Biochemistry. 2019 Apr 16;58(15):2061-2076. doi: 10.1021/acs.biochem.9b00062. Epub 2019 Apr 1.
Duchenne muscular dystrophy (DMD) is a common and devastating genetic disease primarily caused by exon deletions that create a genetic frameshift in dystrophin. Exon skipping therapy seeks to correct this by masking an exon during the mRNA maturation process, restoring dystrophin expression, but creating an edited protein missing both the original defect and the therapeutically skipped region. Crucially, it is possible to correct many defects in alternative ways, by skipping an exon either before or after the patient's defect. This results in alternatively edited, hybrid proteins that might have different properties and therapeutic consequences. We examined three such dystrophin exon-skipped edits, Δe45-53, Δe46-54, and Δe47-55, comprising two pairs of alternative repairs of Δe46-53 and Δe47-54 DMD defects. We found that in both cases, Δe46-54 was the more stable repair as determined by a variety of thermodynamic and biochemical measurements. We also examined the origin of these differences with molecular dynamics simulations, which showed that these stability differences were the result of different types of structural perturbations. For example, in one edit there was partial unfolding at the edit site that caused domain-localized perturbations while in another there was unfolding at the protein domain junctions distal to the edit site that increased molecular flexibility. These results demonstrate that alternative exon skip repairs of the same underlying defect can have very different consequences at the level of protein structure and stability and furthermore that these can arise by different mechanisms, either locally or by more subtle long-range perturbations.
杜氏肌营养不良症(DMD)是一种常见且严重的遗传性疾病,主要由外显子缺失引起,导致肌营养不良蛋白发生遗传移码。外显子跳跃疗法试图通过在 mRNA 成熟过程中掩盖外显子来纠正这种情况,从而恢复肌营养不良蛋白的表达,但会产生一种编辑后的蛋白,既缺失原始缺陷,又缺失治疗性跳跃区域。至关重要的是,通过在患者缺陷之前或之后跳过外显子,可以以多种替代方式纠正许多缺陷。这会产生具有不同性质和治疗后果的替代性编辑的混合蛋白。我们研究了三种肌营养不良蛋白外显子跳跃编辑,Δe45-53、Δe46-54 和 Δe47-55,它们包含对 Δe46-53 和 Δe47-54 DMD 缺陷的两种替代性修复的两对。我们发现,通过各种热力学和生化测量,在这两种情况下,Δe46-54 都是更稳定的修复。我们还通过分子动力学模拟研究了这些差异的起源,结果表明这些稳定性差异是由于不同类型的结构扰动造成的。例如,在一种编辑中,编辑部位发生部分展开,导致结构域局部扰动,而在另一种编辑中,编辑部位远端的蛋白质结构域连接处发生展开,增加了分子的灵活性。这些结果表明,同一潜在缺陷的替代性外显子跳跃修复在蛋白质结构和稳定性水平上可能具有非常不同的后果,并且这些后果可能是由不同的机制引起的,要么是局部的,要么是更微妙的远程扰动。