
In the developing mammalian testis, only a tiny proportion of fetal and neonatal prospermatogonia give rise to the foundational pool of spermatogonial stem cells (SSCs). Multiple lines of evidence have suggested that determining which prospermatogonia give rise to foundational SSCs is not random but somewhat predetermined, such that foundational SSCs are ensured to develop advantageous characteristics such as enhanced genetic integrity. This study suggests that differential epigenetic programming and epigenetic priming contribute to the molecular mechanisms by which an early subset of developing prospermatogonia becomes predetermined to form the foundational pool of SSCs.
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