University of Pittsburgh School of Medicine, Department of Pediatrics, Pittsburgh, PA, United States of America; UPMC Children's Hospital of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA 15224, United States of America.
University of Pittsburgh School of Medicine, Department of Pathology, Pittsburgh, PA. UPMC Children's Hospital of Pittsburgh. 4401 Penn Avenue, Pittsburgh, PA 15224, United States of America.
Mol Genet Metab. 2019 Sep-Oct;128(1-2):1-9. doi: 10.1016/j.ymgme.2019.07.011. Epub 2019 Jul 19.
Inborn errors of metabolism have traditionally been viewed as the quintessential single gene disorders; defects in one gene leads to loss of activity of one enzyme causing a metabolic imbalance and clinical disease. However, reality has never been quite that simple, and the classic "one gene-one enzyme" paradigm has been upended in many ways. Multiple gene defects can lead to the same biochemical phenotype, often with different clinical symptoms. Additionally, different mutations in the same gene can cause variable phenotypes, often most dramatic when a disease can be identified by pre-symptomatic screening. Moreover, response to therapy is not homogeneous across diseases and specific mutations. Perhaps the biggest deviation from traditional monogenic inheritance is in the setting of synergistic heterozygosity, a multigenic inheritance pattern in which mutations in multiple genes in a metabolic pathway lead to sufficient disruption of flux through the pathway, mimicking a monogenic disorder caused by homozygous defects in one gene in that pathway. In addition, widespread adoption of whole exome and whole genome sequencing in medical genetics has led to the realization that individual patients with apparently hybrid phenotypes can have mutations in more than one gene, leading to a mixed genetic disorder. Each of these situations point to a need for as much precision as possible in diagnosing metabolic disease, and it is likely to become increasingly critical to drive therapy. This article examines examples in traditional monogenic disorders that illustrates these points and define inborn errors of metabolism as complex genetic traits on the leading edge of precision medicine.
先天性代谢缺陷传统上被认为是典型的单基因疾病;一个基因的缺陷会导致一种酶的活性丧失,从而导致代谢失衡和临床疾病。然而,现实从未如此简单,经典的“一个基因一个酶”范式在许多方面都被颠覆了。多个基因缺陷可能导致相同的生化表型,通常具有不同的临床症状。此外,同一基因中的不同突变会导致不同的表型,通常在可以通过症状前筛查识别疾病时最为明显。此外,不同疾病的治疗反应并不相同,特定的突变也不相同。也许与传统的单基因遗传最大的偏差是协同性杂合性,这是一种多基因遗传模式,其中代谢途径中多个基因的突变导致通量通过途径充分中断,类似于该途径中纯合缺陷引起的单基因疾病。此外,全外显子组和全基因组测序在医学遗传学中的广泛应用,使得人们认识到,具有明显混合表型的个体患者可能在一个基因中存在多个基因突变,导致混合遗传疾病。这些情况都表明,在诊断代谢疾病时需要尽可能精确,并可能对治疗产生越来越大的影响。本文通过传统单基因疾病的例子来说明这些观点,并将先天性代谢缺陷定义为精准医学前沿的复杂遗传特征。