Cooke Paul S, Nanjappa Manjunatha K
Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32608, USA.
Asian J Androl. 2015 May-Jun;17(3):441-2. doi: 10.4103/1008-682X.151401.
How the primordial germ cell (PGC) lineage, which eventually gives rise to spermatozoa in males and oocytes in females, is established in the developing mammalian embryo has been a critical topic in both developmental and reproductive biology for many years. There have been significant breakthroughs over the past two decades in establishing both the source of PGCs and the factors that regulate the specification of this lineage in mice, [1] but our understanding of the factors that control PGC development in the human is rudimentary. The SRY-related HMG-box (SOX) family of transcription factors consists of 20 genes in humans and mice that are involved in the maintenance of pluripotency, male sexual development, and other processes. A recent paper in Cell has identified one member of this family, SOX17, as an essential factor for inducing the PGC lineage in humans. [2] Surprisingly, this protein does not appear to have a role in PGC specification in mice. This work not only introduces a new and important player to the field of germ cell specification, but also emphasizes the uniqueness of human PGC development compared to more extensively studied mouse models.
原始生殖细胞(PGC)谱系最终在雄性中产生精子,在雌性中产生卵母细胞,它如何在发育中的哺乳动物胚胎中建立,多年来一直是发育生物学和生殖生物学中的关键课题。在过去二十年里,在确定小鼠中PGC的来源以及调节该谱系特化的因素方面取得了重大突破,[1]但我们对控制人类PGC发育的因素的了解还很初步。转录因子的SRY相关HMG盒(SOX)家族在人类和小鼠中由20个基因组成,这些基因参与多能性的维持、雄性性发育和其他过程。《细胞》杂志最近发表的一篇论文确定该家族的一个成员SOX17是诱导人类PGC谱系的关键因素。[2]令人惊讶的是,这种蛋白质在小鼠的PGC特化过程中似乎没有作用。这项工作不仅为生殖细胞特化领域引入了一个新的重要因素,还强调了与研究更广泛的小鼠模型相比,人类PGC发育的独特性。