Departamento de Bioquímica, Biología Molecular y Celular, Universidad de Zaragoza, 50009 and 50013, Zaragoza, Spain.
Instituto de Investigación Sanitaria (IIS) de Aragón, 50009, Zaragoza, Spain.
Orphanet J Rare Dis. 2022 Aug 19;17(1):316. doi: 10.1186/s13023-022-02428-0.
Population frequency has been one of the most widely used criteria to help assign pathogenicity to newly described mitochondrial DNA variants. However, after sequencing this molecule in thousands of healthy individuals, it has been observed that a very large number of genetic variants have a very low population frequency, which has raised doubts about the utility of this criterion. By analyzing the genetic variation of mitochondrial DNA-encoded genes for oxidative phosphorylation subunits in 195,983 individuals from HelixMTdb that were not sequenced based on any medical phenotype, we show that rare variants are deleterious and, along with other criteria, population frequency is still a useful criterion to assign pathogenicity to newly described variants.
人群频率一直是用于帮助将新描述的线粒体 DNA 变体致病性分类的最广泛使用的标准之一。然而,在对数以千计的健康个体进行该分子测序后,人们观察到大量遗传变体的人群频率非常低,这引发了对该标准实用性的质疑。通过分析 HelixMTdb 中 195983 名未基于任何医学表型进行测序的个体中线粒体 DNA 编码氧化磷酸化亚基的基因的遗传变异,我们表明罕见变体是有害的,并且与其他标准一起,人群频率仍然是将新描述的变体致病性分类的有用标准。