Chanfreau G, Jacquier A
Laboratoire du Métabolisme des ARN (URA 1149 du CNRS), Département des Biotechnologies, Institut Pasteur, Paris, France.
EMBO J. 1996 Jul 1;15(13):3466-76.
As for nuclear pre-mRNA introns, the splicing pathway of group II self-splicing introns proceeds by two successive transesterifications involving substrates with different chemical configurations. These two reactions have been proposed to be catalysed by two active sites, or alternatively by a single active site rearranging its components to accommodate the successive substrates. Here we show that the structural elements specific for the second splicing step are clustered in peripheral structures of domains II and VI. We show that these structures are not required for catalysis of the second chemical step but, instead, take part in a conformational change that occurs between the two catalytic steps. This rearrangement involves the formation of a tertiary contact between part of domain II and a GNRA tetraloop at the tip of domain VI. The fact that domain VI, which carries the branched structure, is involved in this structural rearrangement and the fact that modifications affecting the structures involved have almost no effect when splicing proceeds without branch formation, suggest that the conformational change results in the displacement of the first-step product out of the active site. These observations give further support to the existence of a single active site in group II introns.
至于细胞核前体mRNA内含子,II类自剪接内含子的剪接途径通过两个连续的转酯反应进行,这两个反应涉及具有不同化学构型的底物。有人提出这两个反应由两个活性位点催化,或者由一个单一的活性位点催化,该活性位点重新排列其组分以容纳连续的底物。在这里,我们表明,第二个剪接步骤特有的结构元件聚集在结构域II和VI的外围结构中。我们表明,这些结构对于第二个化学步骤的催化不是必需的,相反,它们参与了两个催化步骤之间发生的构象变化。这种重排涉及结构域II的一部分与结构域VI顶端的GNRA四环之间形成三级接触。携带分支结构的结构域VI参与这种结构重排,以及在没有分支形成的情况下进行剪接时,影响相关结构的修饰几乎没有作用,这一事实表明,构象变化导致第一步产物从活性位点移出。这些观察结果进一步支持了II类内含子中存在单一活性位点的观点。