Blizard Institute, Barts and The London School of Medicine and Dentistry, QMUL, London E1 2AT, UK.
Université Côte d'Azur, Inserm, CNRS, IRCAN, Nice, France.
Nucleic Acids Res. 2022 Apr 8;50(6):e33. doi: 10.1093/nar/gkab1232.
Despite a vast expansion in the availability of epigenomic data, our knowledge of the chromatin landscape at interspersed repeats remains highly limited by difficulties in mapping short-read sequencing data to these regions. In particular, little is known about the locus-specific regulation of evolutionarily young transposable elements (TEs), which have been implicated in genome stability, gene regulation and innate immunity in a variety of developmental and disease contexts. Here we propose an approach for generating locus-specific protein-DNA binding profiles at interspersed repeats, which leverages information on the spatial proximity between repetitive and non-repetitive genomic regions. We demonstrate that the combination of HiChIP and a newly developed mapping tool (PAtChER) yields accurate protein enrichment profiles at individual repetitive loci. Using this approach, we reveal previously unappreciated variation in the epigenetic profiles of young TE loci in mouse and human cells. Insights gained using our method will be invaluable for dissecting the molecular determinants of TE regulation and their impact on the genome.
尽管表观基因组数据的可用性有了巨大的扩展,但由于将短读测序数据映射到这些区域的困难,我们对散布重复序列的染色质景观的了解仍然非常有限。特别是,关于进化年轻的转座元件(TEs)的位置特异性调控知之甚少,这些元件在多种发育和疾病情况下与基因组稳定性、基因调控和先天免疫有关。在这里,我们提出了一种在散布重复序列中生成位置特异性蛋白-DNA 结合图谱的方法,该方法利用了重复和非重复基因组区域之间空间接近性的信息。我们证明,HiChIP 与新开发的映射工具(PAtChER)的结合可以在单个重复基因座上产生准确的蛋白富集图谱。使用这种方法,我们揭示了在小鼠和人类细胞中年轻 TE 基因座的表观基因组图谱以前未被认识到的差异。我们方法获得的见解对于剖析 TE 调控的分子决定因素及其对基因组的影响将是非常宝贵的。