Domaschenz Renae, Livernois Alexandra M, Rao Sudha, Ezaz Tariq, Deakin Janine E
Institute for Applied Ecology, University of Canberra, Canberra, ACT 2601 Australia.
Present address: John Curtin School of Medical Research, The Australian National University, Canberra, ACT Australia.
Mol Cytogenet. 2015 Dec 30;8:104. doi: 10.1186/s13039-015-0208-6. eCollection 2015.
Studies of model organisms have demonstrated that DNA cytosine methylation and histone modifications are key regulators of gene expression in biological processes. Comparatively little is known about the presence and distribution of epigenetic marks in non-model amniotes such as non-avian reptiles whose genomes are typically packaged into chromosomes of distinct size classes. Studies of chicken karyotypes have associated the gene-richness and high GC content of microchromosomes with a distinct epigenetic landscape. To determine whether this is likely to be a common feature of amniote microchromosomes, we have analysed the distribution of epigenetic marks using immunofluorescence on metaphase chromosomes of the central bearded dragon (Pogona vitticeps). This study is the first to study the distribution of epigenetic marks on non-avian reptile chromosomes.
We observed an enrichment of DNA cytosine methylation, active modifications H3K4me2 and H3K4me3, as well as the repressive mark H3K27me3 in telomeric regions on macro and microchromosomes. Microchromosomes were hypermethylated compared to macrochromosomes, as they are in chicken. However, differences between macro- and microchromosomes for histone modifications associated with actively transcribed or repressed DNA were either less distinct or not detectable.
Hypermethylation of microchromosomes compared to macrochromosomes is a shared feature between P. vitticeps and avian species. The lack of the clear distinction between macro- and microchromosome staining patterns for active and repressive histone modifications makes it difficult to determine at this stage whether microchrosome hypermethylation is correlated with greater gene density as it is in aves, or associated with the greater GC content of P. vitticeps microchromosomes compared to macrochromosomes.
对模式生物的研究表明,DNA胞嘧啶甲基化和组蛋白修饰是生物过程中基因表达的关键调节因子。对于非模式羊膜动物(如非鸟类爬行动物)中表观遗传标记的存在和分布,人们了解得相对较少,这些动物的基因组通常被包装成不同大小类别的染色体。对鸡核型的研究将微染色体的基因丰富性和高GC含量与独特的表观遗传景观联系起来。为了确定这是否可能是羊膜动物微染色体的一个共同特征,我们使用免疫荧光技术分析了中部鬃狮蜥(Pogona vitticeps)中期染色体上表观遗传标记的分布。这项研究是首次对非鸟类爬行动物染色体上表观遗传标记的分布进行研究。
我们观察到在大染色体和微染色体的端粒区域,DNA胞嘧啶甲基化、活性修饰H3K4me2和H3K4me3以及抑制标记H3K27me3都有富集。与大染色体相比,微染色体高度甲基化,就像在鸡中一样。然而,与活跃转录或抑制的DNA相关的组蛋白修饰在大染色体和微染色体之间的差异要么不太明显,要么无法检测到。
与大染色体相比,微染色体的高度甲基化是鬃狮蜥和鸟类共有的特征。在活跃和抑制的组蛋白修饰方面,大染色体和微染色体的染色模式缺乏明显差异,这使得在现阶段难以确定微染色体的高度甲基化是否像在鸟类中那样与更高的基因密度相关,或者与鬃狮蜥微染色体相比大染色体更高的GC含量有关。