iScience (Jul 2023)

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

  • Junyan Liu,
  • Fazal Rahim,
  • Jianteng Zhou,
  • Suixing Fan,
  • Hanwei Jiang,
  • Changping Yu,
  • Jing Chen,
  • Jianze Xu,
  • Gang Yang,
  • Wasim Shah,
  • Muhammad Zubair,
  • Asad Khan,
  • Yang Li,
  • Basit Shah,
  • Daren Zhao,
  • Furhan Iqbal,
  • Xiaohua Jiang,
  • Tonghang Guo,
  • Peng Xu,
  • Bo Xu,
  • Limin Wu,
  • Hui Ma,
  • Yuanwei Zhang,
  • Huan Zhang,
  • Qinghua Shi

Journal volume & issue
Vol. 26, no. 7
p. 107193

Abstract

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Summary: 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 KCTD19 (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 KCTD19 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 Kctd19 mutant mouse testes and affected individual testes. Collectively, our findings demonstrate the pathogenicity of the identified KCTD19 variants and highlight an essential role of KCTD19 in MMI chromosome individualization.

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