Rapid Neural DNA Methylation Responses to Predation Stress in Trinidadian Guppies

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Janay A. Fox, Simon M. Reader, Rowan D. H. Barrett
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Abstract

DNA methylation (DNAm) is a well-studied epigenetic mechanism implicated in environmentally induced phenotypes and phenotypic plasticity. However, few studies investigate the timescale of DNAm shifts. Thus, it is uncertain whether DNAm can change on timescales relevant for rapid phenotypic shifts, such as during the expression of short-term behavioural plasticity. DNAm could be especially reactive in the brain, potentially increasing its relevance for behavioural plasticity. Most research investigating neural changes in methylation has been conducted in mammalian systems, on isolated individuals, and using stressors that are less ecologically relevant, reducing their generalisability to other natural systems. We exposed pairs of male and female Trinidadian guppies (Poecilia reticulata) to alarm cue, conspecific skin extract that reliably induces anti-predator behaviour, or a control cue. Whole-genome bisulphite sequencing on whole brains at various time points following cue exposure (0.5, 1, 4, 24, and 72 h) allowed us to uncover the timescale of neural DNAm responses. Males and females both showed rapid shifts in DNAm in as little as 0.5 h. However, males and females differed in the time course of their responses: both sexes showed a peak in the number of loci showing significant responses at 4 h, but males showed an additional peak at 72 h. We suggest that this finding could be due to the differing longer-term plastic responses between the sexes. This study shows that DNAm can be rapidly induced by an ecologically relevant stressor in fish and suggests that DNAm could be involved in short-term behavioural plasticity.

Abstract Image

特立尼达孔雀鱼对捕食压力的快速神经DNA甲基化反应
DNA甲基化(DNAm)是一种被广泛研究的表观遗传机制,与环境诱导的表型和表型可塑性有关。然而,很少有研究调查dna转移的时间尺度。因此,尚不确定DNAm是否会在与快速表型变化相关的时间尺度上发生变化,例如在短期行为可塑性的表达过程中。脱氧核糖核酸可能在大脑中特别活跃,潜在地增加了它与行为可塑性的相关性。大多数调查甲基化神经变化的研究都是在哺乳动物系统中进行的,在孤立的个体上进行的,并且使用了生态相关性较低的压力源,从而降低了它们在其他自然系统中的普遍性。我们将成对的雄性和雌性特立尼达孔雀鱼(Poecilia reticulata)暴露在警报提示、同种皮肤提取物(可靠地诱导反捕食者行为)或控制提示中。在线索暴露后的不同时间点(0.5、1、4、24和72小时)对全脑进行全基因组亚硫酸盐测序,使我们能够揭示神经dna反应的时间尺度。雄性和雌性在短短的0.5小时内都显示出dna的快速变化。然而,雄性和雌性在反应的时间过程上存在差异:两性在4小时时都出现了显著反应的位点数量高峰,但雄性在72小时时又出现了一个高峰。我们认为,这一发现可能是由于两性之间长期可塑性反应的不同。该研究表明,DNAm可以被生态相关的应激源快速诱导,并提示DNAm可能参与短期行为可塑性。
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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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