Université Paris-Saclay, INRAE, AgroParisTech, GABI, 78350, Jouy-en-Josas, France.
INRAE, SIGENAE, 78350, Jouy-en-Josas, France.
Epigenetics. 2021 Sep;16(9):1031-1052. doi: 10.1080/15592294.2020.1834924. Epub 2020 Oct 30.
Phenotypic plasticity is a key component of the ability of organisms to respond to changing environmental conditions. In this study, we aimed to study the establishment of DNA methylation marks in response to an environmental stress in rainbow trout and to assess whether these marks depend on the genetic background. The environmental stress chosen here was temperature, a known induction factor of epigenetic marks in fish. To disentangle the role of epigenetic mechanisms such as DNA methylation in generating phenotypic variations, nine rainbow trout isogenic lines with no genetic variability within a line were used. For each line, half of the eggs were incubated at standard temperature (11°C) and the other half at high temperature (16°C), from eyed-stage to hatching. In order to gain a first insight into the establishment of DNA methylation marks in response to an early temperature regime (control 11°C vs. heated 16°C), we have studied the expression of 8 (DNA methyltransferase) genes, potentially involved in methylation, and analysed global DNA methylation in the different rainbow trout isogenic lines using LUMA (LUminometric Methylation Assay). Finally, finer investigation of genome-wide methylation patterns was performed using EpiRADseq, a reduced-representation library approach based on the ddRADseq (Double Digest Restriction Associated DNA) protocol, for six rainbow trout isogenic lines. We have demonstrated that thermal history during embryonic development alters patterns of DNA methylation, but to a greater or lesser extent depending on the genetic background.
表型可塑性是生物体适应环境变化的关键组成部分。在这项研究中,我们旨在研究虹鳟鱼对环境胁迫建立 DNA 甲基化标记的情况,并评估这些标记是否依赖于遗传背景。这里选择的环境胁迫是温度,这是鱼类中已知的诱导表观遗传标记的因素。为了厘清如 DNA 甲基化等表观遗传机制在产生表型变异中的作用,我们使用了 9 个无遗传变异的虹鳟鱼同基因系。对于每条线,一半的卵在标准温度(11°C)下孵化,另一半在高温(16°C)下孵化,从眼期到孵化。为了初步了解早期温度条件(对照 11°C 与加热 16°C)下 DNA 甲基化标记的建立情况,我们研究了 8 个(DNA 甲基转移酶)基因的表达,这些基因可能参与了甲基化过程,并使用 LUMA(发光甲基化分析)分析了不同虹鳟鱼同基因系的全基因组 DNA 甲基化。最后,我们使用 EpiRADseq 对 6 个虹鳟鱼同基因系进行了全基因组甲基化模式的精细研究,EpiRADseq 是一种基于 ddRADseq(双酶切相关 DNA)方案的简化代表性文库方法。我们已经证明,胚胎发育过程中的热历史会改变 DNA 甲基化模式,但这种改变的程度因遗传背景而异。