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微小RNA介导的共生器官中宿主初始反应的调控

MicroRNA-Mediated Regulation of Initial Host Responses in a Symbiotic Organ.

作者信息

Moriano-Gutierrez Silvia, Ruby Edward G, McFall-Ngai Margaret J

机构信息

Pacific Biosciences Research Center, University of Hawai'i at Mānoa, Honolulu, Hawai'i, USA.

Pacific Biosciences Research Center, University of Hawai'i at Mānoa, Honolulu, Hawai'i, USA

出版信息

mSystems. 2021 May 11;6(3):e00081-21. doi: 10.1128/mSystems.00081-21.

Abstract

One of the most important events in an animal's life history is the initial colonization by its microbial symbionts, yet little is known about this event's immediate impacts on the extent of host gene expression or the molecular mechanisms controlling it. MicroRNAs (miRNAs) are short, noncoding RNAs that bind to target mRNAs, rapidly shaping gene expression by posttranscriptional control of mRNA translation and decay. Here, we show that, in the experimentally tractable binary squid-vibrio symbiosis, colonization of the light organ induces extensive changes in the miRNA transcriptome. Examination of the squid genome revealed the presence of evolutionarily conserved genes encoding elements essential for the production and processing of miRNAs. At 24 h postcolonization, 215 host miRNAs were detected in the light organ, 26 of which were differentially expressed in response to the symbionts. A functional enrichment analysis of genes potentially targeted by downregulation of certain miRNAs at the initiation of symbiosis revealed two major gene ontology (GO) term categories, neurodevelopment and tissue remodeling. This symbiont-induced downregulation is predicted to promote these activities in host tissues and is consistent with the well-described tissue remodeling that occurs at the onset of the association. Conversely, predicted targets of upregulated miRNAs, including the production of mucus, are consistent with attenuation of immune responses by symbiosis. Taken together, our data provide evidence that, at the onset of symbiosis, host miRNAs in the light organ drive alterations in gene expression that (i) orchestrate the symbiont-induced development of host tissues, and (ii) facilitate the partnership by dampening the immune response. Animals often acquire their microbiome from the environment at each generation, making the initial interaction of the partners a critical event in the establishment and development of a stable, healthy symbiosis. However, the molecular nature of these earliest interactions is generally difficult to study and poorly understood. We report that, during the initial 24 h of the squid-vibrio association, a differential expression of host miRNAs is triggered by the presence of the microbial partner. Predicted mRNA targets of these miRNAs were associated with regulatory networks that drive tissue remodeling and immune suppression, two major symbiosis-induced developmental outcomes in this and many other associations. These results implicate regulation by miRNAs as key to orchestrating the critical transcriptional responses that occur very early during the establishment of a symbiosis. Animals with more complex microbiota may have similar miRNA-driven responses as their association is initiated, supporting an evolutionary conservation of symbiosis-induced developmental mechanisms.

摘要

动物生命历程中最重要的事件之一是其微生物共生体的初始定殖,然而对于这一事件对宿主基因表达程度的直接影响或控制它的分子机制,我们却知之甚少。微小RNA(miRNA)是短的非编码RNA,可与靶标mRNA结合,通过对mRNA翻译和降解的转录后控制快速塑造基因表达。在此,我们表明,在实验上易于处理的鱿鱼-弧菌共生关系中,光器官的定殖会诱导miRNA转录组发生广泛变化。对鱿鱼基因组的研究揭示了存在编码miRNA产生和加工所必需元件的进化保守基因。在定殖后24小时,在光器官中检测到215种宿主miRNA,其中26种因共生体而差异表达。对共生开始时某些miRNA下调可能靶向的基因进行功能富集分析,揭示了两个主要的基因本体(GO)术语类别,即神经发育和组织重塑。这种共生体诱导的下调预计会促进宿主组织中的这些活动,并且与共生开始时发生的充分描述的组织重塑一致。相反,上调的miRNA的预测靶标,包括黏液的产生,与共生导致的免疫反应减弱一致。综上所述,我们的数据提供了证据,表明在共生开始时,光器官中的宿主miRNA驱动基因表达的改变,这些改变(i)协调共生体诱导的宿主组织发育,以及(ii)通过减弱免疫反应促进共生关系。动物通常在每一代都从环境中获得其微生物组,使得伙伴之间的初始相互作用成为建立和发展稳定、健康共生关系的关键事件。然而,这些最早相互作用的分子本质通常难以研究且了解甚少。我们报告称,在鱿鱼-弧菌共生关系的最初24小时内,微生物伙伴的存在触发了宿主miRNA的差异表达。这些miRNA的预测mRNA靶标与驱动组织重塑和免疫抑制的调控网络相关,这是这种以及许多其他共生关系中由共生诱导的两个主要发育结果。这些结果表明,miRNA调控是协调共生建立早期发生的关键转录反应的关键。随着共生关系的开始,具有更复杂微生物群的动物可能具有类似的由miRNA驱动的反应,这支持了共生诱导的发育机制的进化保守性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839f/8125070/5d188626ed12/mSystems.00081-21-f001.jpg

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