Multiomics Reveal Associations Between CpG Methylation, Histone Modifications and Transcription in a Species That has Lost DNMT3, the Colorado Potato Beetle.

IF 1.8 3区 生物学 Q3 DEVELOPMENTAL BIOLOGY
Zoe M Länger, Elisa Israel, Jan Engelhardt, Agata I Kalita, Claudia I Keller Valsecchi, Joachim Kurtz, Sonja J Prohaska
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引用次数: 0

Abstract

Insects display exceptional phenotypic plasticity, which can be mediated by epigenetic modifications, including CpG methylation and histone modifications. In vertebrates, both are interlinked and CpG methylation is associated with gene repression. However, little is known about these regulatory systems in invertebrates, where CpG methylation is mainly restricted to gene bodies of transcriptionally active genes. A widely conserved mechanism involves the co-transcriptional deposition of H3K36 trimethylation and the targeted methylation of unmethylated CpGs by the de novo DNA methyltransferase DNMT3. However, DNMT3 has been lost multiple times in invertebrate lineages raising the question of how the links between CpG methylation, histone modifications and gene expression are affected by its loss. Here, we report the epigenetic landscape of Leptinotarsa decemlineata, a beetle species that has lost DNMT3 but retained CpG methylation. We combine RNA-seq, enzymatic methyl-seq and CUT&Tag to study gene expression, CpG methylation and patterns of H3K36me3 and H3K27ac histone modifications on a genome-wide scale. Despite the loss of DNMT3, H3K36me3 mirrors CpG methylation patterns. Together, they give rise to signature profiles for expressed and not expressed genes. H3K27ac patterns show a prominent peak at the transcription start site that is predictive of expressed genes irrespective of their methylation status. Our study provides new insights into the evolutionary flexibility of epigenetic modification systems that urge caution when generalizing across species.

多组学揭示了丢失DNMT3的物种科罗拉多马铃薯甲虫CpG甲基化、组蛋白修饰和转录之间的关联。
昆虫表现出异常的表型可塑性,这可以通过表观遗传修饰介导,包括CpG甲基化和组蛋白修饰。在脊椎动物中,两者是相互关联的,CpG甲基化与基因抑制有关。然而,对无脊椎动物的这些调控系统知之甚少,其中CpG甲基化主要局限于转录活性基因的基因体。一个广泛保守的机制涉及H3K36三甲基化的共转录沉积和DNA甲基转移酶DNMT3对未甲基化CpGs的靶向甲基化。然而,DNMT3在无脊椎动物谱系中已经丢失多次,这就提出了CpG甲基化、组蛋白修饰和基因表达之间的联系如何受到其丢失的影响的问题。在这里,我们报告了Leptinotarsa decemlineata的表观遗传景观,这是一种失去DNMT3但保留CpG甲基化的甲虫物种。我们结合RNA-seq、酶促甲基化seq和CUT&Tag在全基因组范围内研究H3K36me3和H3K27ac组蛋白修饰的基因表达、CpG甲基化和模式。尽管DNMT3缺失,但H3K36me3反映了CpG甲基化模式。它们共同产生了表达和未表达基因的特征谱。H3K27ac模式在转录起始位点显示出一个显著的峰值,这是对表达基因的预测,无论其甲基化状态如何。我们的研究为表观遗传修饰系统的进化灵活性提供了新的见解,在跨物种推广时需要谨慎。
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来源期刊
CiteScore
4.80
自引率
9.10%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Developmental Evolution is a branch of evolutionary biology that integrates evidence and concepts from developmental biology, phylogenetics, comparative morphology, evolutionary genetics and increasingly also genomics, systems biology as well as synthetic biology to gain an understanding of the structure and evolution of organisms. The Journal of Experimental Zoology -B: Molecular and Developmental Evolution provides a forum where these fields are invited to bring together their insights to further a synthetic understanding of evolution from the molecular through the organismic level. Contributions from all these branches of science are welcome to JEZB. We particularly encourage submissions that apply the tools of genomics, as well as systems and synthetic biology to developmental evolution. At this time the impact of these emerging fields on developmental evolution has not been explored to its fullest extent and for this reason we are eager to foster the relationship of systems and synthetic biology with devo evo.
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