College of Life Sciences, State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Maoming, 525000, People's Republic of China.
Mar Biotechnol (NY). 2023 Feb;25(1):150-160. doi: 10.1007/s10126-022-10188-y. Epub 2022 Nov 29.
Fish suffer from starvation due to environmental risks such as extreme weather in the wild and due to insufficient feedings in farms. Nutrient problems from short-term or long-term starvation conditions can result in stress-related health problems for fish. Yellowfin seabream (Acanthopagrus latus) is an important marine economic fish in China. Understanding the molecular responses to starvation stress is vital for propagation and culturing yellowfin seabream. In this study, the transcriptome and genome-wide DNA methylation levels in the livers of yellowfin seabream under 14-days starvation stress were analyzed. One hundred sixty differentially expressed genes (DEGs) by RNA-Seq analysis and 737 differentially methylated-related genes by whole genome bisulfite sequencing analysis were identified. GO and KEGG pathway enrichment analysis found that energy metabolism-related pathways such as glucose metabolism and lipid metabolism were in response to starvation. Using bisulfite sequencing PCR, we confirmed the presence of CpG methylation differences within the regulatory region of a DEG ppargc1a in response to 14-days starvation stress. This study revealed the molecular responses of livers in response to starvation stress at the transcriptomic and whole genome DNA methylation levels in yellowfin seabream.
鱼类由于野外极端天气和养殖场投喂不足等环境风险而遭受饥饿,出现营养问题。短期或长期饥饿条件下的营养问题可能导致鱼类产生与应激相关的健康问题。黄鳍鲷(Acanthopagrus latus)是中国重要的海洋经济鱼类。了解其对饥饿应激的分子反应对于黄鳍鲷的繁殖和养殖至关重要。本研究分析了饥饿应激下黄鳍鲷肝脏的转录组和全基因组 DNA 甲基化水平。通过 RNA-Seq 分析鉴定了 160 个差异表达基因(DEGs),通过全基因组亚硫酸氢盐测序分析鉴定了 737 个差异甲基化相关基因。GO 和 KEGG 通路富集分析发现,葡萄糖代谢和脂质代谢等与能量代谢相关的途径对饥饿有反应。通过亚硫酸氢盐测序 PCR,我们证实了在 14 天饥饿应激下,DEG ppargc1a 的调控区域存在 CpG 甲基化差异。本研究揭示了黄鳍鲷肝脏在转录组和全基因组 DNA 甲基化水平上对饥饿应激的分子反应。