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枯草芽孢杆菌 168 菌株中 tRNA 修饰及其对应基因的调查与验证。

Survey and Validation of tRNA Modifications and Their Corresponding Genes in sp Subtilis Strain 168.

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville, FL 32611, USA.

Genetics Institute, University of Florida, Gainesville, FL 32611, USA.

出版信息

Biomolecules. 2020 Jun 30;10(7):977. doi: 10.3390/biom10070977.

Abstract

Extensive knowledge of both the nature and position of tRNA modifications in all cellular tRNAs has been limited to two bacteria, and . sp subtilis strain 168 is the model Gram-positive bacteria and the list of the genes involved in tRNA modifications in this organism is far from complete. Mass spectrometry analysis of bulk tRNA extracted from , combined with next generation sequencing technologies and comparative genomic analyses, led to the identification of 41 tRNA modification genes with associated confidence scores. Many differences were found in this model Gram-positive bacteria when compared to . In general, tRNAs are less modified than those in , even if some modifications, such as mA22 or mstA, are only found in the model Gram-positive bacteria. Many examples of non-orthologous displacements and of variations in the most complex pathways are described. Paralog issues make uncertain direct annotation transfer from to based on homology only without further experimental validation. This difficulty was shown with the identification of the enzyme that introduces ψ at positions 31/32 of the tRNAs. This work presents the most up to date list of tRNA modification genes in , identifies the gaps in knowledge, and lays the foundation for further work to decipher the physiological role of tRNA modifications in this important model organism and other bacteria.

摘要

tRNA 修饰的性质和位置在所有细胞 tRNA 中的广泛知识仅限于两种细菌, 和. 枯草芽孢杆菌 168 株是革兰氏阳性菌模型,该生物体中涉及 tRNA 修饰的基因列表远未完成。从 中提取的 bulk tRNA 的质谱分析,结合下一代测序技术和比较基因组分析,鉴定出 41 个具有相关置信分数的 tRNA 修饰基因。与 相比,在这种模式革兰氏阳性菌中发现了许多差异。一般来说,tRNA 的修饰程度低于 ,即使某些修饰,如 mA22 或 mstA,仅存在于革兰氏阳性菌模型中。描述了许多非同源置换和最复杂途径中的变化的例子。旁系同源问题使得不能仅基于同源性直接从 到 进行注释转移,而无需进一步的实验验证。这一困难在鉴定在 tRNAs 的位置 31/32 处引入 ψ 的 酶时得到了证明。这项工作提供了 中最新的 tRNA 修饰基因列表,确定了知识空白,并为进一步阐明 tRNA 修饰在这个重要的模式生物和其他细菌中的生理作用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5226/7408541/633801b3ea47/biomolecules-10-00977-g001.jpg

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