Swartz S Zachary, Wessel Gary M
Department of Molecular and Cellular Biology, Brown University, Providence, Rhode Island, USA.
Department of Molecular and Cellular Biology, Brown University, Providence, Rhode Island, USA.
Curr Top Dev Biol. 2015;113:149-90. doi: 10.1016/bs.ctdb.2015.06.003. Epub 2015 Aug 19.
With few exceptions, all animals acquire the ability to produce eggs or sperm at some point in their life cycle. Despite this near-universal requirement for sexual reproduction, there exists an incredible diversity in germ line development. For example, animals exhibit a vast range of differences in the timing at which the germ line, which retains reproductive potential, separates from the soma, or terminally differentiated, nonreproductive cells. This separation may occur during embryonic development, after gastrulation, or even in adults, depending on the organism. The molecular mechanisms of germ line segregation are also highly diverse, and intimately intertwined with the overall transition from a fertilized egg to an embryo. The earliest embryonic stages of many species are largely controlled by maternally supplied factors. Later in development, patterning control shifts to the embryonic genome and, concomitantly with this transition, the maternally supplied factors are broadly degraded. This chapter attempts to integrate these processes--germ line segregation, and how the divergence of germ line and soma may utilize the egg to embryo transitions differently. In some embryos, this difference is subtle or maybe lacking altogether, whereas in other embryos, this difference in utilization may be a key step in the divergence of the two lineages. Here, we will focus our discussion on the echinoderms, and in particular the sea urchins, in which recent studies have provided mechanistic understanding in germ line determination. We propose that the germ line in sea urchins requires an acquisition of maternal factors from the egg and, when compared to other members of the taxon, this appears to be a derived mechanism. The acquisition is early--at the 32-cell stage--and involves active protection of maternal mRNAs, which are instead degraded in somatic cells with the maternal-to-embryonic transition. We collectively refer to this model as the Time Capsule method for germ line determination.
除少数例外情况外,所有动物在其生命周期的某个阶段都具备产生卵子或精子的能力。尽管有性生殖几乎是普遍需求,但生殖细胞系的发育却存在令人难以置信的多样性。例如,动物在具有生殖潜力的生殖细胞系与体细胞(即终末分化的非生殖细胞)分离的时间上表现出巨大差异。这种分离可能发生在胚胎发育期间、原肠胚形成之后,甚至在成体阶段,具体取决于生物体。生殖细胞系分离的分子机制也高度多样,并且与从受精卵到胚胎的整体转变密切相关。许多物种的早期胚胎阶段在很大程度上受母体提供的因素控制。在发育后期,模式控制转移到胚胎基因组,与此同时,母体提供的因素会广泛降解。本章试图整合这些过程——生殖细胞系的分离,以及生殖细胞系和体细胞的分化如何以不同方式利用从卵子到胚胎的转变。在一些胚胎中,这种差异很细微或可能完全不存在,而在其他胚胎中,这种利用上的差异可能是两个谱系分化的关键步骤。在这里,我们将把讨论重点放在棘皮动物,特别是海胆上,最近的研究为海胆生殖细胞系的确定提供了机制上的理解。我们提出,海胆的生殖细胞系需要从卵子中获取母体因素,与该分类群的其他成员相比,这似乎是一种衍生机制。这种获取发生得很早——在32细胞阶段——并且涉及对母体mRNA的主动保护,而这些mRNA在从母体到胚胎的转变过程中在体细胞中会被降解。我们将这个模型统称为生殖细胞系确定的时间胶囊方法。