Bruggmann Rémy, Jagannathan Vidhya, Braunschweig Martin
Department of Biology, Bioinformatics, University of Bern, Berne, Switzerland.
PLoS One. 2013 Nov 4;8(11):e78691. doi: 10.1371/journal.pone.0078691. eCollection 2013.
In search of transmittable epigenetic marks we investigated gene expression in testes and sperm cells of differentially fed F0 boars from a three generation pig feeding experiment that showed phenotypic differences in the F2 generation. RNA samples from 8 testes of boars that received either a diet enriched in methylating micronutrients or a control diet were analyzed by microarray analysis. We found moderate differential expression between testes of differentially fed boars with a high FDR of 0.82 indicating that most of the differentially expressed genes were false positives. Nevertheless, we performed a pathway analysis and found disparate pathway maps of development_A2B receptor: action via G-protein alpha s, cell adhesion_Tight junctions and cell adhesion_Endothelial cell contacts by junctional mechanisms which show inconclusive relation to epigenetic inheritance. Four RNA samples from sperm cells of these differentially fed boars were analyzed by RNA-Seq methodology. We found no differential gene expression in sperm cells of the two groups (adjusted P-value>0.05). Nevertheless, we also explored gene expression in sperm by a pathway analysis showing that genes were enriched for the pathway maps of bacterial infections in cystic fibrosis (CF) airways, glycolysis and gluconeogenesis p.3 and cell cycle_Initiation of mitosis. Again, these pathway maps are miscellaneous without an obvious relationship to epigenetic inheritance. It is concluded that the methylating micronutrients moderately if at all affects RNA expression in testes of differentially fed boars. Furthermore, gene expression in sperm cells is not significantly affected by extensive supplementation of methylating micronutrients and thus RNA molecules could not be established as the epigenetic mark in this feeding experiment.
为了寻找可传递的表观遗传标记,我们在一项三代猪饲养实验中,研究了不同喂养方式的F0代公猪睾丸和精子细胞中的基因表达情况,该实验显示F2代存在表型差异。对8头接受富含甲基化微量营养素饮食或对照饮食的公猪的睾丸RNA样本进行了微阵列分析。我们发现,不同喂养方式的公猪睾丸之间存在中度差异表达,错误发现率(FDR)高达0.82,这表明大多数差异表达基因是假阳性。尽管如此,我们还是进行了通路分析,发现了发育_A2B受体:通过G蛋白αs起作用、细胞黏附_紧密连接以及细胞黏附_内皮细胞通过连接机制接触等不同的通路图谱,这些通路图谱与表观遗传遗传的关系尚无定论。对这些不同喂养方式的公猪精子细胞的4个RNA样本采用RNA测序方法进行了分析。我们发现两组精子细胞中没有差异基因表达(校正P值>0.05)。尽管如此,我们还通过通路分析探索了精子中的基因表达,结果显示,基因在囊性纤维化(CF)气道细菌感染、糖酵解和糖异生p.3以及细胞周期_有丝分裂起始等通路图谱中富集。同样,这些通路图谱杂乱无章,与表观遗传遗传没有明显关系。得出的结论是,甲基化微量营养素即使有影响,也只是适度影响不同喂养方式公猪睾丸中的RNA表达。此外,精子细胞中的基因表达不受甲基化微量营养素大量补充的显著影响,因此在该饲养实验中,RNA分子不能被确立为表观遗传标记。