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GEO help: Mouse over screen elements for information. |
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| Status |
Public on Sep 24, 2021 |
| Title |
Single-cell landscape of nuclear configuration and gene expression during stem cell differentiation and X inactivation |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing Other
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| Summary |
Mammalian development is associated with extensive changes in gene expression, chromatin accessibility, and nuclear structure. Here, we follow such changes associated with mouse embryonic stem cell differentiation and X inactivation by integrating, for the first time, allele-specific data obtained by high-throughput single-cell RNA-seq, ATAC-seq, and Hi-C. In differentiated cells, contact decay profiles, which clearly distinguish the active and inactive X chromosomes, reveal loss of the inactive X-specific structure at mitosis followed by a rapid reappearance, suggesting a bookkeeping mechanism. In differentiating embryonic stem cells, changes in contact decay profiles are detected in parallel on both the X chromosomes and autosomes, suggesting profound simultaneous reorganization. The onset of the inactive X-specific structure in single cells is notably delayed relative to that of gene silencing, consistent with the idea that chromatin compaction is a late event of X inactivation. Novel computational approaches to effectively align single-cell gene expression, chromatin accessibility, and 3D chromosome structure reveal that long-range structural changes to chromosomes appear as discrete events, unlike progressive changes in gene expression and chromatin accessibility.
### Competing Interest Statement
The authors have declared no competing interest.
### This SuperSeries is composed of the SubSeries listed below.
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| Overall design |
Refer to individual Series
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| Citation(s) |
34579774 |
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| Submission date |
Sep 21, 2021 |
| Last update date |
Oct 22, 2021 |
| Contact name |
4DN DCIC |
| E-mail(s) |
support@4dnucleome.org
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| Organization name |
4D Nucleome - Data Coordination and Integration Center
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| Street address |
10 Shattuck St
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| City |
Boston |
| State/province |
MA |
| ZIP/Postal code |
02115 |
| Country |
USA |
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| Platforms (2) |
| GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
| GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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| Samples (25)
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| GSM5593361 |
sci-ATAC-seq on F123-CASTx129 differentiated to embryoid body - 4DNEXUTXVJNS |
| GSM5593362 |
sci-ATAC-seq on F123-CASTx129 differentiated to embryoid body - 4DNEXOSQFCTM |
| GSM5593363 |
sci-ATAC-seq on F123-CASTx129 differentiated to embryoid body - 4DNEXXXQ7SNN |
| GSM5593364 |
sci-ATAC-seq on F123-CASTx129 - 4DNEXMJVA3ZW |
| GSM5593365 |
sci-ATAC-seq on F121-6-CASTx129 differentiated to neuronal stem cell - 4DNEXP788IVD |
| GSM5593366 |
sci-ATAC-seq on F121-6-CASTx129 differentiated to embryoid body - 4DNEXOLF62PK |
| GSM5593367 |
sci-ATAC-seq on F121-6-CASTx129 differentiated to embryoid body - 4DNEXOKNIX5B |
| GSM5593368 |
sci-ATAC-seq on F121-6-CASTx129 differentiated to embryoid body - 4DNEXX4XDGPO |
| GSM5593369 |
sci-ATAC-seq on F121-6-CASTx129 - 4DNEX55NM5L3 |
| GSM5593373 |
sci-RNA-seq on F123-CASTx129 differentiated to neuronal stem cell - 4DNEXAY3ALVE |
| GSM5593374 |
sci-RNA-seq on F123-CASTx129 differentiated to embryoid body - 4DNEX2VTS1YZ |
| GSM5593375 |
sci-RNA-seq on F123-CASTx129 differentiated to embryoid body - 4DNEXXCVEEE2 |
| GSM5593376 |
sci-RNA-seq on F123-CASTx129 differentiated to embryoid body - 4DNEXCWGVH6G |
| GSM5593377 |
sci-RNA-seq on F123-CASTx129 - 4DNEX7A9NPK2 |
| GSM5593378 |
sci-RNA-seq on F121-6-CASTx129 differentiated to neuronal stem cell - 4DNEXPGR1CVZ |
| GSM5593379 |
sci-RNA-seq on F121-6-CASTx129 differentiated to embryoid body - 4DNEXYO7LG9X |
| GSM5593380 |
sci-RNA-seq on F121-6-CASTx129 differentiated to embryoid body - 4DNEXT7D5EOI |
| GSM5593381 |
sci-RNA-seq on F121-6-CASTx129 differentiated to embryoid body - 4DNEXA8OVCDB |
| GSM5593382 |
sci-RNA-seq on F121-6-CASTx129 - 4DNEXNPCRAKI |
| GSM5620573 |
4DNEXLCFXRUP (F123_d20), 4DNEXOA4DNR8 (TsixStop_d20), 4DNEXTJOSWTW (F121_d20) |
| GSM5620574 |
4DNEX1BY7H2C (F123_d7), 4DNEXCDN76F9 (TsixStop_d7), 4DNEXJ33QCZU (TsixStop_d0), 4DNEXMYV77X1 (F121_d7) |
| GSM5620575 |
4DNEXK2CP3J1 (F121_d0), 4DNEXU9FJ24U (F123_d0) |
| GSM5620576 |
4DNEXMN3ZJ4X (d0), 4DNEXRMWXOKT (d3), 4DNEXVG7LXZE (d11), 4DNEXWHKWMSY (d7) |
| GSM5620577 |
4DNEXEE1N4JI, 4DNEXMNAHJPG, 4DNEXJNGKL32, 4DNEXXNEYDTM, 4DNEXPLD13JA, 4DNEXTLVDZQP |
| GSM5620578 |
4DNEXB7EWKCM (TsixStop_d0), 4DNEXJAHCEIN (TsixStop_d11), 4DNEXLZWN9VH (TsixStop_d7), 4DNEXV3C383J (TsixStop_d3) |
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| This SuperSeries is composed of the following SubSeries: |
| GSE184600 |
4DNESOUYRIO9 - sci-ATAC-seq on mESCs differentiated to embryoid body |
| GSE184602 |
4DNESCX7WHJ1 - sci-RNA-seq on mESCs differentiated to embryoid body |
| GSE185608 |
4DNESB7XYI9V - sci-Hi-C on mESCs differentiated to embryoid body |
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| Relations |
| BioProject |
PRJNA765363 |
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