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Increased Affinity for RNA Targets Evolved Early in Animal and Plant Dicer Lineages through Different Structural Mechanisms

机译:通过不同的结构机制,在动植物切丁谱系中早期进化出对RNA靶标的亲和力增加

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摘要

Understanding the structural basis for evolutionary changes in protein function is central to molecular evolutionary biology and can help determine the extent to which functional convergence occurs through similar or different structural mechanisms. Here, we combine ancestral sequence reconstruction with functional characterization and structural modeling to directly examine the evolution of sequence-structure-function across the early differentiation of animal and plant Dicer/DCL proteins, which perform the first molecular step in RNA interference by identifying target RNAs and processing them into short interfering products. We found that ancestral Dicer/DCL proteins evolved similar increases in RNA target affinities as they diverged independently in animal and plant lineages. In both cases, increases in RNA target affinities were associated with sequence changes that anchored the RNA’s 5′phosphate, but the structural bases for 5′phosphate recognition were different in animal versus plant lineages. These results highlight how molecular-functional evolutionary convergence can derive from the evolution of unique protein structures implementing similar biochemical mechanisms.
机译:了解蛋白质功能进化变化的结构基础是分子进化生物学的核心,可以帮助确定通过相似或不同的结构机制发生功能趋同的程度。在这里,我们将祖先序列重建与功能表征和结构建模相结合,直接检查动植物Dicer/DCL蛋白早期分化过程中序列-结构-功能的演变,这些蛋白通过识别靶RNA并将其加工成短干扰产物来执行RNA干扰的第一个分子步骤。我们发现,祖先的Dicer / DCL蛋白在动物和植物谱系中独立分化时,进化出类似的RNA靶标亲和力增加。在这两种情况下,RNA靶标亲和力的增加都与锚定RNA的5'磷酸盐的序列变化有关,但5'磷酸盐识别的结构基础在动物和植物谱系中是不同的。这些结果强调了分子功能进化趋同如何从实现类似生化机制的独特蛋白质结构的进化中得出。

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