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细菌中异源四聚体甘氨酰-tRNA 合成酶识别 tRNA 的机制。

Mechanism of tRNA recognition by heterotetrameric glycyl-tRNA synthetase from lactic acid bacteria.

机构信息

Department of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, Matsuyama, Ehime 790-8577, Japan.

Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Chiba 277-8562, Japan.

出版信息

J Biochem. 2023 Jul 31;174(3):291-303. doi: 10.1093/jb/mvad043.

Abstract

Glycyl-tRNA synthetases (GlyRSs) have different oligomeric structures depending on the organisms. While a dimeric α2 GlyRS species is present in archaea, eukaryotes and some eubacteria, a heterotetrameric α2β2 GlyRS species is found in most eubacteria. Here, we present the crystal structure of heterotetrameric α2β2 GlyRS, consisting of the full-length α and β subunits, from Lactobacillus plantarum (LpGlyRS), gram-positive lactic bacteria. The α2β2LpGlyRS adopts the same X-shaped structure as the recently reported Escherichia coli α2β2 GlyRS. A tRNA docking model onto LpGlyRS suggests that the α and β subunits of LpGlyRS together recognize the L-shaped tRNA structure. The α and β subunits of LpGlyRS together interact with the 3'-end and the acceptor region of tRNAGly, and the C-terminal domain of the β subunit interacts with the anticodon region of tRNAGly. The biochemical analysis using tRNA variants showed that in addition to the previously defined determinants G1C72 and C2G71 base pairs, C35, C36 and U73 in eubacterial tRNAGly, the identification of bases at positions 4 and 69 in tRNAGly is required for efficient glycylation by LpGlyRS. In this case, the combination of a purine base at Position 4 and a pyrimidine base at Position 69 in tRNAGly is preferred.

摘要

甘氨酰-tRNA 合成酶(GlyRSs)根据生物的不同而具有不同的寡聚体结构。虽然古菌、真核生物和一些原核生物中存在二聚体α2 GlyRS 物种,但大多数原核生物中存在异源四聚体α2β2 GlyRS 物种。在这里,我们展示了来自植物乳杆菌(LpGlyRS)的异源四聚体α2β2 GlyRS 的晶体结构,该结构由全长α和β亚基组成,革兰氏阳性乳酸菌。α2β2LpGlyRS 采用与最近报道的大肠杆菌α2β2 GlyRS 相同的 X 形结构。tRNA 对接模型表明,LpGlyRS 的α和β亚基共同识别 L 形 tRNA 结构。LpGlyRS 的α和β亚基共同与 tRNAGly 的 3'-末端和受体区域相互作用,β亚基的 C 末端结构域与 tRNAGly 的反密码子区域相互作用。使用 tRNA 变体的生化分析表明,除了先前定义的决定因素 G1C72 和 C2G71 碱基对,以及原核生物 tRNAGly 中的 C35、C36 和 U73 之外,tRNAGly 位置 4 和 69 处的碱基的鉴定对于 LpGlyRS 的有效糖基化是必需的。在这种情况下,tRNAGly 中位置 4 的嘌呤碱基和位置 69 的嘧啶碱基的组合是优选的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c37b/10464925/1af3c88ebbe6/mvad043ga.jpg

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