Chechetkin V R, Lobzin V V
Troitsk Institute of Innovation and Thermonuclear Investigations (TRINITI), Theoretical Department of Division for Perspective Investigations, 142190 Troitsk, Moscow Region, Russia.
J Biomol Struct Dyn. 2006 Oct;24(2):189-202. doi: 10.1080/07391102.2006.10507112.
Fourier analysis of the short-range periodicities for the complete set of sequences coding for tRNA genes in genome of Bacillus subtilis proves that periodicities with periods p = 2, 3, 4, and 6 sites are the inherent properties of tRNAs. The related periodicities should be understood in a broad statistical sense and their identifying needs the elaborate statistical methods. To improve the statistics, the analysis of significant periodicities was performed for the binary R-Y, S-W, and K-M sequences. Generally, such short-range periodicities are produced via biased positioning of particular nucleotides rather than via the tandem multiplication and subsequent modifications of repeats, though the latter mechanism may also be realized. Quasi-coherently piercing long segments of tRNA, the short-range periodicities create the effective long-range structural coupling between the acceptor stem and the anticodon loop and may participate in the mechanisms of molecular recognition. The periodicities with p = 2 and 4 provide the natural ground for the translation with spontaneous or programmed frameshifting and are present in tRNAs decoding the most frameshift-prone codons. The observation of short-range periodicities suggests that the mechanisms of amino-acylation of tRNAs and codon-anticodon pairing are not independent. Their study may also provide the important information related to the origin and evolution of the genetic code.
对枯草芽孢杆菌基因组中编码tRNA基因的完整序列集的短程周期性进行傅里叶分析证明,周期为p = 2、3、4和6个位点的周期性是tRNA的固有特性。相关的周期性应从广义的统计学意义上去理解,其识别需要精细的统计方法。为了改进统计,对二元R-Y、S-W和K-M序列进行了显著周期性分析。一般来说,这种短程周期性是通过特定核苷酸的偏向定位产生的,而不是通过串联倍增和随后的重复修饰产生的,尽管后一种机制也可能实现。短程周期性准相干地贯穿tRNA的长片段,在受体茎和反密码子环之间建立有效的长程结构耦合,并可能参与分子识别机制。周期为p = 2和4的周期性为自发或程序性移码翻译提供了天然基础,并且存在于解码最易发生移码的密码子的tRNA中。对短程周期性的观察表明,tRNA的氨基酰化机制和密码子-反密码子配对机制不是独立的。对它们的研究也可能提供与遗传密码的起源和进化相关的重要信息。