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Dynamic reorganization of nuclear architecture during human cardiogenesis [HiC-seq]

ABSTRACT: Dynamic reorganization of nuclear architecture during human cardiogenesis [HiC-seq]

PROVIDER: PRJNA417685 | ENA |

REPOSITORIES: ENA

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Dynamic reorganization of nuclear architecture during human cardiogenesis

Project description:Dynamic reorganization of nuclear architecture during human cardiogenesis

| PRJNA417681 | ENA

Dynamic reorganization of nuclear architecture during human cardiogenesis [HiC-seq]

Project description:While chromosomal architecture varies among cell types, little is known about how this organization is established or its role in development. We integrated Hi-C, RNA-seq and ATAC-seq during cardiac differentiation from human pluripotent stem cells to generate a comprehensive profile of chromosomal architecture. We identified active and repressive domains that are dynamic during cardiogenesis and recapitulate in vivo cardiomyocytes. During differentiation, heterochromatic regions condense in cis. In contrast, many cardiac-specific genes, such as TTN (titin), transition to an active compartment coincident with upregulation. Moreover, we identify a network of genes, including TTN, that share the heart-specific splicing factor, RBM20, and become associated in trans during differentiation, suggesting the existence of a 3D nuclear splicing factory. Our results demonstrate both the dynamic nature in nuclear architecture and provide insights into how developmental genes are coordinately regulated.

2018-01-04 | GSE106687 | GEO

Dynamic reorganization of nuclear architecture during human cardiogenesis [ATAC-seq]

Project description:Dynamic reorganization of nuclear architecture during human cardiogenesis [ATAC-seq]

| PRJNA417684 | ENA

Dynamic reorganization of nuclear architecture during human cardiogenesis [RNA-seq]

Project description:Dynamic reorganization of nuclear architecture during human cardiogenesis [RNA-seq]

| PRJNA417683 | ENA

Dynamic reorganization of nuclear architecture during human cardiogenesis [ATAC-seq]

2018-01-04 | GSE106689 | GEO

Dynamic reorganization of nuclear architecture during human cardiogenesis [RNA-seq]

2018-01-04 | GSE106688 | GEO

Reorganization of 3D chromatin architecture of rice genomes during heat stress (HiC)

Project description:Reorganization of 3D chromatin architecture of rice genomes during heat stress (HiC)

| PRJNA604027 | ENA

Dynamic reorganization of nuclear architecture during human cardiogenesis

Project description:This SuperSeries is composed of the SubSeries listed below.

2018-01-04 | GSE106690 | GEO

Chromatin architecture reorganization in somatic cell nuclear transfer embryos

Project description:Chromatin architecture reorganization in somatic cell nuclear transfer embryos

| PRJNA608976 | ENA

Chromatin architecture reorganization in somatic cell nuclear transfer embryos

Project description:The oocyte cytoplasm can reprogram somatic cell nucleus into a totipotent state but with low efficiency. The spatiotemporal chromatin organization of somatic cell nuclear transfer (SCNT) embryos remains elusive. Here, we examined higher-order chromatin structures of mouse SCNT embryos using an optimized low-input Hi-C approach. We found that the donor cell chromatin transformed to metaphase state rapidly after injection along with the dissolution of typical 3D chromatin structures. Intriguingly, the donor cell genome underwent a transition from mitotic metaphase-like state to meiosis metaphase II-like state within one hour after activation. Subsequently, weak chromatin compartments and topologically associating domains (TADs) emerged at 6 hours after activation. Then TADs were gradually removed until the 2-cell stage and then progressively reestablished. We found that relative few distal (> 2 Mb) interactions were present in 2-cell stage SCNT embryos. Also, obvious differences in compartment and TAD organization between fertilization-derived and SCNT embryos were observed in early stages (2-8 cell stages). Many interactions between super-enhancers and promoters were not successfully established in SCNT embryos, and these interactions were further shown important for zygotic genome activation (ZGA). Moreover, we demonstrate that the aberrant chromatin architecture reorganization in SCNT embryos may be due to the persistent H3K9me3 and can be partially rescued by the Kdm4d overexpression. This study therefore provides novel insight into chromatin architecture reorganization during SCNT embryo development.

2020-02-27 | GSE146001 | GEO

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