Das Gunajyoti, Lyngdoh R H Duncan
a Department of Chemistry , North-Eastern Hill University , Shillong , 793022 , India .
J Biomol Struct Dyn. 2014;32(9):1500-20. doi: 10.1080/07391102.2013.824822. Epub 2013 Aug 22.
Degeneracy of the genetic code was attributed by Crick to imprecise hydrogen-bonded base-pairing at the wobble position during codon-anticodon pairing. The Crick wobble rules define but do not explain the RNA base pair combinations allowed at this position. We select six pyrimidine bases functioning as anticodon wobble bases (AWBs) to study their H-bonded pairing properties with the four major RNA bases using density functional theory at the B3LYP/6-31G(d,p) level. This is done to assess the extent to which the configuration of a solitary RNA wobble base pair may in itself determine specificity and degeneracy of the genetic code by allowing or disallowing the given base pair during codon-anticodon pairing. Calculated values of select configuration markers for the base pairs screen well between allowed and disallowed base pairs for most cases examined here, where the base pair width emerges as an important factor. A few allowed wobble pairs invoke the involvement of RNA nucleoside conformation, as well as involvement of the exocyclic substituent in H-bonding. This study, however, cannot explain the disallowed status of the Ura⋯Gua wobble pair on the basis of configuration alone. Explanation of the allowed status of the V⋯Ura pair requires further study on the mediatory role of water molecules. Apart from these two cases, these computational results are sufficient, on the basis of base pair configuration alone, to account for the specificity and degeneracy of the genetic code for all known cases of codon-anticodon pairing which involve the pyrimidine AWBs studied here.
遗传密码的简并性被克里克归因于密码子 - 反密码子配对过程中摆动位置处氢键碱基对配对不精确。克里克摆动规则定义了但并未解释该位置允许的RNA碱基对组合。我们选择六个作为反密码子摆动碱基(AWB)的嘧啶碱基,使用B3LYP/6 - 31G(d,p)水平的密度泛函理论研究它们与四种主要RNA碱基的氢键配对特性。这样做是为了评估单个RNA摆动碱基对的构型在密码子 - 反密码子配对过程中通过允许或不允许给定碱基对本身决定遗传密码特异性和简并性的程度。对于此处研究的大多数情况,计算得到的碱基对选择构型标记值能很好地区分允许和不允许的碱基对,其中碱基对宽度是一个重要因素。一些允许的摆动对涉及RNA核苷构象以及环外取代基参与氢键形成。然而,这项研究仅基于构型无法解释尿嘧啶⋯鸟嘌呤摆动对的不允许状态。对V⋯尿嘧啶对允许状态的解释需要进一步研究水分子的介导作用。除了这两种情况,这些计算结果仅基于碱基对构型就足以解释所有已知涉及此处研究的嘧啶AWB的密码子 - 反密码子配对情况下遗传密码的特异性和简并性。