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Retinoic acid regulates sex-specific timing of meiotic initiation in mice.

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TLDR
In this paper, the authors examined the mechanism underlying the sex-specific timing of Stra8 expression and meiotic initiation in mice and showed that signaling by retinoic acid (RA), an active derivative of vitamin A, is required for Stra8expression and thereby meiosis initiation in embryonic ovaries.
Abstract
In mammals, meiosis is initiated at different time points in males and females, but the mechanism underlying this difference is unknown. Female germ cells begin meiosis during embryogenesis. In males, embryonic germ cells undergo G0/G1 mitotic cell cycle arrest, and meiosis begins after birth. In mice, the Stimulated by Retinoic Acid Gene 8 (Stra8) has been found to be required for the transition into meiosis in both female and male germ cells. Stra8 is expressed in embryonic ovaries just before meiotic initiation, whereas its expression in testes is first detected after birth. Here we examine the mechanism underlying the sex-specific timing of Stra8 expression and meiotic initiation in mice. Our work shows that signaling by retinoic acid (RA), an active derivative of vitamin A, is required for Stra8 expression and thereby meiotic initiation in embryonic ovaries. We also discovered that RA is sufficient to induce Stra8 expression in embryonic testes and in vitamin A-deficient adult testes in vivo. Finally, our results show that cytochrome p450 (CYP)-mediated RA metabolism prevents premature Stra8 expression in embryonic testes. Treatment with an inhibitor specific to RA-metabolizing enzymes indicates that a cytochrome p450 from the 26 family (CYP26) is responsible for delaying Stra8 expression in embryonic testes. Sex-specific regulation of RA signaling thus plays an essential role in meiotic initiation in embryonic ovaries and precludes its occurrence in embryonic testes. Because RA signaling regulates Stra8 expression in both embryonic ovaries and adult testes, this portion of the meiotic initiation pathway may be identical in both sexes.

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Journal ArticleDOI

Retinoic Acid Synthesis and Signaling during Early Organogenesis

TL;DR: Recent studies suggest that retinoic acid may act primarily in a paracrine manner and provide insight into the cell-cell signaling networks that control differentiation of pluripotent cells.
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.
Journal ArticleDOI

Retinoic acid in development: towards an integrated view

TL;DR: Retinoic acid has complex and pleiotropic functions during vertebrate development and some of these functions could be maintained throughout the life of an organism to regulate cell-lineage decisions and/or the differentiation of stem cell populations, highlighting possibilities for regenerative medicine.
Journal ArticleDOI

Sex Determination and Gonadal Development in Mammals

TL;DR: The growing body of knowledge relating to testis development and the beginnings of a picture of ovary development together illustrate the complex mechanisms by which these organ systems develop, inform the etiology, diagnosis, and management of disorders of sexual development, and help define what it is to be male or female.
Journal ArticleDOI

Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice

TL;DR: It is concluded that, in mice, Stra8 regulates meiotic initiation in both spermatogenesis and oogenesis, and, in both the male and female germ lines, meiosis is initiated through retinoic acid induction of Stra8.
References
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Journal ArticleDOI

Retinoids in Embryonal Development

TL;DR: The key role of vitamin A in embryonal development is reviewed and special emphasis is given to the physiological action of retinoids, as evident from the retinoid ligand knockout models.
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Detection of messenger RNA by in situ hybridization to tissue sections and whole mounts.

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