Michel F, Westhof E
Centre de Génétique Moléculaire du CNRS, Laboratoire associé à l'Université Pierre et Marie Curie, Gif-sur-Yvette, France.
J Mol Biol. 1990 Dec 5;216(3):585-610. doi: 10.1016/0022-2836(90)90386-Z.
Alignment of the 87 available sequences of group I self-splicing introns reveals numerous instances of covariation between distant sites. Some of these covariations cannot be ascribed to historical coincidences or the known secondary structure of group I introns, and are, therefore, best explained as reflecting tertiary contacts. With the help of stereochemical modelling, we have taken advantage of these novel interactions to derive a three-dimensional model of the conserved core of group I introns. Two noteworthy features of that model are its extreme compactness and the fact that all of the most evolutionarily conserved residues happen to converge around the two helices that constitute the substrate of the core ribozyme and the site that binds the guanosine cofactor necessary for self-splicing. Specific functional implications are discussed, both with regard to the way the substrate helices are recognized by the core and possible rearrangements of the introns during the self-splicing process. Concerning potential long-range interactions, emphasis is put on the possible recognition of two consecutive purines in the minor groove of a helix by a GAAA or related terminal loop.
对87个可用的I组自我剪接内含子序列进行比对,发现远距离位点之间存在大量共变实例。其中一些共变不能归因于历史巧合或I组内含子已知的二级结构,因此,最好解释为反映三级接触。借助立体化学建模,我们利用这些新的相互作用推导出了I组内含子保守核心的三维模型。该模型的两个显著特征是其极度紧凑,以及所有进化上最保守的残基恰好聚集在构成核心核酶底物的两条螺旋周围,以及自我剪接所需的鸟苷辅因子结合位点周围。文中讨论了具体的功能含义,包括核心如何识别底物螺旋以及自我剪接过程中内含子可能的重排方式。关于潜在的长程相互作用,重点讨论了GAAA或相关末端环在螺旋小沟中对两个连续嘌呤的可能识别。