生物
染色质
造血
干细胞
谱系(遗传)
遗传学
造血干细胞
计算生物学
增强子
白血病
表观遗传学
髓样
基因
癌症研究
转录因子
DNA甲基化
基因表达
作者
M. Ryan Corces,Jason D. Buenrostro,Beijing Wu,Peyton Greenside,Steven M. Chan,Julie L. Koenig,M Snyder,Jonathan K. Pritchard,Anshul Kundaje,William J. Greenleaf,Ravindra Majeti,Howard Y. Chang
出处
期刊:Nature Genetics
[Springer Nature]
日期:2016-08-15
卷期号:48 (10): 1193-1203
被引量:1135
摘要
We define the chromatin accessibility and transcriptional landscapes in 13 human primary blood cell types that span the hematopoietic hierarchy. Exploiting the finding that the enhancer landscape better reflects cell identity than mRNA levels, we enable 'enhancer cytometry' for enumeration of pure cell types from complex populations. We identify regulators governing hematopoietic differentiation and further show the lineage ontogeny of genetic elements linked to diverse human diseases. In acute myeloid leukemia (AML), chromatin accessibility uncovers unique regulatory evolution in cancer cells with a progressively increasing mutation burden. Single AML cells exhibit distinctive mixed regulome profiles corresponding to disparate developmental stages. A method to account for this regulatory heterogeneity identified cancer-specific deviations and implicated HOX factors as key regulators of preleukemic hematopoietic stem cell characteristics. Thus, regulome dynamics can provide diverse insights into hematopoietic development and disease.
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