Dynamic changes in DNA methylation during seahorse (Hippocampus reidi) postnatal development and settlement.

IF 2.6 2区 生物学 Q1 ZOOLOGY Frontiers in Zoology Pub Date : 2021-10-09 DOI:10.1186/s12983-021-00436-7
Paula Suarez-Bregua, Sofia Rosendo, Pilar Comesaña, Lucia Sánchez-Ruiloba, Paloma Morán, Miquel Planas, Josep Rotllant
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引用次数: 4

Abstract

Introduction: Most living marine organisms have a biphasic life cycle dependent on metamorphosis and settlement. These critical life-history events mean that a developmentally competent larva undergoes a range of coordinated morphological and physiological changes that are in synchrony with the ecological transition from a pelagic to a benthonic lifestyle. Therefore, transition from a pelagic to a benthonic habitat requires multiple adaptations, however, the underlying mechanisms regulating this process still remains unclear. Epigenetic regulation and specifically DNA methylation, has been suggested to be particularly important for organisms to adapt to new environments. Seahorses (Family Syngnathidae, Genus Hippocampus) are a fascinating group of fish, distinguished by their unique anatomical features, reproductive strategy and behavior. They are unique among vertebrate species due to their "male pregnancy", where males nourish developing embryos and larvae in a brood pouch until hatching and parturition occurs. After birth, free-swimming offspring are pelagic and subsequently they change into a demersal lifestyle. Therefore, to begin to address the question whether epigenetic processes could be involved in the transition from a planktonic to a benthonic lifestyle observed in seahorses, we studied global DNA methylation profiles in a tropical seahorse species (Hippocampus reidi) during postnatal development and settlement.

Results: We performed methylation-sensitive amplified polymorphism (MSAP) along with quantitative expression analysis for genes suggested to be involved in the methylation machinery at six age groups: 1, 5, 10, 20, 30 and 40 days after male's pouch release (DAR). Results revealed that the H. reidi genome has a significantly different DNA methylation profile during postnatal development and settlement on demersal habitats. Moreover, gene expression analysis showed up- and down-regulation of specific DNA methyltransferases (DNMTs) encoding genes.

Conclusion: Our data show that the differences in the DNA methylation patterns seen among developmental stages and during the transition from a pelagic to a benthonic lifestyle suggest a potential for epigenetic regulation of gene expression (through DNA methylation) in this species. Therefore, epigenetic mechanisms could be necessary for seahorse settlement. Nevertheless, if these epigenetic mechanisms come from internal or if they are initiated via external environmental cues should be further investigated.

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海马出生后发育和定居过程中DNA甲基化的动态变化。
大多数海洋生物都有一个依赖于变态和定居的双阶段生命周期。这些关键的生活史事件意味着,具有发育能力的幼虫经历了一系列协调的形态和生理变化,这些变化与从远洋生活方式向底栖生活方式的生态转变是同步的。因此,从远洋生境到底栖生境的转变需要多种适应,然而,调节这一过程的潜在机制仍不清楚。表观遗传调控,特别是DNA甲基化,被认为对生物体适应新环境特别重要。海马(海马科,海马属)是一种迷人的鱼类,以其独特的解剖特征、繁殖策略和行为而闻名。它们在脊椎动物物种中是独一无二的,因为它们的“雄性怀孕”,雄性在育儿袋中滋养发育中的胚胎和幼虫,直到孵化和分娩。出生后,自由游泳的后代是远洋动物,随后它们转变为海底生活方式。因此,为了开始解决表观遗传过程是否可能参与海马从浮游到底栖生活方式的转变,我们研究了一个热带海马物种(海马reidi)在出生后发育和定居期间的全球DNA甲基化谱。结果:我们对6个年龄组(雄性育儿袋释放后1、5、10、20、30和40天)的甲基化机制相关基因进行了甲基化敏感扩增多态性(MSAP)和定量表达分析。结果表明,雷地人在出生后发育和在地下栖息地定居期间,基因组的DNA甲基化谱存在显著差异。此外,基因表达分析显示特异性DNA甲基转移酶(dnmt)编码基因的上调和下调。结论:我们的数据表明,在发育阶段和从远洋生活方式到底栖生活方式的转变过程中,DNA甲基化模式的差异表明,该物种可能存在基因表达的表观遗传调控(通过DNA甲基化)。因此,海马定居的表观遗传机制可能是必要的。然而,这些表观遗传机制是来自内部还是通过外部环境线索启动的,应该进一步研究。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Frontiers in Zoology is an open access, peer-reviewed online journal publishing high quality research articles and reviews on all aspects of animal life. As a biological discipline, zoology has one of the longest histories. Today it occasionally appears as though, due to the rapid expansion of life sciences, zoology has been replaced by more or less independent sub-disciplines amongst which exchange is often sparse. However, the recent advance of molecular methodology into "classical" fields of biology, and the development of theories that can explain phenomena on different levels of organisation, has led to a re-integration of zoological disciplines promoting a broader than usual approach to zoological questions. Zoology has re-emerged as an integrative discipline encompassing the most diverse aspects of animal life, from the level of the gene to the level of the ecosystem. Frontiers in Zoology is the first open access journal focusing on zoology as a whole. It aims to represent and re-unite the various disciplines that look at animal life from different perspectives and at providing the basis for a comprehensive understanding of zoological phenomena on all levels of analysis. Frontiers in Zoology provides a unique opportunity to publish high quality research and reviews on zoological issues that will be internationally accessible to any reader at no cost. The journal was initiated and is supported by the Deutsche Zoologische Gesellschaft, one of the largest national zoological societies with more than a century-long tradition in promoting high-level zoological research.
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