Transition to Piscivory Seen Through Brain Transcriptomics in a Juvenile Percid Fish: Complex Interplay of Differential Gene Transcription, Alternative Splicing, and ncRNA Activity

Radka Symonová, Tomáš Jůza, Million Tesfaye, Marek Brabec, Daniel Bartoň, Petr Blabolil, Vladislav Draštík, Luboš Kočvara, Milan Muška, Marie Prchalová, Milan Říha, Marek Šmejkal, Allan T. Souza, Zuzana Sajdlová, Michal Tušer, Mojmír Vašek, Cene Skubic, Jakub Brabec, Jan Kubečka
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Abstract

Pikeperch (Sander Lucioperca) belongs to main predatory fish species in freshwater bodies throughout Europe playing the key role by reducing planktivorous fish abundance. Two size classes of the young-of-the-year (YOY) pikeperch are known in Europe and North America. Our long-term fish survey elucidates late-summer size distribution of YOY pikeperch in the Lipno Reservoir (Czechia) and recognizes two distinct subcohorts: smaller pelagic planktivores heavily outnumber larger demersal piscivores. To explore molecular mechanisms accompanying the switch from planktivory to piscivory, we compared brain transcriptomes of both subcohorts and identified 148 differentially transcribed genes. The pathway enrichment analyses identified the piscivorous phase to be associated with genes involved in collagen and extracellular matrix generation with numerous Gene Ontology (GO), while the planktivorous phase was associated with genes for non-muscle-myosins (NMM) with less GO terms. Transcripts further upregulated in planktivores from the periphery of the NMM network were Pmchl, Pomcl, and Pyyb, all involved also in appetite control and producing (an)orexigenic neuropeptides. Noncoding RNAs were upregulated in transcriptomes of planktivores including three transcripts of snoRNA U85. Thirty genes mostly functionally unrelated to those differentially transcribed were alternatively spliced between the subcohorts. Our results indicate planktivores as potentially driven by voracity to initiate the switch to piscivory, while piscivores undergo a dynamic brain development. We propose a spatiotemporal spreading of juvenile development over a longer period and larger spatial scales through developmental plasticity as an adaptation to exploiting all types of resources and decreasing the intraspecific competition.

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通过幼鱼脑转录组学观察向鱼科鱼类的转变:差异基因转录、选择性剪接和ncRNA活性的复杂相互作用。
刺鲈(Sander Lucioperca)是欧洲淡水水体中主要的掠食性鱼类,在减少浮游鱼类丰度方面起着关键作用。在欧洲和北美,有两种年龄最小(YOY)的棘鲈。我们的长期鱼类调查阐明了利普诺水库(捷克)YOY梭鲈的夏末尺寸分布,并识别出两个不同的亚群:较小的上层浮游动物数量远远超过较大的底栖鱼类。为了探索浮游生物向鱼类转变的分子机制,我们比较了两个亚群的脑转录组,并鉴定了148个差异转录基因。途径富集分析发现,鱼食性阶段与胶原蛋白和细胞外基质生成相关的基因具有大量的基因本体(GO),而浮游食性阶段与非肌肉肌球蛋白(NMM)相关的基因具有较少的GO项。在浮游动物中,NMM网络外围进一步上调的转录本是Pmchl、Pomcl和Pyyb,它们也参与食欲控制和产生(和)摄氧神经肽。浮游动物转录组中的非编码rna上调,其中包括三个snoRNA U85转录本。在亚群之间选择性地拼接了30个与差异转录基因在功能上大多无关的基因。我们的研究结果表明,浮游动物可能是在贪婪的驱使下开始向鱼类转变的,而鱼类则经历了一个动态的大脑发育过程。我们认为,幼体发育通过发育可塑性在更长的时间和更大的空间尺度上进行时空扩展,以适应开发各种类型的资源和减少种内竞争。
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来源期刊
Journal of experimental zoology. Part A, Ecological and integrative physiology
Journal of experimental zoology. Part A, Ecological and integrative physiology Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
4.90
自引率
3.60%
发文量
0
期刊介绍: The Journal of Experimental Zoology – A publishes articles at the interface between Development, Physiology, Ecology and Evolution. Contributions that help to reveal how molecular, functional and ecological variation relate to one another are particularly welcome. The Journal publishes original research in the form of rapid communications or regular research articles, as well as perspectives and reviews on topics pertaining to the scope of the Journal. Acceptable articles are limited to studies on animals.
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