DNA Methylation Associates With Sex-Specific Effects of Experimentally Increased Yolk Testosterone in Wild Nestlings.

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Ecology Pub Date : 2025-02-01 Epub Date: 2025-01-06 DOI:10.1111/mec.17647
Bernice Sepers, Suvi Ruuskanen, Tjomme van Mastrigt, A Christa Mateman, Kees van Oers
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引用次数: 0

Abstract

Maternal hormones can profoundly impact offspring physiology and behaviour in sex-dependent ways. Yet little is known about the molecular mechanisms linking these maternal effects to offspring phenotypes. DNA methylation, an epigenetic mechanism, is suggested to facilitate maternal androgens' effects. To assess whether phenotypic changes induced by maternal androgens associate with DNA methylation changes, we experimentally manipulated yolk testosterone levels in wild great tit eggs (Parus major) and quantified phenotypic and DNA methylation changes in the hatched offspring. While we found no effect on the handing stress response, increased yolk testosterone levels decreased the begging probability, emphasised sex differences in fledging mass, and affected methylation at 763 CpG sites, but always in a sex-specific way. These sites are associated with genes involved in growth, oxidative stress, and reproduction, suggesting sex-specific trade-offs to balance the costs and benefits of exposure to high yolk testosterone levels. Future studies should assess if these effects extend beyond the nestling stage and impact fitness.

DNA甲基化与野生雏鸟卵黄睾酮实验增加的性别特异性效应相关。
母体荷尔蒙能以性别依赖的方式对后代的生理和行为产生深远影响。然而,人们对这些母体效应与后代表型之间的分子机制知之甚少。DNA甲基化是一种表观遗传机制,被认为能促进母体雄激素的作用。为了评估母体雄激素诱导的表型变化是否与DNA甲基化变化有关,我们通过实验操纵了野生大山雀卵中卵黄睾酮的水平,并量化了孵化后代的表型和DNA甲基化变化。我们发现,虽然卵黄睾酮水平的增加对交配应激反应没有影响,但却降低了乞食概率,强调了雏鸟质量的性别差异,并影响了763个CpG位点的甲基化,但总是以性别特异性的方式影响。这些位点与涉及生长、氧化应激和繁殖的基因有关,表明暴露于高卵黄睾酮水平的成本与收益之间存在性别特异性权衡。未来的研究应该评估这些影响是否会延伸到雏鸟阶段之后并影响其适应能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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