Hertzog Ashley, Selvanathan Arthavan, Farnsworth Elizabeth, Tchan Michel, Adams Louisa, Lewis Katherine, Tolun Adviye Ayper, Bennetts Bruce, Ho Gladys, Bhattacharya Kaustuv
NSW Biochemical Genetics Service, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, NSW, Australia.
Disciplines of Genetic Medicine and Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Front Genet. 2022 Dec 6;13:1031495. doi: 10.3389/fgene.2022.1031495. eCollection 2022.
Non-coding regions are areas of the genome that do not directly encode protein and were initially thought to be of little biological relevance. However, subsequent identification of pathogenic variants in these regions indicates there are exceptions to this assertion. With the increasing availability of next generation sequencing, variants in non-coding regions are often considered when no causative exonic changes have been identified. There is still a lack of understanding of normal human variation in non-coding areas. As a result, potentially pathogenic non-coding variants are initially classified as variants of uncertain significance or are even overlooked during genomic analysis. In most cases where the phenotype is non-specific, clinical suspicion is not sufficient to warrant further exploration of these changes, partly due to the magnitude of non-coding variants identified. In contrast, inborn errors of metabolism (IEMs) are one group of genetic disorders where there is often high phenotypic specificity. The clinical and biochemical features seen often result in a narrow list of diagnostic possibilities. In this context, there have been numerous cases in which suspicion of a particular IEM led to the discovery of a variant in a non-coding region. We present four patients with IEMs where the molecular aetiology was identified within non-coding regions. Confirmation of the molecular diagnosis is often aided by the clinical and biochemical specificity associated with IEMs. Whilst the clinical severity associated with a non-coding variant can be difficult to predict, obtaining a molecular diagnosis is crucial as it ends diagnostic odysseys and assists in management.
非编码区是基因组中不直接编码蛋白质的区域,最初被认为几乎没有生物学意义。然而,随后在这些区域发现的致病变异表明这一观点存在例外情况。随着下一代测序技术的日益普及,当未发现外显子的致病变化时,通常会考虑非编码区的变异。目前人们对非编码区的正常人类变异仍缺乏了解。因此,潜在的致病性非编码变异最初被归类为意义未明的变异,甚至在基因组分析中被忽视。在大多数表型不特异的情况下,临床怀疑不足以促使对这些变化进行进一步探究,部分原因是所发现的非编码变异数量众多。相比之下,先天性代谢缺陷(IEMs)是一类遗传疾病,其表型特异性通常较高。常见的临床和生化特征往往使诊断可能性的范围较窄。在此背景下,有许多病例是怀疑某种特定的IEM导致了在非编码区发现变异。我们介绍了4例IEM患者,其分子病因在非编码区被确定。IEM相关的临床和生化特异性通常有助于分子诊断的确认。虽然非编码变异相关的临床严重程度可能难以预测,但获得分子诊断至关重要,因为它能结束诊断过程并有助于管理。