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microRNA 维持共生体-宿主相互作用中的营养稳态。

microRNA maintains nutrient homeostasis in the symbiont-host interaction.

机构信息

Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400715, China.

Key Laboratory of Agricultural Biosafety and Green Production of Upper Yangtze River (Ministry of Education), Academy of Agricultural Sciences, Southwest University, Chongqing 400715, China.

出版信息

Proc Natl Acad Sci U S A. 2024 Sep 3;121(36):e2406925121. doi: 10.1073/pnas.2406925121. Epub 2024 Aug 28.

DOI:10.1073/pnas.2406925121
PMID:39196627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11388328/
Abstract

Endosymbionts provide essential nutrients for hosts, promoting growth, development, and reproduction. However, the molecular regulation of nutrient transport from endosymbiont to host is not well understood. Here, we used bioinformatic analysis, RNA-Sequencing, luciferase assays, RNA immunoprecipitation, and in situ hybridization to show that a bacteriocyte-distributed gene (multidrug resistance-associated protein 4) is negatively regulated by a host (aphid)-specific microRNA (miR-3024). Targeted metabolomics, microbiome analysis, vitamin B6 (VB6) supplements, 3D modeling/molecular docking, in vitro binding assays (voltage clamp recording and microscale thermophoresis), and functional complementation of were jointly used to show that the miR-3024/ axis controls endosymbiont ()-produced VB6 transport to the host. The supplementation of miR-3024 increased the mortality of aphids, but partial rescue was achieved by providing an external source of VB6. The use of miR-3024 as part of a sustainable aphid pest-control strategy was evaluated by safety assessments in nontarget organisms (pollinators, predators, and entomopathogenic fungi) using virus-induced gene silencing assays and the expression of miR-3024 in transgenic tobacco. The supplementation of miR-3024 suppresses expression, restricting the number of membrane channels, inhibiting VB6 transport, and ultimately killing the host. Under aphids facing stress conditions, the endosymbiont titer is decreased, and the VB6 production is also down-regulated, while the aphid's autonomous inhibition of miR-3024 enhances the expression of and then increases the VB6 transport which finally ensures the VB6 homeostasis. The results confirm that miR-3024 regulates nutrient transport in the endosymbiont-host system and is a suitable target for sustainable pest control.

摘要

共生体为宿主提供必需的营养物质,促进生长、发育和繁殖。然而,共生体向宿主传输营养物质的分子调控机制尚不清楚。在这里,我们使用生物信息学分析、RNA 测序、荧光素酶测定、RNA 免疫沉淀和原位杂交表明,一种菌细胞分布的基因(多药耐药相关蛋白 4)受宿主(蚜虫)特异性 microRNA(miR-3024)负调控。靶向代谢组学、微生物组分析、维生素 B6(VB6)补充剂、3D 建模/分子对接、体外结合测定(电压钳记录和微尺度热泳)以及的功能互补共同表明,miR-3024/轴控制共生体()产生的 VB6 向宿主的转运。miR-3024 的补充增加了蚜虫的死亡率,但通过提供 VB6 的外源性来源可以部分挽救。使用 miR-3024 作为可持续蚜虫防治策略的一部分,通过病毒诱导基因沉默测定和转烟草中 miR-3024 的表达,在非靶标生物(传粉者、捕食者和昆虫病原真菌)中进行了安全性评估。miR-3024 的补充抑制了的表达,限制了膜通道的数量,抑制了 VB6 的转运,最终导致宿主死亡。在面临压力条件的蚜虫中,共生体滴度降低,VB6 产量也下调,而蚜虫自主抑制 miR-3024 增强了的表达,从而增加了 VB6 的转运,最终确保了 VB6 的体内平衡。研究结果证实,miR-3024 调节共生体-宿主系统中的营养物质运输,是可持续害虫控制的合适靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/6cd837b7db7a/pnas.2406925121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/40846f7c55b7/pnas.2406925121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/d3603e6a4826/pnas.2406925121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/cfafbb315b1e/pnas.2406925121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/d8fa95a8221a/pnas.2406925121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/256dca2aaa1c/pnas.2406925121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/6cd837b7db7a/pnas.2406925121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/40846f7c55b7/pnas.2406925121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/d3603e6a4826/pnas.2406925121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/cfafbb315b1e/pnas.2406925121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/d8fa95a8221a/pnas.2406925121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/256dca2aaa1c/pnas.2406925121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8877/11388328/6cd837b7db7a/pnas.2406925121fig06.jpg

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