| Literature DB >> 27851973 |
Mark A Le Gros1, E Josephine Clowney2, Angeliki Magklara3, Angela Yen4, Eirene Markenscoff-Papadimitriou5, Bradley Colquitt5, Markko Myllys6, Manolis Kellis4, Stavros Lomvardas7, Carolyn A Larabell8.
Abstract
The realization that nuclear distribution of DNA, RNA, and proteins differs between cell types and developmental stages suggests that nuclear organization serves regulatory functions. Understanding the logic of nuclear architecture and how it contributes to differentiation and cell fate commitment remains challenging. Here, we use soft X-ray tomography (SXT) to image chromatin organization, distribution, and biophysical properties during neurogenesis in vivo. Our analyses reveal that chromatin with similar biophysical properties forms an elaborate connected network throughout the entire nucleus. Although this interconnectivity is present in every developmental stage, differentiation proceeds with concomitant increase in chromatin compaction and re-distribution of condensed chromatin toward the nuclear core. HP1β, but not nucleosome spacing or phasing, regulates chromatin rearrangements because it governs both the compaction of chromatin and its interactions with the nuclear envelope. Our experiments introduce SXT as a powerful imaging technology for nuclear architecture.Entities:
Keywords: chromatin; differentiation; neurogenesis; nuclear organization; nucleus; olfactory sensory neurons; soft X-ray tomography
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Year: 2016 PMID: 27851973 PMCID: PMC5135017 DOI: 10.1016/j.celrep.2016.10.060
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423