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Codon reading scheme in Mycoplasma pneumoniae revealed by the analysis of the complete set of tRNA genes

机译:通过分析完整的tRNA基因揭示肺炎支原体的密码子阅读方案

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The 33 genes encoding the complete set of tRNA species in Mycoplasma pneumoniae have been cloned and sequenced. They are organized into 5 clusters in addition to 9 single genes. No redundant gene was found, indicating that 33 tRNAs correspond to 32 different anticodons and decode all 62 codons used in this organism. There is only one single tRNA for each of theAla, Leu, Pro, and Val family boxes. Therefore, a simplified decoding system resembling that recently described for Mycoplasma capricolum (1) has to also exist in M.pneumoniae. However, analysis of the anticodon set and codon usage revealed features characteristic of the latter: (i) there is no obvious preference toward AT rich synonymous codons, (ii) CGG codons are assigned for arginine and are translated by tRNA Arg(UCG), and (iii) CNN or GNN anticodons are encountered in the Ser, Thr, Arg, and Gly family boxes. We thus propose that this codonanticodon recognition pattern has emerged in the ′M.pneumoniae cluster′ under a genomic economization strategy but without the influence of AT pressure.
机译:已经克隆并测序了编码肺炎支原体中完整tRNA种类的33个基因。除了9个单基因外,它们还分为5个簇。没有发现冗余基因,表明33个tRNA对应于32个不同的反密码子,并解码了该生物体中使用的所有62个密码子。每个Ala,Leu,Pro和Val家族盒只有一个单一的tRNA。因此,在肺炎支原体中也必须存在一种类似于最近针对小支原体(1)描述的简化的解码系统。但是,对反密码子集和密码子使用情况的分析揭示了后者的特征:(i)对于富含AT的同义密码子没有明显的偏好,(ii)为精氨酸分配了CGG密码子,并由tRNA Arg < / sup>(UCG),和(iii)在Ser,Thr,Arg和Gly家族框中遇到CNN或GNN反密码子。因此,我们认为这种密码子识别模式已经在基因组节约策略下出现在“肺炎支原体簇”中,而不受AT压力的影响。

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