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Whole-Genome DNA Methylation Profile of the Jewel Wasp (Nasonia vitripennis)

机译:黄蜂(Nasonia vitripennis)的全基因组DNA甲基化分布

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摘要

The epigenetic mark of DNA methylation, the addition of a methyl (CH3) group to a cytosine residue, has been extensively studied in many mammalian genomes and, although it is commonly found at the promoter regions of genes, it is also involved in a number of different biological functions. In other complex animals, such as social insects, DNA methylation has been determined to be involved in caste differentiation and to occur primarily in gene bodies. The role of methylation in nonsocial insects, however, has not yet been explored thoroughly. Here, we present the whole-genome DNA methylation profile of the nonsocial hymenopteran, the jewel wasp (Nasonia vitripennis). From high-throughput sequencing of bisulfite-converted gDNA extracted from male Nasonia thoraces, we were able to determine which cytosine residues are methylated in the entire genome. We found that an overwhelming majority of methylated sites (99.7%) occur at cytosines followed by a guanine in the 3′ direction (CpG sites). Additionally, we found that a majority of methylation in Nasonia occurs within exonic regions of the genome (more than 62%). Overall, methylation is sparse in Nasonia, occurring only at 0.18% of all sites and at 0.63% of CpGs. Our analysis of the Nasonia methylome revealed that in contrast to the methylation profile typically seen in mammals, methylation is sparse and is constrained primarily to exons. This methylation profile is more similar to that of the social hymenopteran species, the honey bee (Apis mellifera). In presenting the Nasonia methylome, we hope to promote future investigation of the regulatory function of DNA methylation in both social and nonsocial hymenoptera.
机译:DNA甲基化的表观遗传标记(向胞嘧啶残基添加甲基(CH3)基团)已在许多哺乳动物基因组中进行了广泛研究,尽管通常在基因的启动子区域发现,但它也涉及许多不同的生物学功能。在其他复杂的动物(例如社交昆虫)中,DNA甲基化已被确定参与种姓分化并主要发生在基因体中。然而,甲基化在非社会性昆虫中的作用尚未得到充分研究。在这里,我们介绍了非社会膜翅类动物,黄蜂(Nasonia vitripennis)的全基因组DNA甲基化谱。通过从雄性纳索尼亚胸衣提取的亚硫酸氢盐转化的gDNA的高通量测序,我们能够确定整个基因组中哪些胞嘧啶残基被甲基化。我们发现绝大多数的甲基化位点(99.7%)出现在胞嘧啶上,随后是鸟嘌呤在3'方向(CpG位点)。此外,我们发现纳索尼亚的大部分甲基化发生在基因组的外显子区域内(超过62%)。总体而言,纳沙尼亚甲基化稀疏,仅发生在所有位点的0.18%和CpG的0.63%。我们对纳索尼亚(Nasonia)甲基化基因组的分析表明,与通常在哺乳动物中看到的甲基化谱相反,甲基化是稀疏的,并且主要局限于外显子。这种甲基化特征更类似于社交膜翅目蜜蜂(蜜蜂)的甲基化特征。在介绍Nasonia甲基化组时,我们希望促进将来对社交和非社交膜翅目中DNA甲基化调节功能的研究。

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