Strepetkaitė Dovilė, Alzbutas Gediminas, Astromskas Eimantas, Lagunavičius Arūnas, Sabaliauskaitė Rasa, Arbačiauskas Kęstutis, Lazutka Juozas
Department of Botany and Genetics, Vilnius University, 21 Čiurlionis Str., LT-03101 Vilnius, Lithuania.
Thermo Fisher Scientific Baltics, Graičiūno g. 8, LT-02241 Vilnius, Lithuania.
Genes (Basel). 2015 Dec 31;7(1):1. doi: 10.3390/genes7010001.
The aim of our study was to analyze the presence of 5-methyl-cytosine (5-mC) and 5-hydroxymethyl-cytosine (5-hmC) in the genome of crustacean Daphnia pulex. First, the presence of 5-mC and 5-hmC in genomic DNA was demonstrated by using antibodies specific to either 5-mC or 5-hmC. Then, analysis of 5-mC and 5-hmC using pairs of restriction enzymes with different sensitivity to methylation and hydroxymethylation confirmed the presence of both modifications in selected regions of three genes (Cox4, Cand2 and Ephx1). To get a detailed picture of 5-hmC distribution over the D. pulex genome, we performed 5-hmC enrichment and sequenced the enriched fraction using next generation sequencing and non-enriched library (input) as a control. Comparison of input and enriched libraries showed that 5-hmC in exons is twice as frequent as in introns. Functional analysis indicated that 5-hmC abundance is associated with genes that are involved in the adenylate cyclase-activating G-protein-coupled receptor signaling pathway, molting cycles, morphogenesis and cell fate determination. Genes that lack 5-hmC tend to be involved in the regulation of the transforming growth factor beta receptor signaling pathway and in many mRNA-related processes. Our results suggest that epigenetic modifications are present in the genome of D. pulex and most likely are involved in the regulation of gene expression of this crustacean.
我们研究的目的是分析甲壳纲动物大型溞基因组中5-甲基胞嘧啶(5-mC)和5-羟甲基胞嘧啶(5-hmC)的存在情况。首先,通过使用针对5-mC或5-hmC的特异性抗体来证明基因组DNA中5-mC和5-hmC的存在。然后,使用对甲基化和羟甲基化具有不同敏感性的限制性酶对来分析5-mC和5-hmC,证实了在三个基因(Cox4、Cand2和Ephx1)的选定区域中存在这两种修饰。为了详细了解大型溞基因组中5-hmC的分布情况,我们进行了5-hmC富集,并使用下一代测序技术对富集部分进行测序,同时将未富集文库(输入)作为对照。输入文库和富集文库的比较表明,外显子中的5-hmC频率是内含子中的两倍。功能分析表明,5-hmC的丰度与参与腺苷酸环化酶激活的G蛋白偶联受体信号通路、蜕皮周期、形态发生和细胞命运决定的基因相关。缺乏5-hmC的基因往往参与转化生长因子β受体信号通路的调节以及许多与mRNA相关的过程。我们的结果表明,表观遗传修饰存在于大型溞的基因组中,并且很可能参与了这种甲壳纲动物基因表达的调控。