Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans

Abstract

Azoospermia is a significant cause of male infertility, with non-obstructive azoospermia (NOA) being the most severe type of spermatogenic failure. NOA is mostly caused by congenital factors, but our understanding of its genetic causes is very limited. Here, we identified a frameshift variant (c.201_202insAC, p.Tyr68Thrfs∗17) and two nonsense variants (c.1897C>T, p.Gln633∗; c.2005C>T, p.Gln669∗) in <i>KCTD19</i> (potassium channel tetramerization domain containing 19) from two unrelated infertile Chinese men and a consanguineous Pakistani family with three infertile brothers. Testicular histological analyses revealed meiotic metaphase I (MMI) arrest in the affected individuals. Mice modeling <i>KCTD19</i> variants recapitulated the same MMI arrest phenotype due to severe disrupted individualization of MMI chromosomes. Further analysis showed a complete loss of KCTD19 protein in both <i>Kctd19</i> mutant mouse testes and affected individual testes. Collectively, our findings demonstrate the pathogenicity of the identified <i>KCTD19</i> variants and highlight an essential role of <i>KCTD19</i> in MMI chromosome individualization.