Fernández A
Department of Chemistry, University of Miami, Coral Gables, FL 33124.
FEBS Lett. 1992 Feb 3;297(1-2):201-4. doi: 10.1016/0014-5793(92)80360-s.
We propose a dynamic model for the competition between exon-exon ligation and 3'-end hydrolysis valid for sequentially folded pre-mRNA introns of group I. This model accounts for the delay in the formation of conserved helix P10 until the 5' exon has been cleaved, a requirement to prevent hydrolysis at the 3' end of the intron. The model is rooted on computer simulations whereby the pre-mRNA searches for its structure as it is being transcribed. Thus, a competing interaction, engaging the internal guiding sequence, occurs initially and prevents P10 from forming until the 3' end of the 5' exon is habilitated as a nucleophilic agent. It is further shown that a destabilization of the competing interaction invariably leads to 3' hydrolysis, crippling the splicing capability of the intron. The results may be probed by site-directed mutagenesis.
我们提出了一个用于外显子-外显子连接与3'端水解之间竞争的动态模型,该模型适用于I组连续折叠的前体mRNA内含子。此模型解释了保守螺旋P10形成的延迟,直到5'外显子被切割,这是防止内含子3'端水解的一个必要条件。该模型基于计算机模拟,即前体mRNA在转录过程中搜索其结构。因此,最初会发生一种涉及内部引导序列的竞争相互作用,阻止P10形成,直到5'外显子的3'端成为亲核试剂。进一步表明,竞争相互作用的不稳定总是导致3'水解,削弱内含子的剪接能力。这些结果可通过定点诱变进行探究。