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Germ Cell Commitment to Oogenic Versus Spermatogenic Pathway: The Role of Retinoic Acid

机译:生殖细胞对ofogenic的致力于of pepermatic途径:视黄酸的作用

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摘要

The core of the decision to commit to either oogenesis or spermatogen-esis lies in the timing of meiotic entry. Primordial germ cells within the fetal ovary become committed to the female pathway prior to birth and enter meiosis during embryonic development. In the fetal testis, however, the germ cells are protected from this signal before birth and instead receive this trigger postnatally. There is a growing body of evidence to indicate that RA is the meiosis-inducing factor in both sexes, with the gender-specific timing of meiotic entry controlled via degradation of this molecule only within the fetal testis. This chapter will review our current understanding of how RA controls germ cell fate in both the embryonic ovary and postnatal testis, highlighting the key studies that have led to the hypothesis that RA can drive the commitment to meiosis in both sexes and discussing the current debate over whether RA truly is the meiosis-inducing factor in the fetal ovary.
机译:决定犯罪的核心是对ofercesis或精子素-sers的核心位于减数分裂的时序。 胎儿卵巢内的原始生殖细胞变为在出生前的雌性途径,进入胚胎发育期间的减数分裂。 然而,在胎儿睾丸中,胚芽细胞在出生前免受该信号的保护,而是在出生之前从该信号中保护。 有一种不断增长的证据表明RA是两性的诱导因子,具有通过仅在胎儿睾丸内降解该分子的减数分裂进入的性别特异性时序。 本章将审查我们目前对RA对胚胎卵巢和产后睾丸进行胚芽细胞命运的了解,突出了导致RA能够在两性中致力于减数分裂的假设并讨论目前的辩论的关键研究 Ra真正是胎儿卵巢中的诱导因子。

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