Pinard Robert, Lambert Dominic, Pothiawala Gulnar, Major François, Burke John M
Markey Center for Molecular Genetics, Department of Microbiology and Molecular Genetics, The University of Vermont, Burlington, Vermont 05405, USA.
RNA. 2004 Mar;10(3):395-402. doi: 10.1261/rna.5650904.
Within the hairpin ribozyme, structural elements required for formation of the active tertiary structure are localized in two independently folding domains, each consisting of an internal loop flanked by helical elements. Here, we present results of a systematic examination of the relationship between the structure of the helical elements and the ability of the RNA to form the catalytically active tertiary structure. Deletions and mutational analyses indicate that helix 1 (H1) in domain A can be entirely eliminated, while segments of helices 2, 3, and 4 can also be deleted. From these results, we derive a new active minimal ribozyme that contains three helical elements, an internal loop, and a terminal loop. A three-dimensional model of this truncated ribozyme was generated using MC-SYM, and confirms that the catalytic core of the minimized construct can adopt a tertiary structure that is very similar to that of the nontruncated version. A new strategy is described to study the functional importance of various residues and chemical groups and to identify specific interdomain interactions. This approach uses two physically separated and truncated domains derived from the minimal motif.
在发夹状核酶中,形成活性三级结构所需的结构元件定位于两个独立折叠的结构域中,每个结构域由一个内部环和两侧的螺旋元件组成。在此,我们展示了对螺旋元件结构与RNA形成催化活性三级结构能力之间关系进行系统研究的结果。缺失和突变分析表明,结构域A中的螺旋1(H1)可以完全去除,而螺旋2、3和4的片段也可以被删除。根据这些结果,我们推导得出一种新的活性最小核酶,它包含三个螺旋元件、一个内部环和一个末端环。使用MC-SYM生成了这种截短核酶的三维模型,证实了最小化构建体的催化核心可以采用与未截短版本非常相似的三级结构。描述了一种新策略,用于研究各种残基和化学基团的功能重要性,并识别特定的结构域间相互作用。该方法使用源自最小基序的两个物理上分离且截短的结构域。