Toh Zhi Yon Charles, Thandar Aung-Htut May, Pinniger Gavin, Adams Abbie M, Krishnaswarmy Sudarsan, Wong Brenda L, Fletcher Sue, Wilton Steve D
Western Australian Neuroscience Research Institute, Perth, Australia.
University of Western Australia, Perth, Australia.
PLoS One. 2016 Jan 8;11(1):e0145620. doi: 10.1371/journal.pone.0145620. eCollection 2016.
Duchenne and Becker muscular dystrophy severity depends upon the nature and location of the DMD gene lesion and generally correlates with the dystrophin open reading frame. However, there are striking exceptions where an in-frame genomic deletion leads to severe pathology or protein-truncating mutations (nonsense or frame-shifting indels) manifest as mild disease. Exceptions to the dystrophin reading frame rule are usually resolved after molecular diagnosis on muscle RNA. We report a moderate/severe Becker muscular dystrophy patient with an in-frame genomic deletion of DMD exon 5. This mutation has been reported by others as resulting in Duchenne or Intermediate muscular dystrophy, and the loss of this in-frame exon in one patient led to multiple splicing events, including omission of exon 6, that disrupts the open reading frame and is consistent with a severe phenotype. The patient described has a deletion of dystrophin exon 5 that does not compromise recognition of exon 6, and although the deletion does not disrupt the reading frame, his clinical presentation is more severe than would be expected for classical Becker muscular dystrophy. We suggest that the dystrophin isoform lacking the actin-binding sequence encoded by exon 5 is compromised, reflected by the phenotype resulting from induction of this dystrophin isoform in mouse muscle in vivo. Hence, exon skipping to address DMD-causing mutations within DMD exon 5 may not yield an isoform that confers marked clinical benefit. Additional studies will be required to determine whether multi-exon skipping strategies could yield more functional dystrophin isoforms, since some BMD patients with larger in-frame deletions in this region have been reported with mild phenotypes.
杜兴氏和贝克氏肌营养不良症的严重程度取决于DMD基因病变的性质和位置,通常与抗肌萎缩蛋白的开放阅读框相关。然而,存在一些显著的例外情况,即框内基因组缺失会导致严重的病理变化,或者蛋白质截短突变(无义或移码插入/缺失)表现为轻度疾病。抗肌萎缩蛋白阅读框规则的例外情况通常在对肌肉RNA进行分子诊断后得到解决。我们报告了一名中度/重度贝克氏肌营养不良症患者,其DMD基因第5外显子存在框内基因组缺失。其他人曾报道该突变会导致杜兴氏或中间型肌营养不良症,并且一名患者中该框内外显子的缺失导致了多种剪接事件,包括外显子6的缺失,这破坏了开放阅读框并与严重表型一致。所描述的患者缺失了抗肌萎缩蛋白第5外显子,这并未影响外显子6的识别,尽管该缺失并未破坏阅读框,但他的临床表现比经典贝克氏肌营养不良症预期的更为严重。我们认为,缺乏由第5外显子编码的肌动蛋白结合序列的抗肌萎缩蛋白异构体存在缺陷,这在体内小鼠肌肉中诱导该抗肌萎缩蛋白异构体所产生的表型中得到了体现。因此,通过外显子跳跃来解决DMD基因第5外显子内导致疾病的突变可能无法产生具有显著临床益处的异构体。由于已经报道一些该区域存在较大框内缺失的贝克氏肌营养不良症患者具有轻度表型,因此需要进一步的研究来确定多外显子跳跃策略是否能够产生更多功能性的抗肌萎缩蛋白异构体。