Molecular cell · 2020
Large DNA Methylation Nadirs Anchor Chromatin Loops Maintaining Hematopoietic Stem Cell Identity.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПоддержка правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Zhang Xiaotian, Jeong Mira, Huang Xingfan, Wang Xue Qing, Wang Xinyu, Zhou Wanding, Shamim Muhammad S, Gore Haley, Himadewi Pamela, Liu Yushuai, Bochkov Ivan D, Reyes Jaime, Doty Madison, Huang Yung-Hsin, Jung Haiyoung, Heikamp Emily, Aiden Aviva Presser, Li Wei, Su Jianzhong, Aiden Erez Lieberman, Goodell Margaret A
Аннотация
Higher-order chromatin structure and DNA methylation are implicated in multiple developmental processes, but their relationship to cell state is unknown. Here, we find that large (>7.3 kb) DNA methylation nadirs (termed "grand canyons") can form long loops connecting anchor loci that may be dozens of megabases (Mb) apart, as well as inter-chromosomal links. The interacting loci cover a total of ∼3.5 Mb of the human genome. The strongest interactions are associated with repressive marks made by the Polycomb complex and are diminished upon EZH2 inhibitor treatment. The data are suggestive of the formation of these loops by interactions between repressive elements in the loci, forming a genomic subcompartment, rather than by cohesion/CTCF-mediated extrusion. Interestingly, unlike previously characterized subcompartments, these interactions are present only in particular cell types, such as stem and progenitor cells. Our work reveals that H3K27me3-marked large DNA methylation grand canyons represent a set of very-long-range loops associated with cellular identity.
Предметные рубрики MeSH
CCCTC-Binding FactorCell DifferentiationChromatinDNA MethylationEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticGene Expression RegulationHematopoietic Stem CellsHistonesHomeodomain ProteinsHumansIn Situ Hybridization, FluorescenceLysineNuclear ProteinsSOXB1 Transcription FactorsShort Stature Homeobox ProteinTranscription Factors