Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo

Stem cell differentiation requires dramatic changes in gene expression and global remodeling of chromatin architecture. How and when chromatin remodels relative to the transcriptional, behavioral, and morphological changes during differentiation remain unclear, particularly in an intact tissue conte...

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Bibliographic Details
Published in:eLife Vol. 12
Main Authors: May, Dennis, Yun, Sangwon, Gonzalez, David G, Park, Sangbum, Chen, Yanbo, Lathrop, Elizabeth, Cai, Biao, Xin, Tianchi, Zhao, Hongyu, Wang, Siyuan, Gonzalez, Lauren E, Cockburn, Katie, Greco, Valentina
Format: Journal Article
Language:English
Published: England eLife Sciences Publications, Ltd 07-03-2023
eLife Sciences Publications Ltd
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Summary:Stem cell differentiation requires dramatic changes in gene expression and global remodeling of chromatin architecture. How and when chromatin remodels relative to the transcriptional, behavioral, and morphological changes during differentiation remain unclear, particularly in an intact tissue context. Here, we develop a quantitative pipeline which leverages fluorescently-tagged histones and longitudinal imaging to track large-scale chromatin compaction changes within individual cells in a live mouse. Applying this pipeline to epidermal stem cells, we reveal that cell-to-cell chromatin compaction heterogeneity within the stem cell compartment emerges independent of cell cycle status, and instead is reflective of differentiation status. Chromatin compaction state gradually transitions over days as differentiating cells exit the stem cell compartment. Moreover, establishing live imaging of ( ) nascent RNA, which marks the onset of stem cell differentiation, we find that transcription is highly dynamic and largely precedes the global chromatin compaction changes associated with differentiation. Together, these analyses reveal that stem cell differentiation involves dynamic transcriptional states and gradual chromatin rearrangement.
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These authors contributed equally to this work.
ISSN:2050-084X
2050-084X
DOI:10.7554/elife.83444