与微生物群描述符相关的植物遗传基础揭示了一种新的全生物通才基因理论。

IF 4.3 2区 生物学 Q2 MICROBIOLOGY
Loeiz Maillet, Manon Norest, Adam Kautsky, Anna Geraci, Elisabetta Oddo, Angelo Troia, Anne-Yvonne Guillerm-Erckelboudt, Cyril Falentin, Mathieu Rousseau-Gueutin, Anne-Marie Chèvre, Benjamin Istace, Corinne Cruaud, Caroline Belser, Jean-Marc Aury, Rosario Schicchi, Léa Frachon, Claudia Bartoli
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引用次数: 0

摘要

植物和动物一样,与一系列影响其健康、适应和进化的微生物有关。科学家把所有生物体都称为整体生物,即同时共同进化的复杂遗传单位。这就是最近提出的全基因组理论。这一激动人心的理论对动植物健康具有重要意义;然而,它仍然需要一致的证据来验证。事实上,全息生物在发生共同进化过程的自然栖息地的研究仍然很少。与动物相比,野生植物种群是探索全基因组理论的一个很好的模型。这些无根的整体生物已经与其微生物群共同进化了几十年,作用于野生植物的自然选择和适应过程可能调节植物与微生物的相互作用。本文对油菜(Brassica rapa) 26个天然居群进行了微生物群调查、植物基因组测序和基因组环境分析(GEA)。我们在意大利和法国收集了两个季节的植物,并分析了根和根际微生物群。在进行GEA时,我们证明了与真菌和细菌微生物群相关的整齐的峰值。令人惊讶的是,我们在真菌和细菌多样性描述符之间发现了13个共同基因,我们将其命名为全息生物通才基因(HGGs)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plant Genetic Bases Associated With Microbiota Descriptors Shed Light Into a Novel Holobiont Generalist Genes Theory

Plants as animals are associated with a cortege of microbes influencing their health, fitness and evolution. Scientists refer to all living organisms as holobionts, complex genetic units that coevolve simultaneously. This is what has been recently proposed as the hologenome theory. This exciting theory has important implications on animal and plant health; however, it still needs consistent proof to be validated. Indeed, holobionts are still poorly studied in their natural habitats where coevolution processes occur. Compared to animals, wild plant populations are an excellent model to explore the hologenome theory. These sessile holobionts have coevolved with their microbiota for decades, and natural selection and adaptive processes acting on wild plants are likely to regulate the plant–microbe interactions. Here, we conducted a microbiota survey, plant genome sequencing and genome–environmental analysis (GEA) of 26 natural populations of the plant species Brassica rapa. We collected plants over two seasons in Italy and France and analysed the root and rhizosphere microbiota. When conducting GEA, we evidenced neat peaks of association correlating with both fungal and bacterial microbiota. Surprisingly, we found 13 common genes between fungal and bacterial diversity descriptors that we referred to under the name of holobiont generalist genes (HGGs).

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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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