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Building pathways for ovary organogenesis in the mouse embryo.

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TLDR
The history of studying ovary organogenesis in mammals is reviewed and the most recent discoveries using the mouse as the model organism are presented.
Abstract
Despite its significant role in oocyte generation and hormone production in adulthood, the ovary, with regard to its formation, has received little attention compared to its male counterpart, the testis. With the exception of germ cells, which undergo a female-specific pattern of meiosis, morphological changes in the fetal ovary are subtle. Over the past 40 years, a number of hypotheses have been proposed for the organogenesis of the mammalian ovary. It was not until the turn of the millennium, thanks to the advancement of genetic and genomic approaches, that pathways for ovary organogenesis that consist of positive and negative regulators have started to emerge. Through the action of secreted factors (R-spondin1, WNT4, and follistatin) and transcription regulators (β-catenin and FOXL2), the developmental fate of the somatic cells is directed toward ovarian, while testicular components are suppressed. In this chapter, we review the history of studying ovary organogenesis in mammals and present the most recent discoveries using the mouse as the model organism.

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Journal ArticleDOI

Temporal transcriptional profiling of somatic and germ cells reveals biased lineage priming of sexual fate in the fetal mouse gonad.

TL;DR: This study provides a molecular explanation reconciling the female default and balanced models of sex determination and represents a rich resource for the field, yielding new insights into the mechanisms by which different cell types in a single organ adopt their respective fates.
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Temporal Differences in Granulosa Cell Specification in the Ovary Reflect Distinct Follicle Fates in Mice

TL;DR: Findings from tamoxifen-induced lineage tracing of Foxl2-expressing cells show that descendants of the bipotential supporting cell precursors in the early gonad contribute granulosa cells to a specific population of follicles in the medulla of the ovary that begin to grow immediately after birth.
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EMT in developmental morphogenesis

Yukiko Nakaya, +1 more
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Lineage specification of ovarian theca cells requires multicellular interactions via oocyte and granulosa cells

TL;DR: These studies provide the first genetic evidence for the origins of theca cells and reveal a multicellular interaction critical for the formation of a functional theca.
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Mammalian foetal ovarian development: consequences for health and disease

TL;DR: A better understanding of these early cellular and morphological events will facilitate further study into the regulation of oocyte development, manifestation of ovarian disease and basis of female infertility.
References
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Journal ArticleDOI

Female development in mammals is regulated by Wnt-4 signalling

TL;DR: In the mammalian embryo, both sexes are initially morphologically indistinguishable: specific hormones are required for sex-specific development but the establishment of sexual dimorphism is under the control of both local and systemic signals.
Journal ArticleDOI

Germline stem cells and follicular renewal in the postnatal mammalian ovary

TL;DR: It is shown that juvenile and adult mouse ovaries possess mitotically active germ cells that, based on rates of oocyte degeneration (atresia) and clearance, are needed to continuously replenish the follicle pool.
Book

Principles of Development

Lewis Wolpert
TL;DR: In this paper, the Drosophila body plan was described and the Xenopus and zebrafish were shown to complete the body plan in the early stages of the development of the human embryo.
Journal ArticleDOI

Effect of single and compound knockouts of estrogen receptors alpha (ERalpha) and beta (ERbeta) on mouse reproductive phenotypes.

TL;DR: Results reveal a functional redundancy between ERalpha and ERbeta for ovarian folliculogenesis, and strongly suggest that ERbeta plays an important role in mediating the stimulatory effects of estrogens on granulosa cell proliferation.
Journal ArticleDOI

Retinoid Signaling Determines Germ Cell Fate in Mice

TL;DR: It is found that retinoic acid, produced by mesonephroi of both sexes, causes germ cells in the ovary to enter meiosis and inititate oogenesis, and precise regulation of retinoid levels during fetal gonad development provides the molecular control mechanism that specifies germ cell fate.
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