Transcriptome-wide methylated RNA immunoprecipitation sequencing profiling reveals m6A modification involved in response to heat stress in Apostichopus japonicus.

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yanan Sun, Youmei Sun, Xiaohua He, Siyi Li, Xiaohui Xu, Yanwei Feng, Jianmin Yang, Rubiao Xie, Guohua Sun
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引用次数: 0

Abstract

Background: Global warming-induced environmental stresses have diverse effects on gene expression and regulation in the life processes of various aquatic organisms. N6 adenylate methylation (m6A) modifications are known to influence mRNA transcription, localization, translation, stability, splicing, and nuclear export, which are pivotal in mediating stress responses. Apostichopus japonicus is a significant species in aquaculture and a representative of benthic organisms in ecosystems, thus there is a growing need for research on its heat stress mechanism.

Results: In this study, m6A-modified whole transcriptome profiles of the respiratory tree tissues of A. japonicus in the control (T18) and high-temperature stress (T32) groups were obtained using MeRIP-seq technology. The results showed that 7,211 common m6A peaks, and 9,459 genes containing common m6A were identified in three replicates T18 and T32 groups. The m6A peaks were found to be highly enriched in the 3' untranslated region, and the common sequence of the m6A peak was also enriched, which was shown as RRACH (R = G or A; H = A, C, or U). A total of 1,200 peaks were identified as significantly differentially enriched in the T32 group compared with the T18 group. Among them, 245 peaks were upregulated and 955 were downregulated, which indicated that high temperature stress significantly altered the methylation pattern of m6A, and there were more demethylation sites in the T32 group. Conjoint analysis of the m6A methylation modification and the transcript expression level (the MeRIP-seq and RNA-seq data) showed co-differentiated 395 genes were identified, which were subsequently divided into four groups with a predominant pattern that more genes with decreased m6A modification and up-regulated expression, including HSP70IV, EIF2AK1, etc. GO enrichment and KEGG analyses of differential m6A peak related genes and co-differentiated genes showed the genes were significantly associated with transcription process and pathways such as protein processing in the endoplasmic reticulum, Wnt signaling pathway, and mTOR signaling pathway, etc. CONCLUSION: The comparisons of m6A modification patterns and conjoint analyses of m6A modification and gene expression profiles suggest that m6A modification was involved in the regulation of heat stress-responsive genes and important functional pathways in A. japonicus in response to high-temperature stress. The study will contribute to elucidate the regulatory mechanism of m6A modification in the response of A. japonicus to environmental stress, as well as the conservation and utilization of sea cucumber resources in the context of environmental changes.

全转录组甲基化 RNA 免疫沉淀测序分析揭示了日本狎鸥鸥对热胁迫反应中涉及的 m6A 修饰。
背景:全球变暖引起的环境胁迫对各种水生生物生命过程中的基因表达和调控产生了不同的影响。众所周知,N6腺苷酸甲基化(m6A)修饰可影响mRNA的转录、定位、翻译、稳定性、剪接和核输出,在介导应激反应中起着关键作用。日本芹菜是水产养殖中的重要物种,也是生态系统中底栖生物的代表,因此对其热应激机制的研究需求越来越大:结果:本研究利用 MeRIP-seq 技术获得了对照组(T18)和高温胁迫组(T32)日本竹节虫呼吸树组织的 m6A修饰全转录组图谱。结果表明,在三个重复的 T18 和 T32 组中,共鉴定出 7,211 个常见 m6A 峰和 9,459 个含有常见 m6A 的基因。结果发现,m6A峰高度富集于3'非翻译区,m6A峰的共同序列也被富集,显示为RRACH(R = G或A;H = A、C或U)。与 T18 组相比,共有 1,200 个峰在 T32 组中明显富集。其中,245个峰上调,955个峰下调,这表明高温胁迫明显改变了m6A的甲基化模式,T32组的去甲基化位点较多。对m6A甲基化修饰和转录表达水平(MeRIP-seq和RNA-seq数据)的联合分析表明,共发现了395个共同分化的基因,随后将其分为4组,主要模式是m6A修饰减少而表达上调的基因较多,包括HSP70IV、EIF2AK1等。对差异m6A峰相关基因和共分化基因的GO富集和KEGG分析表明,这些基因与内质网蛋白加工、Wnt信号通路、mTOR信号通路等转录过程和通路显著相关。结论:m6A修饰模式的比较以及m6A修饰和基因表达谱的联合分析表明,m6A修饰参与了日本箭毒对高温胁迫响应基因和重要功能通路的调控。该研究将有助于阐明m6A修饰在日本刺参对环境胁迫响应中的调控机制,以及环境变化背景下海参资源的保护和利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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