Functional Characterization of Thyroid Peroxidase Missense Variants Causing Thyroid Dyshormonogenesis in Asian Indian Population

Abstract

<b><i>Introduction:</i></b> Thyroid dyshormonogenesis (TDH) is a subgroup of congenital hypothyroidism with recessive inheritance resulting from disease-causing variants in thyroid hormone biosynthesis pathway genes, like <i>DUOX2</i>, <i>TG</i>, <i>TPO</i>, <i>SLC5A5</i>, <i>SLC26A4</i>, <i>IYD</i>, <i>DUOXA2</i>, and <i>SLC26A7</i>. Thyroid peroxidase (TPO) is a crucial enzyme involved in thyroid hormone biosynthesis and is one of the frequently mutated genes in patients with TDH. The purpose of the study was to describe the in silico and functional characterization of novel variants in <i>TPO</i> gene identified in patients with TDH. <b><i>Methods:</i></b> We performed exome sequencing in Indian patients with TDH. In the current study, we describe the results of patients with <i>TPO</i> gene mutations. Exome sequencing results were further analysed by Sanger sequencing, computational studies, and in vitro functional studies such as immunofluorescence and enzyme assay. <b><i>Results:</i></b> We identified nine biallelic disease-causing variants in the <i>TPO</i> gene in 12 patients from nine unrelated Indian families. Eight of the nine variants were novel. No recurrent variants were identified. Computational analysis of six missense variants showed that these amino acid substitutions caused changes in non-covalent interactions with the adjacent residues that may affect the TPO protein structure and function. In vitro experimental data using immunofluorescence assay showed that these variants did not affect the plasma membrane localization of the TPO protein but caused a significant loss of TPO enzymatic activity compared to the wild type. <b><i>Conclusion:</i></b> Our study revealed multiple novel pathogenic variants in <i>TPO</i> gene in Indian patients, thereby expanding the genotype spectrum. Functional studies helped us to reveal the pathogenicity of the missense variants.