The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Division of Research, Economic Development, and Graduate Education, California Polytechnic State University, San Luis Obispo, CA, USA.
Hum Reprod Update. 2022 May 2;28(3):313-345. doi: 10.1093/humupd/dmac002.
The pathways of gametogenesis encompass elaborate cellular specialization accompanied by precise partitioning of the genome content in order to produce fully matured spermatozoa and oocytes. Transcription factors are an important class of molecules that function in gametogenesis to regulate intrinsic gene expression programs, play essential roles in specifying (or determining) germ cell fate and assist in guiding full maturation of germ cells and maintenance of their populations. Moreover, in order to reinforce or redirect cell fate in vitro, it is transcription factors that are most frequently induced, over-expressed or activated. Many reviews have focused on the molecular development and genetics of gametogenesis, in vivo and in vitro, in model organisms and in humans, including several recent comprehensive reviews: here, we focus specifically on the role of transcription factors. Recent advances in stem cell biology and multi-omic studies have enabled deeper investigation into the unique transcriptional mechanisms of human reproductive development. Moreover, as methods continually improve, in vitro differentiation of germ cells can provide the platform for robust gain- and loss-of-function genetic analyses. These analyses are delineating unique and shared human germ cell transcriptional network components that, together with somatic lineage specifiers and pluripotency transcription factors, function in transitions from pluripotent stem cells to gametes. This grand theme review offers additional insight into human infertility and reproductive disorders that are linked predominantly to defects in the transcription factor networks and thus may potentially contribute to the development of novel treatments for infertility.
配子发生途径包括精细的细胞特化,伴随着基因组内容的精确分配,以产生完全成熟的精子和卵子。转录因子是一类重要的分子,它们在配子发生中发挥作用,调节内在的基因表达程序,在决定生殖细胞命运方面发挥着重要作用,并有助于指导生殖细胞的完全成熟和维持其种群。此外,为了在体外加强或改变细胞命运,最常诱导、过表达或激活的是转录因子。许多评论都集中在模型生物和人类的体内和体外配子发生的分子发育和遗传学上,包括最近的一些综述:在这里,我们特别关注转录因子的作用。干细胞生物学和多组学研究的最新进展使我们能够更深入地研究人类生殖发育的独特转录机制。此外,随着方法的不断改进,生殖细胞的体外分化为强有力的基因功能获得和缺失分析提供了平台。这些分析描绘了独特和共享的人类生殖细胞转录网络组件,这些组件与体细胞谱系决定因子和多能性转录因子一起,在从多能干细胞到配子的转变中发挥作用。本综述进一步深入探讨了与转录因子网络缺陷主要相关的人类不育和生殖障碍,这可能有助于开发新的不育症治疗方法。