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DNA Methylation Dynamics of Human Hematopoietic Stem Cell Differentiation

机译:人造血干细胞分化的DNA甲基化动力学

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Hematopoietic stem cells give rise to all blood cells in a differentiation process that involves widespread epigenome remodeling. Here we present genome-wide reference maps of the associated DNA methylation dynamics. We used a meta-epigenomic approach that combines DNA methylation profiles across many small pools of cells and performed single-cell methylome sequencing to assess cell-to-cell heterogeneity. The resulting dataset identified characteristic differences between HSCs derived from fetal liver, cord blood, bone marrow, and peripheral blood. We also observed lineage-specific DNA methylation between myeloid and lymphoid progenitors, characterized immature multi-lymphoid progenitors, and detected progressive DNA methylation differences in maturing megakaryocytes. We linked these patterns to gene expression, histone modifications, and chromatin accessibility, and we used machine learning to derive a model of human hematopoietic differentiation directly from DNA methylation data. Our results contribute to a better understanding of human hematopoietic stem cell differentiation and provide a framework for studying blood-linked diseases.
机译:造血干细胞在涉及广泛的表观基因组重塑的分化过程中产生所有血细胞。在这里,我们介绍了相关的DNA甲基化动力学的全基因组参考图。我们使用了一种元表观基因组学方法,该方法结合了许多小细胞池中的DNA甲基化谱,并进行了单细胞甲基化测序,以评估细胞间异质性。结果数据集确定了源自胎儿肝脏,脐带血,骨髓和外周血的HSC之间的特征差异。我们还观察到髓样和淋巴样祖细胞之间的谱系特异性DNA甲基化,表征未成熟的多淋巴样祖细胞,并检测到成熟的巨核细胞中进行性DNA甲基化的差异。我们将这些模式与基因表达,组蛋白修饰和染色质可及性联系起来,并且我们使用机器学习直接从DNA甲基化数据中得出了人类造血分化的模型。我们的结果有助于更好地了解人类造血干细胞的分化,并为研究血液相关疾病提供了框架。

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