Weyrich Alexandra, Schüllermann Tino, Heeger Felix, Jeschek Marie, Mazzoni Camila J, Chen Wei, Schumann Kathrin, Fickel Joerns
Leibniz-Institute for Zoo and Wildlife Research (IZW), Alfred-Kowalke-Str 17, D-10315 Berlin, Germany.
BMC Genomics. 2014 Nov 28;15(1):1036. doi: 10.1186/1471-2164-15-1036.
DNA methylation is a heritable mechanism that acts in response to environmental changes, lifestyle and diseases by influencing gene expression in eukaryotes. Epigenetic studies of wild organisms are mandatory to understand their role in e.g. adaptational processes in the great variety of ecological niches. However, strategies to address those questions on a methylome scale are widely missing. In this study we present such a strategy and describe a whole genome sequence and methylome analysis of the wild guinea pig.
We generated a full Wild guinea pig (Cavia aperea) genome sequence with enhanced coverage of methylated regions, benefiting from the available sequence of the domesticated relative Cavia porcellus. This new genome sequence was then used as reference to map the sequence reads of bisulfite treated Wild guinea pig sequencing libraries to investigate DNA-methylation patterns at nucleotide-specific level, by using our here described method, named 'DNA-enrichment-bisulfite-sequencing' (MEBS). The results achieved using MEBS matched those of standard methods in other mammalian model species. The technique is cost efficient, and incorporates both methylation enrichment results and a nucleotide-specific resolution even without a whole genome sequence available. Thus MEBS can be easily applied to extend methylation enrichment studies to a nucleotide-specific level.
The approach is suited to study methylomes of not yet sequenced mammals at single nucleotide resolution. The strategy is transferable to other mammalian species by applying the nuclear genome sequence of a close relative. It is therefore of interest for studies on a variety of wild species trying to answer evolutionary, adaptational, ecological or medical questions by epigenetic mechanisms.
DNA甲基化是一种可遗传的机制,通过影响真核生物中的基因表达来响应环境变化、生活方式和疾病。对野生生物进行表观遗传学研究对于理解它们在各种生态位的适应过程等方面的作用至关重要。然而,在甲基化组水平上解决这些问题的策略却普遍缺失。在本研究中,我们提出了这样一种策略,并描述了野生豚鼠的全基因组序列和甲基化组分析。
我们利用已有的家养豚鼠(豚鼠)的序列,生成了一个覆盖甲基化区域增强的完整野生豚鼠(豚鼠)基因组序列。然后,以这个新的基因组序列为参考,通过我们在此描述的名为“DNA富集亚硫酸氢盐测序”(MEBS)的方法,对经亚硫酸氢盐处理的野生豚鼠测序文库的序列读数进行映射,以在核苷酸特异性水平上研究DNA甲基化模式。使用MEBS获得的结果与其他哺乳动物模型物种的标准方法的结果相匹配。该技术具有成本效益,即使没有全基因组序列,也能整合甲基化富集结果和核苷酸特异性分辨率。因此,MEBS可以很容易地应用于将甲基化富集研究扩展到核苷酸特异性水平。
该方法适用于以单核苷酸分辨率研究尚未测序的哺乳动物的甲基化组。通过应用近亲的核基因组序列,该策略可转移到其他哺乳动物物种。因此,对于试图通过表观遗传机制回答进化、适应、生态或医学问题的各种野生物种的研究来说,它具有重要意义。