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      Lineage-specific and single cell chromatin accessibility charts human hematopoiesis and leukemia evolution

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          Abstract

          We define the chromatin accessibility and transcriptional landscapes in thirteen human primary blood cell types that traverse 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 reveal the lineage ontogeny of genetic elements linked to diverse human diseases. In acute myeloid leukemia (AML), chromatin accessibility reveals unique regulatory evolution in cancer cells with progressive mutation burden. Single AML cells exhibit distinctive mixed regulome profiles of disparate developmental stages. A method to account for this regulatory heterogeneity identified cancer-specific deviations and implicated HOX factors as key regulators of pre-leukemic HSC characteristics. Thus, regulome dynamics can provide diverse insights into hematopoietic development and disease.

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          Most cited references35

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          Immunogenetics. Chromatin state dynamics during blood formation.

          Chromatin modifications are crucial for development, yet little is known about their dynamics during differentiation. Hematopoiesis provides a well-defined model to study chromatin state dynamics; however, technical limitations impede profiling of homogeneous differentiation intermediates. We developed a high-sensitivity indexing-first chromatin immunoprecipitation approach to profile the dynamics of four chromatin modifications across 16 stages of hematopoietic differentiation. We identify 48,415 enhancer regions and characterize their dynamics. We find that lineage commitment involves de novo establishment of 17,035 lineage-specific enhancers. These enhancer repertoire expansions foreshadow transcriptional programs in differentiated cells. Combining our enhancer catalog with gene expression profiles, we elucidate the transcription factor network controlling chromatin dynamics and lineage specification in hematopoiesis. Together, our results provide a comprehensive model of chromatin dynamics during development. Copyright © 2014, American Association for the Advancement of Science.
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            An expansive human regulatory lexicon encoded in transcription factor footprints

            Regulatory factor binding to genomic DNA protects the underlying sequence from cleavage by DNaseI, leaving nucleotide-resolution footprints. Using genomic DNaseI footprinting across 41 diverse cell and tissue types, we detected 45 million factor occupancy events within regulatory regions, representing differential binding to 8.4 million distinct short sequence elements. Here we show that this small genomic sequence compartment, roughly twice the size of the exome, encodes an expansive repertoire of conserved recognition sequences for DNA-binding proteins that nearly doubles the size of the human cis-regulatory lexicon. We find that genetic variants affecting allelic chromatin states are concentrated in footprints, and that these elements are preferentially sheltered from DNA methylation. High-resolution DNaseI cleavage patterns mirror nucleotide-level evolutionary conservation and track the crystallographic topography of protein-DNA interfaces, indicating that transcription factor structure has been evolutionarily imprinted on the human genome sequence. We identify a stereotyped 50 base-pair footprint that precisely defines the site of transcript origination within thousands of human promoters. Finally, we describe a large collection of novel regulatory factor recognition motifs that are highly conserved in both sequence and function, and exhibit cell-selective occupancy patterns that closely parallel major regulators of development, differentiation, and pluripotency.
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              Hematopoietic stem cell: self-renewal versus differentiation.

              The mammalian blood system, containing more than 10 distinct mature cell types, stands on one specific cell type, hematopoietic stem cell (HSC). Within the system, only HSCs possess the ability of both multipotency and self-renewal. Multipotency is the ability to differentiate into all functional blood cells. Self-renewal is the ability to give rise to HSC itself without differentiation. Since mature blood cells (MBCs) are predominantly short-lived, HSCs continuously provide more differentiated progenitors while properly maintaining the HSC pool size throughout life by precisely balancing self-renewal and differentiation. Thus, understanding the mechanisms of self-renewal and differentiation of HSC has been a central issue. In this review, we focus on the hierarchical structure of the hematopoietic system, the current understanding of microenvironment and molecular cues regulating self-renewal and differentiation of adult HSCs, and the currently emerging systems approaches to understand HSC biology. © 2010 John Wiley & Sons, Inc.
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                Author and article information

                Journal
                9216904
                2419
                Nat Genet
                Nat. Genet.
                Nature genetics
                1061-4036
                1546-1718
                26 July 2016
                15 August 2016
                October 2016
                15 February 2017
                : 48
                : 10
                : 1193-1203
                Affiliations
                [1 ]Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
                [2 ]Department of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA
                [3 ]Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA 94305, USA
                [4 ]Department of Genetics, Stanford University, Stanford, CA 94305, USA
                [5 ]Program in Biomedical Informatics, Stanford University School of Medicine, Stanford, CA 94305, USA
                [6 ]Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada
                [7 ]Department of Biology, Stanford University, Stanford, CA 94305, USA
                [8 ]Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA
                [9 ]Department of Computer Science, Stanford University, Stanford, CA 94305, USA
                Author notes
                Correspondence should be addressed to: R.M. ( rmajeti@ 123456stanford.edu ) or H.Y.C. ( howchang@ 123456stanford.edu )
                [10]

                These authors contributed equally to this work

                [11]

                These authors jointly directed this work

                Contact Information: Ravindra Majeti MD, PhD, Stanford University School of Medicine, Stanford Institute for Stem Cell Biology and Regenerative Medicine, Lokey Stem Cell Building, 265 Campus Drive, Stanford, CA 94305-5463, rmajeti@ 123456stanford.edu , Phone: 650-721-6376, Fax: 650-736-2961.

                Howard Y. Chang, MD, PhD, Stanford University School of Medicine, CCSR 2155c, 269 Campus Drive, Stanford, CA 94305-5168, howchang@ 123456stanford.edu , Phone: 650-736-0306, Fax: 650-723-8762

                Article
                NIHMS804249
                10.1038/ng.3646
                5042844
                27526324
                a87ba757-18cc-48a7-be46-7fb06a31f7cd

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