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秀丽隐杆线虫基因组中的 5-甲基胞嘧啶和 5-羟甲基胞嘧啶。

5-methyl-cytosine and 5-hydroxy-methyl-cytosine in the genome of Biomphalaria glabrata, a snail intermediate host of Schistosoma mansoni.

机构信息

Université de Perpignan Via Domitia, Perpignan, France.

出版信息

Parasit Vectors. 2013 Jun 6;6:167. doi: 10.1186/1756-3305-6-167.

Abstract

BACKGROUND

Biomphalaria glabrata is the mollusc intermediate host for Schistosoma mansoni, a digenean flatworm parasite that causes human intestinal schistosomiasis. An estimated 200 million people in 74 countries suffer from schistosomiasis, in terms of morbidity this is the most severe tropical disease after malaria. Epigenetic information informs on the status of gene activity that is heritable, for which changes are reversible and that is not based on the DNA sequence. Epigenetic mechanisms generate variability that provides a source for potentially heritable phenotypic variation and therefore could be involved in the adaptation to environmental constraint. Phenotypic variations are particularly important in host-parasite interactions in which both selective pressure and rate of evolution are high. In this context, epigenetic changes are expected to be major drivers of phenotypic plasticity and co-adaptation between host and parasite. Consequently, with characterization of the genomes of invertebrates that are parasite vectors or intermediate hosts, it is also essential to understand how the epigenetic machinery functions to better decipher the interplay between host and parasite.

METHODS

The CpGo/e ratios were used as a proxy to investigate the occurrence of CpG methylation in B. glabrata coding regions. The presence of DNA methylation in B. glabrata was also confirmed by several experimental approaches: restriction enzymatic digestion with isoschizomers, bisulfite conversion based techniques and LC-MS/MS analysis.

RESULTS

In this work, we report that DNA methylation, which is one of the carriers of epigenetic information, occurs in B. glabrata; approximately 2% of cytosine nucleotides are methylated. We describe the methylation machinery of B. glabrata. Methylation occurs predominantly at CpG sites, present at high ratios in coding regions of genes associated with housekeeping functions. We also demonstrate by bisulfite treatment that methylation occurs in multiple copies of Nimbus, a transposable element.

CONCLUSIONS

This study details DNA methylation for the first time, one of the carriers of epigenetic information in B. glabrata. The general characteristics of DNA methylation that we observed in the B. glabrata genome conform to what epigenetic studies have reported from other invertebrate species.

摘要

背景

光滑双脐螺是曼氏血吸虫的中间宿主软体动物,曼氏血吸虫是一种寄生扁形吸虫,会导致人类肠道血吸虫病。据估计,全球有 74 个国家的 2 亿多人患有血吸虫病,就发病率而言,这是继疟疾之后最严重的热带病。表观遗传信息提供了可遗传的基因活性状态信息,其变化是可逆的,且不基于 DNA 序列。表观遗传机制产生了可提供潜在遗传表型变异来源的变异性,因此可能参与了对环境约束的适应。表型变异在宿主-寄生虫相互作用中尤为重要,因为在这种相互作用中,选择压力和进化速度都很高。在这种情况下,预计表观遗传变化将是宿主-寄生虫之间表型可塑性和共同适应的主要驱动因素。因此,随着寄生虫载体或中间宿主无脊椎动物基因组的特征描述,了解表观遗传机制的功能对于更好地破译宿主与寄生虫之间的相互作用也至关重要。

方法

CpGo/e 比值被用作研究光滑双脐螺编码区 CpG 甲基化发生的替代指标。通过几种实验方法也证实了双脐螺中存在 DNA 甲基化:使用同裂酶进行限制性酶切消化、基于亚硫酸氢盐转化的技术和 LC-MS/MS 分析。

结果

在这项工作中,我们报告了 DNA 甲基化(一种表观遗传信息的载体)发生在双脐螺中;大约 2%的胞嘧啶核苷酸被甲基化。我们描述了双脐螺的甲基化机制。甲基化主要发生在与管家功能相关的基因的编码区中 CpG 位点较高的比率。我们还通过亚硫酸氢盐处理证明,甲基化发生在转座元件 Nimbus 的多个拷贝中。

结论

这项研究首次详细描述了双脐螺中 DNA 甲基化,这是一种表观遗传信息的载体。我们在双脐螺基因组中观察到的 DNA 甲基化的一般特征与其他无脊椎动物物种的表观遗传研究报告的特征一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1ad/3681652/d763b67002c5/1756-3305-6-167-1.jpg

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