Division of Molecular Genetics and Development, and ARC Centre of Excellence in Biotechnology and Development, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland 4072, Australia.
Reproduction. 2010 Jun;139(6):943-58. doi: 10.1530/REP-10-0075. Epub 2010 Apr 15.
Mammalian germ cells do not determine their sexual fate based on their XX or XY chromosomal constitution. Instead, sexual fate is dependent on the gonadal environment in which they develop. In a fetal testis, germ cells commit to the spermatogenic programme of development during fetal life, although they do not enter meiosis until puberty. In a fetal ovary, germ cells commit to oogenesis by entering prophase of meiosis I. Although it was believed previously that germ cells are pre-programmed to enter meiosis unless they are actively prevented from doing so, recent results indicate that meiosis is triggered by a signaling molecule, retinoic acid (RA). Meiosis is avoided in the fetal testis because a male-specifically expressed enzyme actively degrades RA during the critical time period. Additional extrinsic factors are likely to influence sexual fate of the germ cells, and in particular, we postulate that an additional male-specific fate-determining factor or factors is involved. The full complement of intrinsic factors that underlie the competence of gonadal germ cells to respond to RA and other extrinsic factors is yet to be defined.
哺乳动物生殖细胞的性别命运并非由其 XX 或 XY 染色体组成决定,而是取决于其发育所处的性腺环境。在胎儿睾丸中,生殖细胞在胎儿期就开始向精子发生的发育程序定向,但直到青春期才进入减数分裂。在胎儿卵巢中,生殖细胞通过进入减数分裂 I 的前期而向卵子发生定向。尽管以前认为生殖细胞如果没有被主动阻止,就会预先编程进入减数分裂,但最近的结果表明,减数分裂是由一种信号分子——视黄酸(RA)触发的。在胎儿睾丸中,减数分裂被避免,因为一种雄性特异性表达的酶在关键时期积极降解 RA。其他外在因素可能会影响生殖细胞的性别命运,特别是我们假设存在额外的雄性特异性命运决定因子或因子参与其中。决定性腺生殖细胞对 RA 和其他外在因素作出反应能力的内在因子的完整组成仍有待确定。