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Maternal Iron Deficiency Drives Male Mouse Embryos to Develop Ovaries

Low maternal iron in mice inactivated the SRY gene via the KDM3A enzyme, raising questions about similar effects in human pregnancies.

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An illustrative image of a laboratory mouse.
Baby mice born to iron-deficient moms didn't always have the sex organs that match their chromosomes in an new study led by researchers at Osaka University

Overview

  • Four out of 72 XY embryos in iron-deficient dams and six out of 39 embryos in low-iron gonad cultures developed ovaries instead of testes.
  • Iron depletion disrupted the iron-dependent KDM3A enzyme that activates the SRY gene, leading to its inactivation in some male embryos.
  • Published in Nature, the study offers the first mammalian evidence that environmental factors can override genetic sex determination.
  • Researchers caution that the small number of affected mice limits definitive conclusions and are planning further studies to explore human relevance.
  • Iron deficiency affects roughly 40% of human pregnancies worldwide, highlighting potential implications for fetal development and prenatal nutrition guidelines.