{"id":26578,"date":"2025-06-15T12:35:45","date_gmt":"2025-06-15T06:50:45","guid":{"rendered":"https:\/\/www.revoscience.com\/en\/?p=26578"},"modified":"2025-06-15T12:35:50","modified_gmt":"2025-06-15T06:50:50","slug":"maternal-iron-levels-an-immense-influence-on-sex-determination-in-embryos","status":"publish","type":"post","link":"https:\/\/www.revoscience.com\/en\/maternal-iron-levels-an-immense-influence-on-sex-determination-in-embryos\/","title":{"rendered":"Maternal iron levels: an immense influence on sex determination in embryos"},"content":{"rendered":"\n
\"\"
Photograph of offspring born to iron chelator-treated mothers during pregnancy. Left, normally developed XY male animal; middle, intersex-phenotype XY animal; right, completely feminized XY animal. \u00a0IMAGE: Makoto Tachibana<\/sup><\/em><\/figcaption><\/figure>\n\n\n\n

Osaka, Japan\u2014 <\/strong>Developmentally expressed genes play a fundamental role in the formation of a wide range of organs. The Y chromosome-located mammalian sex-determining gene Sry, required for the formation of testes, is activated only within a narrow time window during embryogenesis. However, the processes behind the activation of Sry remain uncertain.<\/p>\n\n\n\n

Now, in a recent publication from\u00a0Nature<\/em>, a team from the University of Osaka has discovered that iron plays a crucial role in male mammalian sex development.<\/p>\n\n\n\n

The Sry gene directs sexually undifferentiated gonads to differentiate into testes rather than ovaries. The Sry gene is initially inactive because of a modification added to DNA-wrapping proteins called histone methylation. In males, a protein called KDM3A is responsible for removing this histone methylation, allowing the Sry gene to become active.<\/p>\n\n\n\n

\u201cWe already knew that KDM3A requires iron for its enzymatic activity,\u201d says lead author Naoki Okashita. \u201cTherefore, we wanted to investigate the extent and nature of iron metabolism and histone demethylation in sex determination.\u201d<\/p>\n\n\n\n

The researchers established mice lacking Tfrc, a gene crucial for cellular iron incorporation. Loss of Tfrc prevented the removal of the histone methylation, leading to reduced Sry expression. When inspecting the genitals of these mice, it was found that some XY mice developed as females, despite being genetically male.<\/p>\n\n\n\n

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The role of iron metabolism in mouse male sex determination: intracellular iron elevation drives H3K9 demethylation required for Sry activation.<\/sup><\/em> IMAGE: Makoto Tachibana<\/sup><\/em><\/figcaption><\/figure>\n\n\n\n

The team also established an organ culture system for gonadal cells in which they could manipulate the levels of available iron. This confirmed that iron deficiency reduces the activity of KDM3A and activation of Sry. Therefore, the reduced Sry suppression under iron-deficient conditions was caused by the failure of KDM3A to remove histone methylation.<\/p>\n\n\n\n

Perhaps most significantly, they then showed that maternal iron deficiency\u2014whether induced by diet or by pharmacological intervention\u2014could lead to altered histone methylation of the Sry gene because of reduced KDM3A activity. Some populations of XY offspring derived from iron-deficient pregnant females were shown to undergo male-to-female sex reversal, potentially due to the impaired Sry activation.<\/p>\n\n\n\n

\u201cOur findings indicate that iron deficiency leads to disorders of male development, at least in mice. Our study emphasizes the importance of maintaining maternal iron levels,\u201d explains senior author Makoto Tachibana.<\/p>\n\n\n\n

It is known that in humans, Fanconi anemia and Diamond\u2013Blackfan anemia are risk factors for disorders of development. Understanding how iron supports embryonic development underscores the importance of maternal iron intake for the healthy development of human embryos.<\/p>\n\n\n\n

Reference:<\/strong><\/p>\n\n\n\n

The article, \u201cMaternal iron deficiency causes male-to-female sex reversal in mouse embryos\u201d, was published in\u00a0Nature\u00a0at DOI:\u00a0https:\/\/doi.org\/10.1038\/s41586-025-09063-2<\/a>.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

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