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Drosophila Netrin-B controls mushroom body axon extension and regulates courtship-associated learning and memory of a Drosophila fragile X syndrome model

机译:果蝇Netrin-B控制蘑菇体轴突延伸并调节果蝇脆弱X综合征模型的求爱相关学习和记忆。

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摘要

Mushroom body (MB) is a prominent structure essential for olfactory learning and memory in the Drosophila brain. The development of the MB involves the appropriate guidance of axon lobes and sister axon branches. Appropriate guidance that accurately shapes MB development requires the integration of various guidance cues provided by a series of cell types, which guide axons to reach their final positions within the MB neuropils. Netrins are axonal guidance molecules that are conserved regulators of embryonic nerve cord patterning. However, whether they contribute to MB morphogenesis has not yet been evaluated. Here, we find that Netrin-B (NetB) is highly expressed in the MB lobes, regulating lobe length through genetic interactions with the receptors Frazzled and Uncoordinated-5 from 24 h after pupal formation onwards. We observe that overexpression of NetB causes severe β lobe fusion in the MB, which is similar to the MB defects seen in the Drosophila model of fragile X syndrome (FXS). Our results further show that fragile-X mental retardation protein FMRP inhibits the translational activity of human ortholog Netrin-1 (NTN1). Knock-down of NetB significantly rescues the MB defects and ameliorates deficits in the learning and memory in FXS model Drosophila. These results indicate a critical role for NetB in MB lobe extension and identify NetB as a novel target of FMRP which contributes to learning and memory.Electronic supplementary materialThe online version of this article (10.1186/s13041-019-0472-1) contains supplementary material, which is available to authorized users.
机译:蘑菇体(MB)是果蝇大脑嗅觉学习和记忆必不可少的重要结构。 MB的发展涉及轴突叶和姊妹轴突分支的适当指导。正确地指导MB发育的适当指导需要整合由一系列细胞类型提供的各种指导线索,这些指导线索将指导轴突到达MB神经桩内的最终位置。 Netrins是轴突引导分子,是胚胎神经线形成的保守调节因子。但是,尚未评估它们是否有助于MB形态发生。在这里,我们发现Netrin-B(NetB)在MB肺叶中高表达,通过p形成后24h内与受体Frazzled和Uncoordinated-5的遗传相互作用调节肺叶长度。我们观察到NetB的过表达会导致MB中严重的β叶片融合,这与在易碎X综合征(FXS)的果蝇模型中看到的MB缺陷相似。我们的结果进一步表明,脆性X智力低下蛋白FMRP抑制人类直系同源蛋白Netrin-1(NTN1)的翻译活性。击倒NetB可以大大挽救MB缺陷,并改善FXS模型果蝇的学习和记忆缺陷。这些结果表明NetB在MB肺叶扩展中具有关键作用,并确定NetB是FMRP的新靶标,有助于学习和记忆。电子补充材料本文的在线版本(10.1186 / s13041-019-0472-1)包含补充材料,可供授权用户使用。

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