Density imaging of heterochromatin in live cells using orientation-independent-DIC microscopy
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In eukaryotic cells, highly condensed inactive/silenced chromatin has long been called “heterochromatin.” However, recent research suggests that such regions are in fact not fully transcriptionally silent and that there exists only a moderate access barrier to heterochromatin. To further investigate this issue, it is critical to elucidate the physical properties of heterochromatin such as its total density in live cells. Here, using orientation-independent differential interference contrast (OI-DIC) microscopy, which is capable of mapping optical path differences, we investigated the density of the total materials in pericentric foci, a representative heterochromatin model, in live mouse NIH3T3 cells. We demonstrated that the total density of heterochromatin (208 mg/ml) was only 1.53-fold higher than that of the surrounding euchromatic regions (136 mg/ml) while the DNA density of heterochromatin was 5.5- to 7.5-fold higher. We observed similar minor differences in density in typical facultative heterochromatin, the inactive human X chromosomes. This surprisingly small difference may be due to that nonnucleosomal materials (proteins/RNAs) (∼120 mg/ml) are dominant in both chromatin regions. Monte Carlo simulation suggested that nonnucleosomal materials contribute to creating a moderate access barrier to heterochromatin, allowing minimal protein access to functional regions. Our OI-DIC imaging offers new insight into the live cellular environments.
© The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Molecular Biology of the Cell 28 (2017): 3349-3359, doi:10.1091/mbc.E17-06-0359.
Suggested CitationArticle: Imai, Ryosuke, Nozaki, Tadasu, Tani, Tomomi, Kaizu, Kazunari, Hibino, Kayo, Ide, Satoru, Tamura, Sachiko, Takahashi, Koichi, Shribak, Michael, Maeshima, Kazuhiro, "Density imaging of heterochromatin in live cells using orientation-independent-DIC microscopy", Molecular Biology of the Cell 28 (2017): 3349-3359, DOI:10.1091/mbc.E17-06-0359, https://hdl.handle.net/1912/9474
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