| Literature DB >> 27890612 |
Masako Koyama1, Wataru Nagakura1, Hiroki Tanaka1, Tomoya Kujirai1, Yuji Chikashige2, Tokuko Haraguchi3, Yasushi Hiraoka3, Hitoshi Kurumizaka4.
Abstract
Schizosaccharomyces pombe, which has a small genome but shares many physiological functions with higher eukaryotes, is a useful single-cell, model eukaryotic organism. In particular, many features concerning chromatin structure and dynamics, including heterochromatin, centromeres, telomeres, and DNA replication origins, are well conserved between S. pombe and higher eukaryotes. However, the S. pombe nucleosome, the fundamental structural unit of chromatin, has not been reconstituted in vitro. In the present study, we established the method to purify S. pombe histones H2A, H2B, H3, and H4, and successfully reconstituted the S. pombe nucleosome in vitro. Our thermal stability assay and micrococcal nuclease treatment assay revealed that the S. pombe nucleosome is markedly unstable and its DNA ends are quite accessible, as compared to the canonical human nucleosome. These findings are important to understand the mechanisms of epigenetic genomic DNA regulation in fission yeast.Entities:
Keywords: Histones; Micrococcal nuclease; Nucleosome; Reconstitution; Schizosaccharomyces pombe; Thermal stability
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Year: 2016 PMID: 27890612 DOI: 10.1016/j.bbrc.2016.11.130
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575