The Mitochondrial Genetics Group, Robinson Research Institute, School of Medicine, Adelaide Health and Medical Sciences Building, The University of Adelaide, Adelaide, SA 5005, Australia.
Cells. 2019 Aug 8;8(8):852. doi: 10.3390/cells8080852.
Mitochondria and mitochondrial DNA have important roles to play in development. In primordial germ cells, they progress from small numbers to populate the maturing oocyte with high numbers to support post-fertilization events. These processes take place under the control of significant changes in DNA methylation and other epigenetic modifiers, as well as changes to the DNA methylation status of the nuclear-encoded mitochondrial DNA replication factors. Consequently, the differentiating germ cell requires significant synchrony between the two genomes in order to ensure that they are fit for purpose. In this review, I examine these processes in the context of female germline stem cells that are isolated from the ovary and those derived from embryonic stem cells and reprogrammed somatic cells. Although our knowledge is limited in this respect, I provide predictions based on other cellular systems of what is expected and provide insight into how these cells could be used in clinical medicine.
线粒体和线粒体 DNA 在发育中起着重要的作用。在原始生殖细胞中,它们的数量从少到多,以充满成熟卵子,从而支持受精后的事件。这些过程发生在 DNA 甲基化和其他表观遗传修饰物的显著变化以及核编码线粒体 DNA 复制因子的 DNA 甲基化状态的变化的控制下。因此,分化的生殖细胞需要两个基因组之间的高度同步,以确保它们适合作特定用途。在这篇综述中,我在从卵巢中分离出来的雌性生殖干细胞和来自胚胎干细胞和重新编程体细胞的衍生生殖干细胞的背景下研究这些过程。尽管在这方面我们的知识有限,但我根据其他细胞系统提供了预期的预测,并深入了解这些细胞如何在临床医学中应用。