bioRxivGenomicsPreprint
Stepwise reorganization of chromosome conformation and nuclear organization during stem cell differentiation
Xiangru HuoiD, Denis L. Lafontaine, Thomas M. ReimonniD, Liyan YangiD, Richard SilleriD, Jack D. HueyiD, Jiang Min, Aleksandra A. GalitsynaiD, Vedat Yilma, Krishna Mohan ParsiiD, Emily NavarreteiD, Hoang TraniD, Leonid A. MirnyiD, René MaehriD, Johan Harmen GibcusiD, Job DekkeriD, Nezar A. AbdennuriD
Abstract
Nuclear organization is a fundamental feature of cell identity and cell fate determination. Compared with differentiated cells, pluripotent stem cells exhibit markedly distinct nuclear architecture at multiple levels, including chromosome folding, lamina association, histone modification landscapes and nuclear body organization. Although individual aspects of this reorganization have been characterized, how and in what order these features are remodeled as cells commit to a lineage remains poorly understood. Here, we temporally map nuclear reorganization across five stages of an in vitro differentiation system of human embryonic stem cells through definitive endoderm and hepatoblast intermediates into hepatocyte-like cells. By integrating Hi-C, RNA-seq, ATAC-seq, ChIP-seq, and CUT&RUN data, we establish a genome-wide framework linking structural, epigenetic, and transcriptional changes across differentiation. Combined with immunofluorescence imaging, chromosome painting, and liquid chromatin Hi-C (LC-Hi-C) we show that nuclear reorganization proceeds in a stepwise and temporally ordered manner through three major transitions. In the first transition, chromosomes condense into defined territories concurrent with transient anchoring of centromere-proximal regions to the nuclear periphery. In a second transition, active and inactive chromatin segregate, leading to stronger compartmentalization. This coincides with deposition and peripheralization of H3K9me2-marked chromatin and morphological changes in nuclear speckles, while chromatin conformation at speckle-associated regions stabilizes. In a third transition, after lineage-specific genes are activated, chromatin interactions globally stabilize, establishing a more stable nuclear architecture on top of these earlier large-scale structural rearrangements. Together, our results define a stepwise framework for nuclear reorganization during human embryonic stem cell differentiation and reveal that the transition from pluripotency to a differentiated state proceeds through coordinated, temporally ordered structural events.
- organism: human
- assay: Hi-C
- assay: bulk RNA-seq
- assay: ATAC-seq
- assay: ChIP-seq
- research focus: trajectory inference
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- approach: experimental assay
- Citations
- 0
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