花蜜酵母对优先效应的转录反应

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Callie R Chappell, Pagé C Goddard, Lexi-Ann Golden, Jonathan Hernandez, Daniela Ortiz Chavez, Marziiah Hossine, Sur Herrera Paredes, Ethan VanValkenburg, Lucas A Nell, Tadashi Fukami, Manpreet K Dhami
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引用次数: 0

摘要

优先效应是指物种到达的顺序和时间会影响生态群落的组合。然而,优先效应的遗传和分子基础仍不清楚,这阻碍了人们更好地理解优先效应何时会变得强烈。我们的研究对象是蜂鸟授粉的 Diplacus (Mimulus) aurantiacus,我们试图对这种花蜜酵母 Metschnikowia reukaufii(常见于我们的研究植物--蜂鸟授粉的 Diplacus (Mimulus) aurantiacus--的花蜜中)获得这样的认识。在这种植物中,当 M. reukaufii 在其他花蜜酵母(如 M. rancensis)之后到达花朵时,会产生强烈的优先效应。在接种两种不同类型的合成花蜜以模拟 M. rancensis 提前到达后,我们对 108 株 M. reukaufii 进行了全转录组测序。我们发现,当花蜜经过 M. rancensis 的生长调节后,M. reukaufii 菌株中有几个基因的表达出现了差异。其中许多基因与氨基酸代谢有关,这表明M. reukaufii菌株对M. rancensis造成的氨基酸供应减少做出了分子反应。此外,对表达量性状位点(eQTLs)的调查显示,在 M. reukaufii 的某些基因变异中,涉及氨基酸转运和抗真菌化合物抗性的基因被富集。我们还发现,基因表达与种群增长率有关,尤其是在氨基酸有限的情况下。这些结果表明,花蜜酵母应对营养限制和直接真菌竞争的能力的种内遗传变异是这一微生物系统中优先效应的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptional Responses to Priority Effects in Nectar Yeast.

Priority effects, where the order and timing of species arrival influence the assembly of ecological communities, have been observed in a variety of taxa and habitats. However, the genetic and molecular basis of priority effects remains unclear, hindering a better understanding of when priority effects will be strong. We sought to gain such an understanding for the nectar yeast Metschnikowia reukaufii commonly found in the nectar of our study plant, the hummingbird-pollinated Diplacus (Mimulus) aurantiacus. In this plant, M. reukaufii can experience strong priority effects when it reaches flowers after other nectar yeasts, such as M. rancensis. After inoculation into two contrasting types of synthetic nectar simulating early arrival of M. rancensis, we conducted whole-transcriptome sequencing of 108 strains of M. reukaufii. We found that several genes were differentially expressed in M. reukaufii strains when the nectar had been conditioned by growth of M. rancensis. Many of these genes were associated with amino acid metabolism, suggesting that M. reukaufii strains responded molecularly to the reduction in amino acid availability caused by M. rancensis. Furthermore, investigation of expression quantitative trait loci (eQTLs) revealed that genes involved in amino acid transport and resistance to antifungal compounds were enriched in some genetic variants of M. reukaufii. We also found that gene expression was associated with population growth rate, particularly when amino acids were limited. These results suggest that intraspecific genetic variation in the ability of nectar yeasts to respond to nutrient limitation and direct fungal competition underpins priority effects in this microbial system.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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