...
首页> 外文期刊>Biochemical and Biophysical Research Communications >Codon usage revisited: Lack of correlation between codon usage and the number of tRNA genes in enterobacteria
【24h】

Codon usage revisited: Lack of correlation between codon usage and the number of tRNA genes in enterobacteria

机译:密码子用法重新判断:密码子使用与肠杆菌中的TRNA基因数量缺乏相关性

获取原文
获取原文并翻译 | 示例

摘要

It is widely believed that if a high number of genes are found for any tRNA in a rapidly replicating bacteria, then the cytoplasmic levels of that tRNA will be high and an open reading frame containing a higher frequency of the complementary codon will be translated faster. This idea is based on correlations between the number of tRNA genes, tRNA concentration and the frequency of codon usage observed in a limited number of strains as well as from the fact that artificially changing the number of tRNA genes alters translation efficiency and consequently the amount of properly folded protein synthesized. tRNA gene number may greatly vary in a genome due to duplications, deletions and lateral transfer which in turn would alter the levels and functionality of many proteins. Such changes are potentially deleterious for fitness and as a result it is expected that changes in tRNA gene numbers should be accompanied by a modification of the frequency of codon usage. In contrast to this model, when comparing the number of tRNA genes and the frequency of codon usage of several Salmonella enterica and Escherichia coli strains we found that changes in the number of tRNA genes are not correlated to changes in codon usage. Furthermore, these changes are not correlated with a change in the efficiency of codon translation. These results suggest that once a genome gains or loses tRNA genes, it responds by modulating the concentrations of tRNAs rather than modifying its frequency of codon usage. (C) 2018 Elsevier Inc. All rights reserved.
机译:人们普遍认为,如果在快速复制的细菌中发现任何TRNA的基因,那么该TRNA的细胞质水平将高,并且将更快地翻译含有较高互补密码子频率的开放阅读框。该思想基于在有限数量的菌株中观察到的TRNA基因,TRNA浓度和密码子使用频率之间的相关性,以及人工改变TRNA基因的数量改变翻译效率并因此的量合成适当折叠的蛋白质。由于重复,缺失和横向转移,TRNA基因数可能在基因组中大大变化,这反过来会改变许多蛋白质的水平和功能。这种变化对于健身潜在有害,因此预计TRNA基因数的变化应附有密码子使用频率的修改。与该模型相反,当比较TRNA基因的数量和几种沙门氏菌和大肠杆菌菌株的密码子使用的频率时,我们发现TRNA基因数量的变化与密码子使用的变化不相关。此外,这些变化与密码子翻译效率的变化不相关。这些结果表明,一旦基因组增益或失去TRNA基因,它通过调节TRNA的浓度而不是改变其密码子使用的频率来响应。 (c)2018年Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号