母体 vGluT2 和胚胎 mGluR3 信号中继系统控制豌豆蚜后代翅膀的二态性

Yiyang Yuan, Yanyan Wang, Wanwan Ye, Liqiang Xie, Erliang Yuan, Huijuan Guo, Shifan Wang, Fang Dong, Keyan Zhu-Salzman, Feng Ge, Yucheng Sun
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摘要

跨代表型可塑性(Transgenerational phenotypic plasticity,TPP)是指一代人所经历的环境条件可以影响后代人的表型,使其适应环境而不改变其 DNA 序列的现象。蚜虫翅膀的二态性是 TPP 的典型例子,母蚜通过感知环境线索来决定其后代的翅膀形态。然而,从母体到子代的信号传递机制仍不清楚。在这项研究中,我们发现种群密度和物理接触会导致豌豆蚜 Acyrthosiphon pisum 的后代中长翅的比例很高。通过组织特异性 RNA-seq 技术,我们发现独居蚜虫和密集饲养的母蚜头部和胚胎中的谷氨酸囊泡转运体 2(ApvGluT2)和代谢型谷氨酸受体 3(ApmGluR3)表达基因存在差异。大脑 ApvGluT2 和胚胎 ApmGluR3 表达的升高导致有翅比例的增加。敲除其中一种基因可抑制胚胎中 ApFoxO 的磷酸化。此外,EMSA显示,去磷酸化的ApFoxO直接与刺猬(ApHh)的启动子结合,抑制其在20期胚胎中的转录,导致长翅比例降低。我们的研究结果表明,脑vGluT2和胚胎mGluR3协调传递母体物理接触信号并控制子代的翅膀发育,展示了蚜虫依赖物理接触的跨代翅膀二态性的新型调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The maternal vGluT2 and embryonic mGluR3 signaling relay system controls offspring wing dimorphism in pea aphid
Transgenerational phenotypic plasticity (TPP) refers to the phenomenon that environmental conditions experienced by one generation can influence the phenotype of subsequent generations to adapt to the environment without modification of their DNA sequences. Aphid wing dimorphism is a textbook example of TPP by which a maternal aphid perceives the environmental cues to decide the wing morph of her offspring. However, the signaling mechanism from mother to daughter remains unclear. In this study, we showed that the population density and physical contact caused high proportion of winged offspring in the pea aphid Acyrthosiphon pisum. Its vesicular glutamate transporter 2 (ApvGluT2) and metabotropic glutamate receptor 3 (ApmGluR3) were identified by tissue-specific RNA-seq as differentially expressed genes in the head and embryo respectively between solitary and more densely housed maternal aphids. Elevated expression of brain ApvGluT2 and embryonic ApmGluR3 led to increases in the winged proportion. Knockdown of either gene inhibited phosphorylation of ApFoxO in embryos. Furthermore, EMSA showed that dephosphorylated ApFoxO directly bound to the promotor of hedgehog (ApHh), a morphogen gene for wing development, to repress its transcription in stage 20 embryos, causing a lower winged proportion. Our results demonstrated that brain vGluT2 and embryonic mGluR3 coordinately relayed the maternal physical contact signals and control wing development in offspring, showcasing a novel regulatory mechanism underlying physical contact-dependent, transgenerational wing dimorphism in aphids.
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