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The landscape of accessible chromatin in mammalian preimplantation embryos

机译:哺乳动物植入前胚胎中可及染色质的景观

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摘要

In mammals, extensive chromatin reorganization is essential for reprogramming terminally committed gametes to a totipotent state during preimplantation development. However, the global chromatin landscape and its dynamics in this period remain unexplored. Here we report a genome-wide map of accessible chromatin in mouse preimplantation embryos using an improved assay for transposase-accessible chromatin with high throughput sequencing (ATAC-seq) approach with CRISPR/Cas9-assisted mitochondrial DNA depletion. We show that despite extensive parental asymmetry in DNA methylomes, the chromatin accessibility between the parental genomes is globally comparable after major zygotic genome activation (ZGA). Accessible chromatin in early embryos is widely shaped by transposable elements and overlaps extensively with putative cis-regulatory sequences. Unexpectedly, accessible chromatin is also found near the transcription end sites of active genes. By integrating the maps of cis-regulatory elements and single-cell transcriptomes, we construct the regulatory network of early development, which helps to identify the key modulators for lineage specification. Finally, we find that the activities of cis-regulatory elements and their associated open chromatin diminished before major ZGA. Surprisingly, we observed many loci showing non-canonical, large open chromatin domains over the entire transcribed units in minor ZGA, supporting the presence of an unusually permissive chromatin state. Together, these data reveal a unique spatiotemporal chromatin configuration that accompanies early mammalian development.
机译:在哺乳动物中,广泛的染色质重组对于在植入前发育过程中将最终定殖的配子重新编程为全能状态至关重要。然而,这一时期的全球染色质格局及其动态仍未得到探索。在这里,我们报告了使用转染酶可访问的染色质的改进测定方法,利用CRISPR / Cas9辅助线粒体DNA耗竭的高通量测序(ATAC-seq)方法,对小鼠植入前胚胎中可访问的染色质进行了全基因组图谱分析。我们显示,尽管在DNA甲基化组中存在广泛的亲本不对称性,但在主要合子基因组激活(ZGA)后,亲本基因组之间的染色质可及性在全球具有可比性。早期胚胎中可及的染色质被转座因子广泛地塑造,并与推定的顺式调控序列广泛重叠。出乎意料的是,在活性基因的转录末端附近也发现了可及的染色质。通过整合顺式调控元件和单细胞转录组的图谱,我们构建了早期开发的调控网络,这有助于确定谱系规格的关键调控因子。最后,我们发现在主要ZGA之前,顺式调控元件及其相关的开放染色质的活性降低了。出乎意料的是,我们观察到许多基因座在较小的ZGA的整个转录单位中显示出非规范的,大的开放染色质结构域,支持存在异常允许的染色质状态。总之,这些数据揭示了伴随早期哺乳动物发育的独特的时空染色质构型。

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  • 来源
    《Nature》 |2016年第7609期|652-657|共6页
  • 作者单位

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China|Tsinghua Univ, Sch Life Sci, Joint Grad Program Peking Tsinghua NIBS, Beijing 100084, Peoples R China;

    Peking Univ, Acad Adv Interdisciplinary Studies, PKU THU Ctr Life Sci, Beijing 100871, Peoples R China;

    Peking Univ, Coll Life Sci, Joint Grad Program Peking Tsinghua NIBS, Beijing 100871, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Life Sci, Joint Grad Program Peking Tsinghua NIBS, Beijing 100084, Peoples R China|Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Synthet & Syst Biol, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Med, Ctr Stem Cell Biol & Regenerat Med, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    ASTAR, Singapore Inst Clin Sci, Singapore 117609, Singapore;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Med, Ctr Stem Cell Biol & Regenerat Med, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Med, Beijing 100084, Peoples R China;

    ASTAR, Singapore Inst Clin Sci, Singapore 117609, Singapore|ASTAR, Inst Mol & Cell Biol, Singapore 138673, Singapore;

    Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Med, Ctr Stem Cell Biol & Regenerat Med, Beijing 100084, Peoples R China;

    Tsinghua Univ, Sch Life Sci, Joint Grad Program Peking Tsinghua NIBS, Beijing 100084, Peoples R China|Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Synthet & Syst Biol, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China;

    Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Stem Cell Biol & Regenerat Med, THU PKU Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China|Tsinghua Univ, Sch Life Sci, Joint Grad Program Peking Tsinghua NIBS, Beijing 100084, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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