Mapping the anatomical and transcriptional landscape of early human fetal ovary development

The complex genetic mechanisms underlying human ovary development can give rise to clinical phenotypes if disrupted, such as Primary (or Premature) Ovarian Insufficiency and Differences of Sex Development. We combine single-nuclei RNA sequencing, bulk RNA sequencing, and micro-focus computed tomography to elucidate the anatomy and transcriptional landscape of the human fetal ovary across key developmental timepoints (Carnegie Stage 22 until 20 weeks post conception). We show the marked growth and distinct morphological changes within the fetal ovary at the critical timepoint of germ cell expansion and demonstrate that the fetal ovary becomes more transcriptomically distinct from the testis with age. We describe previously uncharacterised ovary developmental pathways, relating to neuroendocrine signalling, energy homeostasis, mitochondrial networks, and inflammasome regulation. We define transcriptional regulators and candidate genes for meiosis within the developing ovary. Together, this work advances our fundamental understanding of human ovary development and has relevance for human ovarian insufficiency phenotypes.

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Publication Details

Journal
Scientific Reports
Published
2025-05-06
DOI
https://doi.org/10.1038/s41598-025-96135-y
Citations
3
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
5.64

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article

Mapping the anatomical and transcriptional landscape of early human fetal ovary development

Ian C. Simcock, John C. Achermann, Theodoros Xenakis, Federica Buonocore et al.
3 citations
Scientific Reports
Reproductive Biology and Fertility
5.64
article

Mapping the anatomical and transcriptional landscape of early human fetal ovary development

Ian C. Simcock, John C. Achermann, Theodoros Xenakis, Federica Buonocore, Ignacio del Valle, Owen J. Arthurs, Jenifer P. Suntharalingham, Nadjeda Moreno, Sinead McGlacken‐Byrne, Paola Niola, Gerard Conway, Mehul Dattani, Berta Crespo, Nita Solanky, Danielle Liptrot, Tony Brooks
article en
3 citations

Abstract

The complex genetic mechanisms underlying human ovary development can give rise to clinical phenotypes if disrupted, such as Primary (or Premature) Ovarian Insufficiency and Differences of Sex Development. We combine single-nuclei RNA sequencing, bulk RNA sequencing, and micro-focus computed tomography to elucidate the anatomy and transcriptional landscape of the human fetal ovary across key developmental timepoints (Carnegie Stage 22 until 20 weeks post conception). We show the marked growth and distinct morphological changes within the fetal ovary at the critical timepoint of germ cell expansion and demonstrate that the fetal ovary becomes more transcriptomically distinct from the testis with age. We describe previously uncharacterised ovary developmental pathways, relating to neuroendocrine signalling, energy homeostasis, mitochondrial networks, and inflammasome regulation. We define transcriptional regulators and candidate genes for meiosis within the developing ovary. Together, this work advances our fundamental understanding of human ovary development and has relevance for human ovarian insufficiency phenotypes.

Scientific ReportsVol. 15(1)
Great Ormond Street Hospital for Children NHS Foundation Trust (GB), Institute of Child Health (IN), University College London (GB)
Wellcome Trust, National Institute for Health and Care Research, Medical Research Council, NIHR Great Ormond Street Hospital Biomedical Research Centre
Openalex Percentile: Top 5%
Reproductive Biology and Fertility
5.64
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