Siu Celia, Wiseman Sam, Gakkhar Sitanshu, Heravi-Moussavi Alireza, Bilenky Misha, Carles Annaick, Sierocinski Thomas, Tam Angela, Zhao Eric, Kasaian Katayoon, Moore Richard A, Mungall Andrew J, Walker Blair, Thomson Thomas, Marra Marco A, Hirst Martin, Jones Steven J M
Canada's Michael Smith Genome Sciences CentreBC Cancer Agency, Vancouver, Canada.
Department of SciencesUniversity of British Columbia, Vancouver, Canada.
J Endocrinol. 2017 Nov;235(2):153-165. doi: 10.1530/JOE-17-0145. Epub 2017 Aug 14.
The thyroid gland, necessary for normal human growth and development, functions as an essential regulator of metabolism by the production and secretion of appropriate levels of thyroid hormone. However, assessment of abnormal thyroid function may be challenging suggesting a more fundamental understanding of normal function is needed. One way to characterize normal gland function is to study the epigenome and resulting transcriptome within its constituent cells. This study generates the first published reference epigenomes for human thyroid from four individuals using ChIP-seq and RNA-seq. We profiled six histone modifications (H3K4me1, H3K4me3, H3K27ac, H3K36me3, H3K9me3, H3K27me3), identified chromatin states using a hidden Markov model, produced a novel quantitative metric for model selection and established epigenomic maps of 19 chromatin states. We found that epigenetic features characterizing promoters and transcription elongation tend to be more consistent than regions characterizing enhancers or Polycomb-repressed regions and that epigenetically active genes consistent across all epigenomes tend to have higher expression than those not marked as epigenetically active in all epigenomes. We also identified a set of 18 genes epigenetically active and consistently expressed in the thyroid that are likely highly relevant to thyroid function. Altogether, these epigenomes represent a powerful resource to develop a deeper understanding of the underlying molecular biology of thyroid function and provide contextual information of thyroid and human epigenomic data for comparison and integration into future studies.
甲状腺对于人类的正常生长和发育至关重要,它通过产生和分泌适量的甲状腺激素,发挥着新陈代谢的重要调节作用。然而,评估甲状腺功能异常可能具有挑战性,这表明需要对正常功能有更深入的了解。表征正常甲状腺功能的一种方法是研究其组成细胞内的表观基因组和由此产生的转录组。本研究利用ChIP-seq和RNA-seq技术,首次公布了来自四名个体的人类甲状腺参考表观基因组。我们分析了六种组蛋白修饰(H3K4me1、H3K4me3、H3K27ac、H3K36me3、H3K9me3、H3K27me3),使用隐马尔可夫模型识别染色质状态,生成了一种用于模型选择的新型定量指标,并建立了19种染色质状态的表观基因组图谱。我们发现,表征启动子和转录延伸的表观遗传特征往往比表征增强子或多梳抑制区域的特征更一致,并且在所有表观基因组中表观遗传活跃的基因往往比在所有表观基因组中未被标记为表观遗传活跃的基因具有更高的表达。我们还鉴定出一组在甲状腺中表观遗传活跃且持续表达的18个基因,它们可能与甲状腺功能高度相关。总之,这些表观基因组是一种强大的资源,有助于更深入地了解甲状腺功能的潜在分子生物学,并为甲状腺和人类表观基因组数据提供背景信息,以便进行比较并整合到未来的研究中。