Department of Biology and W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina, United States of America.
PLoS One. 2010 May 17;5(5):e10674. doi: 10.1371/journal.pone.0010674.
Polistes paper wasps are models for understanding conditions that may have characterized the origin of worker and queen castes and, therefore, the origin of paper wasp sociality. Polistes is "primitively eusocial" by virtue of having context-dependent caste determination and no morphological differences between castes. Even so, Polistes colonies have a temporal pattern in which most female larvae reared by the foundress become workers, and most reared by workers become future-reproductive gynes. This pattern is hypothesized to reflect development onto two pathways, which may utilize mechanisms that regulate diapause in other insects. Using expressed sequence tags (ESTs) for Polistes metricus we selected candidate genes differentially expressed in other insects in three categories: 1) diapause vs. non-diapause phenotypes and/or worker vs. queen differentiation, 2) behavioral subcastes of worker honey bees, and 3) no a priori expectation of a role in worker/gyne development. We also used a non-targeted proteomics screen to test for peptide/protein abundance differences that could reflect larval developmental divergence. We found that foundress-reared larvae (putative worker-destined) and worker-reared larvae (putative gyne-destined) differed in quantitative expression of sixteen genes, twelve of which were associated with caste and/or diapause in other insects, and they also differed in abundance of nine peptides/proteins. Some differentially-expressed genes are involved in diapause regulation in other insects, and other differentially-expressed genes and proteins are involved in the insulin signaling pathway, nutrient metabolism, and caste determination in highly social bees. Differential expression of a gene and a peptide encoding hexameric storage proteins is especially noteworthy. Although not conclusive, our results support hypotheses of 1) larval developmental pathway divergence that can lead to caste bias in adults and 2) nutritional differences as the foundation of the pathway divergence. Finally, the differential expression in Polistes larvae of genes and proteins also differentially expressed during queen vs. worker caste development in honey bees may indicate that regulatory mechanisms of caste outcomes share similarities between primitively eusocial and advanced eusocial Hymenoptera.
Polistes 纸蜂是理解可能具有特征的条件的模型,这些条件决定了工蜂和蜂王的起源,因此也决定了纸蜂社会性的起源。Polistes 由于具有依赖环境的等级决定和等级之间没有形态差异,因此是“原始真社会性”的。即便如此,Polistes 群体仍存在时间模式,其中大多数由创始人饲养的雌性幼虫成为工蜂,而大多数由工蜂饲养的幼虫成为未来有生殖能力的雌蜂。这种模式被假设反映了两条途径的发育,这两条途径可能利用了在其他昆虫中调节休眠的机制。使用 Polistes metricus 的表达序列标签(EST),我们选择了在三个类别中在其他昆虫中差异表达的候选基因:1)休眠与非休眠表型和/或工蜂与蜂王分化,2)工蜂的行为亚等级,3)没有事先预期在工蜂/雌蜂发育中起作用。我们还使用非靶向蛋白质组学筛选来测试肽/蛋白质丰度差异,这些差异可能反映幼虫发育的差异。我们发现,创始人饲养的幼虫(推测为工蜂定向)和工蜂饲养的幼虫(推测为雌蜂定向)在十六个基因的定量表达上存在差异,其中十二个基因与其他昆虫中的等级和/或休眠有关,它们在九个肽/蛋白质的丰度上也存在差异。一些差异表达的基因参与其他昆虫的休眠调节,而其他差异表达的基因和蛋白质参与胰岛素信号通路、营养代谢和高度社会性蜜蜂的等级决定。差异表达的基因和编码六聚体储存蛋白的肽尤其值得注意。尽管没有结论性,但我们的结果支持以下假设:1)幼虫发育途径的差异,可导致成虫的等级偏见,2)营养差异是途径差异的基础。最后,Polistes 幼虫中差异表达的基因和蛋白质也在蜜蜂中蜂王与工蜂等级发育过程中差异表达,这可能表明等级结果的调控机制在原始真社会性和高级真社会性膜翅目昆虫之间具有相似性。