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West Ashley Library
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Folly Beach Library
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Phone: (843) 588-2001
Edgar Allan Poe/Sullivan's Island Library
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Wando Mount Pleasant Library
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9 a.m. – 6 p.m.
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Evidence for low nanocompaction of heterochromatin in living embryonic stem cells.
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- Author(s): Dupont, Claire; Chahar, Dhanvantri; Trullo, Antonio; Gostan, Thierry; Surcis, Caroline; Grimaud, Charlotte; Fisher, Daniel; Feil, Robert; Llères, David
- Source:
EMBO Journal; Jun2023, Vol. 42 Issue 12, p1-22, 22p- Subject Terms:
- Source:
- Additional Information
- Abstract: Despite advances in the identification of chromatin regulators and genome interactions, the principles of higher‐order chromatin structure have remained elusive. Here, we applied FLIM‐FRET microscopy to analyse, in living cells, the spatial organisation of nanometre range proximity between nucleosomes, which we called "nanocompaction." Both in naive embryonic stem cells (ESCs) and in ESC‐derived epiblast‐like cells (EpiLCs), we find that, contrary to expectations, constitutive heterochromatin is much less compacted than bulk chromatin. The opposite was observed in fixed cells. HP1α knockdown increased nanocompaction in living ESCs, but this was overridden by loss of HP1β, indicating the existence of a dynamic HP1‐dependent low compaction state in pluripotent cells. Depletion of H4K20me2/3 abrogated nanocompaction, while increased H4K20me3 levels accompanied the nuclear reorganisation during EpiLCs induction. Finally, the knockout of the nuclear cellular‐proliferation marker Ki‐67 strongly reduced both interphase and mitotic heterochromatin nanocompaction in ESCs. Our data indicate that, contrary to prevailing models, heterochromatin is not highly compacted at the nanoscale but resides in a dynamic low nanocompaction state that depends on H4K20me2/3, the balance between HP1 isoforms, and Ki‐67. Synopsis: Quantitative FLIM‐FRET imaging of nanometre‐scale distances between nucleosomes spatially maps "nanocompaction" in living mouse pluripotent cells. Heterochromatin has low nanocompaction levels that depend on the balance between HP1 isoforms, Ki‐67 and H4K20me2/3. FLIM‐FRET microscopy assays close proximity between nucleosomes : "nanocompaction".Heterochromatin shows low nanocompaction in living pluripotent stem cells.HP1α knockdown increases heterochromatin nanocompaction in living stem cells.HP1β, H4K20me2/3 and Ki‐67 protein maintain close proximity between nucleosomes within heterochromatin.Cell fixation artificially increases nanocompaction levels. [ABSTRACT FROM AUTHOR]
- Abstract: Copyright of EMBO Journal is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Abstract:
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