Department of Cell Biology, Howard Hughes Medical Institute, and Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
Department of Cell Biology, Howard Hughes Medical Institute, and Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
Curr Biol. 2017 Jan 23;27(2):291-297. doi: 10.1016/j.cub.2016.11.048. Epub 2017 Jan 5.
Germ cell death occurs in many species [1-3] and has been proposed as a mechanism by which the fittest, strongest, or least damaged germ cells are selected for transmission to the next generation. However, little is known about how the choice is made between germ cell survival and death. Here, we focus on the mechanisms that regulate germ cell survival during embryonic development in Drosophila. We find that the decision to die is a germ cell-intrinsic process linked to quantitative differences in germ plasm inheritance, such that higher germ plasm inheritance correlates with higher primordial germ cell (PGC) survival probability. We demonstrate that the maternal factor lipid phosphate phosphatase Wunen-2 (Wun2) regulates PGC survival in a dose-dependent manner. Since wun2 mRNA levels correlate with the levels of other maternal determinants at the single-cell level, we propose that Wun2 is used as a readout of the overall germ plasm quantity, such that only PGCs with the highest germ plasm quantity survive. Furthermore, we demonstrate that Wun2 and p53, another regulator of PGC survival, have opposite yet independent effects on PGC survival. Since p53 regulates cell death upon DNA damage and various cellular stresses, we hypothesize that together they ensure selection of the PGCs with highest germ plasm quantity and least cellular damage.
生殖细胞死亡发生在许多物种中[1-3],并被提出作为一种机制,通过该机制选择最适合、最强壮或受损伤最小的生殖细胞传递给下一代。然而,对于如何在生殖细胞存活和死亡之间做出选择,我们知之甚少。在这里,我们专注于调节果蝇胚胎发育过程中生殖细胞存活的机制。我们发现,死亡的决定是一个内在的生殖细胞过程,与生殖质遗传的定量差异有关,即更高的生殖质遗传与更高的原始生殖细胞(PGC)存活概率相关。我们证明了母体因子脂磷酸酶 Wunen-2(Wun2)以剂量依赖的方式调节 PGC 的存活。由于 wun2 mRNA 水平与单细胞水平上其他母体决定因素的水平相关,我们提出 Wun2 被用作整体生殖质数量的读出器,只有具有最高生殖质数量的 PGC 才能存活。此外,我们证明 Wun2 和另一种 PGC 存活调节剂 p53 对 PGC 存活具有相反但独立的影响。由于 p53 在 DNA 损伤和各种细胞应激下调节细胞死亡,我们假设它们共同确保选择具有最高生殖质数量和最小细胞损伤的 PGC。