ1. Previous studies have identified a minimal positive RNA recognition motif for Escherichia coli TGT consisting of a stable minihelix that contains a U-G-U sequence starting at the second position of its seven base anticodon loop. Recently, we reported that TGT was capable of recognizing the U-G-U sequence outside of this limited structural context. To further characterize the ability of TGT to recognize the U-G-U sequence in alternate contexts, we constructed mutants of the previously characterized E. coli tRNA(Tyr) minihelix. The U-G-U sequence was shifted to various positions within the anticodon loop of these mutants. Characterization of these analogs demonstrates that in addition to the normal U33G34U35 position, TGT can also recognize the U34G35U36 analog (UGU(+1)). The other analogs were not active. This indicates that the recognition of the U-G-U sequence is not strictly dependent upon its position relative to the stem. In E. coli, the full-length tRNA with a U34G35U36 anticodon sequence is one of the isoacceptors that codes for threonine. We found that TGT is able to recognize tRNA(Thr(UGU)) but only in the absence of a uridine at position 33. U33, an invariant base present in all tRNAs, has been shown to strongly influence the conformation of the anticodon loop of certain tRNAs. We find that mutation of this base confers on TGT the ability to recognize U34G35U36, and suggests that loop conformation affects recognition. The fact that the other analogs were not active indicates that although TGT is capable of recognizing the U-G-U sequence in additional contexts, this recognition is not indiscriminate.

摘要

在真细菌中,反密码子位置(#34)上存在修饰碱基 queuine 的 tRNA 编码 Tyr、His、Asp 和 Asn,其生物合成通过多步途径进行。该途径中的关键酶之一,tRNA-鸟嘌呤转糖基酶(TGT),将第 34 位的基因编码鸟嘌呤与 queuine 前体 preQ1 进行交换。先前的研究已经确定了大肠杆菌 TGT 的一个最小正向 RNA 识别基序,它由一个稳定的小螺旋组成,该小螺旋在其七个碱基的反密码子环的第二个位置起始处包含一个 U-G-U 序列。最近,我们报道 TGT 能够在这个有限的结构背景之外识别 U-G-U 序列。为了进一步表征 TGT 在不同背景下识别 U-G-U 序列的能力,我们构建了先前表征的大肠杆菌 tRNA(Tyr)小螺旋的突变体。U-G-U 序列在这些突变体的反密码子环内移动到了不同位置。对这些类似物的表征表明,除了正常的 U33G34U35 位置外,TGT 还能识别 U34G35U36 类似物(UGU(+1))。其他类似物没有活性。这表明对 U-G-U 序列的识别并不严格依赖于其相对于茎的位置。在大肠杆菌中,具有 U34G35U36 反密码子序列的全长 tRNA 是编码苏氨酸的同工受体之一。我们发现 TGT 能够识别 tRNA(Thr(UGU)),但仅在第 33 位没有尿苷的情况下。U33 是所有 tRNA 中都存在的一个不变碱基,已被证明会强烈影响某些 tRNA 的反密码子环的构象。我们发现该碱基的突变赋予了 TGT 识别 U34G35U36 的能力,并表明环构象会影响识别。其他类似物没有活性这一事实表明,尽管 TGT 能够在其他背景下识别 U-G-U 序列,但这种识别并非不加选择的。

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