Changes in Genome-Wide Methylation and Gene Expression in Response to Future pCO2 Extremes in the Antarctic Pteropod Limacina helicina antarctica
Changes in Genome-Wide Methylation and Gene Expression in Response to Future pCO2 Extremes in the Antarctic Pteropod Limacina helicina antarctica
复制标题
南极翼足类Limacina helicina anarctica全基因组甲基化和基因表达对未来极端pCO2的响应变化
DOI:
10.3389/fmars.2019.00788
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发表时间:
2020-01-22
影响因子:
3.7
通讯作者:
Hofmann, Gretchen E.
中科院分区:
文献类型:
--
作者:
Bogan, Samuel N.;Johnson, Kevin M.;Hofmann, Gretchen E.
Epigenetic processes such as variation in DNA methylation may promote phenotypic plasticity and the rapid acclimatization of species to environmental change. The extent to which an organism can mount an epigenetic response to current and future climate extremes may influence its capacity to acclimatize or adapt to global change on ecological rather than evolutionary time scales. The thecosome pteropod Limacina helicina antarctica is an abundant macrozooplankton endemic to the Southern Ocean and is considered a bellwether of ocean acidification as it is highly sensitive to variation in carbonate chemistry. In this study, we quantified variation in DNA methylation and gene expression over time across different ocean acidification regimes. We exposed L. helicina antarctica to pCO(2) levels mimicking present-day norms in the coastal Southern Ocean of 255 matm pCO(2), present-day extremes of 530 matm pCO(2), and projected extremes of 918 matm pCO(2) for up to 7 days before measuring global DNA methylation and sequencing transcriptomes in animals from each treatment across time. L. helicina antarctica significantly reduced DNA methylation by 29-56% after 1 day of exposure to 918 matm pCO(2) before DNA methylation returned to control levels after 6 days. In addition, L. helicina antarctica exposed to 918 matm pCO(2) exhibited drastically more differential expression compared to cultures replicating present-day pCO(2) extremes. Differentially expressed transcripts were predominantly downregulated. Furthermore, downregulated genes were enriched with signatures of gene body methylation. These findings support the potential role of DNA methylation in regulating transcriptomic responses by L. helicina antarctica to future ocean acidification and in situ variation in pCO(2) experienced seasonally or during vertical migration. More broadly, L. helicina antarctica was capable of mounting a substantial epigenetic response to ocean acidification despite little evidence of metabolic compensation or recovery of the cellular stress response in this species at future pCO(2) levels.