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Can Unlikely Neanderthal Chloride Channel CLC-2 Gene Variants Provide Insights in Modern Human Infertility?
Jeworutzki, Elena; Tüttelmann, Frank; Rothenberg, Ina; Pusch, Michael; Schreiber, Julian A; Kliesch, Sabine; Wünsch, Bernhard; Strutz-Seebohm, Nathalie; Seebohm, Guiscard.
Afiliação
  • Jeworutzki E; Cellular Electrophysiology and Molecular Biology, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.
  • Tüttelmann F; Institute of Reproductive Genetics, University of Münster, Münster, Germany.
  • Rothenberg I; Cellular Electrophysiology and Molecular Biology, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.
  • Pusch M; Istituto di Biofisica, Consiglio Nazionale delle Ricerche, Genova, Italy.
  • Schreiber JA; Cellular Electrophysiology and Molecular Biology, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.
  • Kliesch S; Institute of Pharmaceutical and Medicinal Chemistry, University of Münster, Münster, Germany.
  • Wünsch B; Centre of Reproductive Medicine and Andrology, Department of Clinical and Surgical Andrology, University Hospital Münster, Münster, Germany.
  • Strutz-Seebohm N; Institute of Pharmaceutical and Medicinal Chemistry, University of Münster, Münster, Germany.
  • Seebohm G; Cellular Electrophysiology and Molecular Biology, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.
Cell Physiol Biochem ; 55(3): 301-310, 2021 Jun 19.
Article em En | MEDLINE | ID: mdl-34148308
BACKGROUND/AIMS: Neanderthals, although well adapted to local environments, were rapidly replaced by anatomically modern humans (AMH) for unknown reasons. Genetic information on Neanderthals is limited restricting applicability of standard population genetics. METHODS: Here, we apply a novel combination of restricted genetic analyses on preselected physiological key players (ion channels), electrophysiological analyses of gene variants of unclear significance expressed in Xenopus laevis oocytes using two electrode voltage clamp and transfer of results to AMH genetics. Using genetic screening in infertile men identified a loss of CLC-2 associated with sperm deficiency. RESULTS: Increased genetic variation caused functionally impaired Neanderthals CLC-2 channels. CONCLUSION: Increased genetic variation could reflect an adaptation to different local salt supplies at the cost of reduced sperm density. Interestingly and consistent with this hypothesis, lack of CLC-2 protein in a patient associates with high blood K+ concentration and azoospermia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Canais de Cloreto / Homem de Neandertal / Infertilidade Masculina Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Canais de Cloreto / Homem de Neandertal / Infertilidade Masculina Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article