Active Pregnancy, Children & Inherited Conditions Genetics & Molecular Biology

The molecular anatomy of human genital development

In plain English

AI plain-English summary

Between the 8th and 16th week of pregnancy, the human genitals develop through a series of poorly understood steps that often go wrong, causing common birth variations like hypospadias. This project will map the molecular instructions that guide penis and clitoris formation, using a combination of gene activity analysis, high-resolution imaging, and lab models. The problem is that most genital variations have no known genetic cause, and current surgical options are difficult, with lasting psychological effects on body image and sexual function. Without a clear picture of how these tissues normally form, doctors lack the biological knowledge to offer better support or alternatives. If this work succeeds, it could reveal new causes of genital variations and lead to more nuanced clinical management—potentially reducing the need for invasive surgery and improving counselling for patients and families. The research is fundamentally curiosity-driven, exploring basic developmental biology. However, similar fundamental studies of embryonic development have previously uncovered unexpected links to adult health, and here the team will also investigate how genital development connects to sex differences in fat tissue and to complex urological conditions in women.

View original technical description
Human genital development shows marked differences compared to other species, but remains one of the least researched developmental processes. Variations in genital development, such as hypospadias are remarkably common. A clear genetic condition is sometimes responsible, but often the underlying cause is unknown. Most variations in genital development result from altered developmental processes between 8-16 weeks post conception. These are anatomically complex and poorly understood. Current surgical interventions, if undertaken, are challenging. Psychological consequences need to be considered (e.g. body-image, urological and sexual function), but greater nuanced support is needed. To address these challenges we propose a multimodal, integrated approach using transcriptomics, bio-imaging, model systems and clinical insight to: 1) define molecular mechanisms of penile urethral closure, penis growth and novel causes of hypospadias; 2) define the molecular basis of clitoral and urogenital sinus remodelling, clitoral/vaginal innervation, and consequences for complex uro-gynaecological conditions; 3) investigate sex differences in fetal adipose tissue development, which we feel are inherently linked to genital development; 4) develop our work on lived experiences, support and positive educational impact of our findings. We anticipate this project will lead to novel management options, and will have wider implications for understanding sex development/function.

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Researchers

John Achermann (EPMC Awardee)

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Original classification

Discovery Award

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