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蜜蜂转录组的表观遗传调控:揭示甲基化基因的本质

Epigenetic regulation of the honey bee transcriptome: unravelling the nature of methylated genes.

作者信息

Foret Sylvain, Kucharski Robert, Pittelkow Yvonne, Lockett Gabrielle A, Maleszka Ryszard

机构信息

Centre for Bioinformation, Mathematical Sciences Institute, The Australian National University, Canberra ACT 0200, Australia.

出版信息

BMC Genomics. 2009 Oct 14;10:472. doi: 10.1186/1471-2164-10-472.

Abstract

BACKGROUND

Epigenetic modification of DNA via methylation is one of the key inventions in eukaryotic evolution. It provides a source for the switching of gene activities, the maintenance of stable phenotypes and the integration of environmental and genomic signals. Although this process is widespread among eukaryotes, both the patterns of methylation and their relevant biological roles not only vary noticeably in different lineages, but often are poorly understood. In addition, the evolutionary origins of DNA methylation in multicellular organisms remain enigmatic. Here we used a new 'epigenetic' model, the social honey bee Apis mellifera, to gain insights into the significance of methylated genes.

RESULTS

We combined microarray profiling of several tissues with genome-scale bioinformatics and bisulfite sequencing of selected genes to study the honey bee methylome. We find that around 35% of the annotated honey bee genes are expected to be methylated at the CpG dinucleotides by a highly conserved DNA methylation system. We show that one unifying feature of the methylated genes in this species is their broad pattern of expression and the associated 'housekeeping' roles. In contrast, genes involved in more stringently regulated spatial or temporal functions are predicted to be un-methylated.

CONCLUSION

Our data suggest that honey bees use CpG methylation of intragenic regions as an epigenetic mechanism to control the levels of activity of the genes that are broadly expressed and might be needed for conserved core biological processes in virtually every type of cell. We discuss the implications of our findings for genome-scale regulatory network structures and the evolution of the role(s) of DNA methylation in eukaryotes. Our findings are particularly important in the context of the emerging evidence that environmental factors can influence the epigenetic settings of some genes and lead to serious metabolic and behavioural disorders.

摘要

背景

DNA通过甲基化进行的表观遗传修饰是真核生物进化中的关键创新之一。它为基因活性的转换、稳定表型的维持以及环境与基因组信号的整合提供了一个来源。尽管这一过程在真核生物中广泛存在,但甲基化模式及其相关生物学作用不仅在不同谱系中显著不同,而且通常了解甚少。此外,多细胞生物中DNA甲基化的进化起源仍然是个谜。在此,我们使用一种新的“表观遗传”模型——群居蜜蜂(意大利蜜蜂)来深入了解甲基化基因的重要性。

结果

我们将多个组织的微阵列分析与全基因组规模的生物信息学以及选定基因的亚硫酸氢盐测序相结合,以研究蜜蜂的甲基化组。我们发现,通过一个高度保守的DNA甲基化系统,预计约35%的已注释蜜蜂基因在CpG二核苷酸处会发生甲基化。我们表明,该物种中甲基化基因的一个统一特征是其广泛的表达模式以及相关的“管家”功能。相比之下,参与更严格调控的空间或时间功能的基因预计是未甲基化的。

结论

我们的数据表明,蜜蜂利用基因内区域的CpG甲基化作为一种表观遗传机制,来控制广泛表达且可能在几乎每种类型细胞的保守核心生物学过程中都需要的基因的活性水平。我们讨论了我们的发现对基因组规模调控网络结构以及真核生物中DNA甲基化作用进化的影响。鉴于新出现的证据表明环境因素可影响某些基因的表观遗传状态并导致严重的代谢和行为障碍,我们的发现尤为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc1/2768749/f4d15fe969af/1471-2164-10-472-1.jpg

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