Embryogenesis in Myrmicine Ants Combines Features of Short Germ-Band Development With a Progressive Mode of Segmentation.

IF 1.8 3区 生物学 Q3 DEVELOPMENTAL BIOLOGY
Chi-Chun Fang, Arjuna Rajakumar, Andrew Kenny, Ulrich G Mueller, Ehab Abouheif, David Stein
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引用次数: 0

Abstract

Ants exhibit complex social organization, morphologically and functionally distinct castes, and the exploitation of diverse ecological niches. How these features have influenced embryonic development relative to other insects remains unclear. Insect embryogenesis has been classified into three modes: In long germ-band development, exemplified by the fruit fly Drosophila melanogaster, segments along the entire anterior-posterior axis of the embryonic primordium are established almost simultaneously, before gastrulation, with the initial embryonic primordium surrounding almost the entire volume of the egg. In short and intermediate germ-band modes, the embryonic primordium occupies a smaller proportion of the egg surface, with anterior segments initially specified, and remaining segments being added sequentially from a posterior growth zone. Here, we examine embryogenesis in three myrmicine ants, the fungus-gardening ants Atta texana and Mycocepurus smithii, and the red imported fire ant Solenopsis invicta. We find that these ant embryos combine features of short germ-band development with a newly characterized progressive pattern of segmentation that has been associated with some long germ-band-developing insects. Despite similarities in the size of ant and Drosophila eggs, embryogenesis in the three ant species is 10- to 20-fold longer than in Drosophila and is also significantly longer than in two other hymenopteran species that have been studied, the honeybee Apis mellifera and the jewel wasp Nasonia vitripennis. Moreover, the embryos produced by A. texana foundress queens develop to first instar larvae 25% faster than embryos produced by mature queens. We discuss these results in the context of the eusocial lifestyle of ants.

金蚁的胚胎发育具有短胚带发育特征和渐进式分裂模式。
蚂蚁表现出复杂的社会组织,形态和功能上的等级差异,以及对生态位的利用。相对于其他昆虫,这些特征是如何影响胚胎发育的尚不清楚。昆虫的胚胎发生被分为三种模式:在长胚带发育中,以果蝇为例,在原肠胚形成之前,沿着整个胚胎原基的前后轴几乎同时建立,最初的胚胎原基几乎包围了卵的整个体积。在短种带和中间种带模式中,胚胎原基在卵子表面所占的比例较小,最初指定前段,其余部分从后生长区依次添加。在这里,我们研究了三种金蚁的胚胎发生,真菌园艺蚂蚁Atta texana和Mycocepurus smithii,以及红色进口火蚁Solenopsis invicta。我们发现这些蚂蚁胚胎结合了短胚芽带发育的特征和一种与一些长胚芽带发育的昆虫有关的新特征的渐进分割模式。尽管蚂蚁和果蝇卵的大小相似,但这三种蚂蚁的胚胎发育时间比果蝇长10到20倍,也比其他两种已被研究过的膜翅目物种——蜜蜂Apis mellifera和珠宝黄蜂Nasonia vitripennis——长得多。此外,德克萨斯褐家鼠创始蜂后产生的胚胎比成熟蜂后产生的胚胎发育到一龄幼虫的速度快25%。我们在蚂蚁的群居生活方式的背景下讨论这些结果。
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来源期刊
CiteScore
4.80
自引率
9.10%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Developmental Evolution is a branch of evolutionary biology that integrates evidence and concepts from developmental biology, phylogenetics, comparative morphology, evolutionary genetics and increasingly also genomics, systems biology as well as synthetic biology to gain an understanding of the structure and evolution of organisms. The Journal of Experimental Zoology -B: Molecular and Developmental Evolution provides a forum where these fields are invited to bring together their insights to further a synthetic understanding of evolution from the molecular through the organismic level. Contributions from all these branches of science are welcome to JEZB. We particularly encourage submissions that apply the tools of genomics, as well as systems and synthetic biology to developmental evolution. At this time the impact of these emerging fields on developmental evolution has not been explored to its fullest extent and for this reason we are eager to foster the relationship of systems and synthetic biology with devo evo.
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