Länger Zoe M, Israel Elisa, Engelhardt Jan, Kalita Agata I, Keller Valsecchi Claudia I, Kurtz Joachim, Prohaska Sonja J
Institute for Evolution and Biodiversity (IEB), University of Münster, Münster, Germany.
Computational EvoDevo Group, Institute of Computer Science, Leipzig University, Leipzig, Germany.
J Exp Zool B Mol Dev Evol. 2025 May 12. doi: 10.1002/jez.b.23303.
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.
昆虫表现出非凡的表型可塑性,这可由表观遗传修饰介导,包括CpG甲基化和组蛋白修饰。在脊椎动物中,两者相互关联,且CpG甲基化与基因抑制相关。然而,对于无脊椎动物中的这些调控系统我们知之甚少,在无脊椎动物中,CpG甲基化主要局限于转录活跃基因的基因体。一种广泛保守的机制涉及H3K36三甲基化的共转录沉积以及从头DNA甲基转移酶DNMT3对未甲基化CpG的靶向甲基化。然而,DNMT3在无脊椎动物谱系中多次丢失,这就引发了一个问题,即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。在这里,我们报告了马铃薯甲虫的表观遗传图谱,这是一种已经丢失DNMT3但保留了CpG甲基化的甲虫物种。我们结合RNA测序、酶促甲基测序和切割与标签技术,在全基因组范围内研究基因表达、CpG甲基化以及H3K36me3和H3K27ac组蛋白修饰模式。尽管DNMT3丢失,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图谱。H3K27ac模式在转录起始位点显示出一个突出的峰值,无论基因的甲基化状态如何,该峰值都可预测表达的基因。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,这促使我们在跨物种进行概括时要谨慎。