AUTHOR=Biagiotti Sara , Barone Ambra , Aliano Mattia Paolo , Federici Giulia , Malatesta Marco , Caputi Caterina , Soddu Silvia , Leuzzi Vincenzo , Chessa Luciana , Magnani Mauro TITLE=Functional Classification of the ATM Variant c.7157C>A and In Vitro Effects of Dexamethasone JOURNAL=Frontiers in Genetics VOLUME=12 YEAR=2021 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.759467 DOI=10.3389/fgene.2021.759467 ISSN=1664-8021 ABSTRACT=
Most of the ATM variants associated with Ataxia Telangiectasia are still classified as variants with uncertain significance. Ataxia Telangiectasia is a multisystemic disorder characterized by “typical” and “atypical” phenotypes, with early-onset and severe symptoms or with late-onset and mild symptoms, respectively. Here we classified the c.7157C > A ATM variant found in homozygosity in two brothers of Lebanese ethnicity. The brothers presented with an atypical phenotype, showing less than 50% of the positive criteria considered for classification. We performed several in silico analyses to predict the effect of c.7157C > A at the DNA, mRNA and protein levels, revealing that the alteration causes a missense substitution in a highly conserved alpha helix in the FAT domain. 3D structural analyses suggested that the variant might be pathogenic due to either loss of activity or to a structural damage affecting protein stability. Our subsequent