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

机译:生殖细胞对生源和生精途径的承诺:维甲酸的作用

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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:致力于卵子发生或生精的决定的核心在于减数分裂进入的时间。胎儿卵巢内的原始生殖细胞在出生前就进入雌性途径,并在胚胎发育过程中进入减数分裂。但是,在胎儿的睾丸中,生殖细胞在出生前就受到保护而不受该信号的影响,而是在出生后接受这种触发。越来越多的证据表明,RA是男女两性的减数分裂诱导因子,减数分裂进入的性别特定时机仅通过该分子在胎儿睾丸内的降解来控制。本章将回顾我们目前对RA如何控制胚胎卵巢和产后睾丸中生殖细胞命运的理解,重点介绍导致RA可以推动性别减数分裂的假设的关键研究,并讨论当前关于RA的争论。 RA是否确实是胎儿卵巢中的减数分裂诱导因子。

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