A Genetically Encoded Probe for Live-Cell Imaging of H4K20 Monomethylation

被引:43
作者
Sato, Yuko [1 ]
Kujirai, Tomoya [2 ]
Arai, Ritsuko [3 ]
Asakawa, Haruhiko [4 ]
Ohtsuki, Chizuru [4 ]
Horikoshi, Naoki [2 ]
Yamagata, Kazuo [5 ]
Ueda, Jun [6 ]
Nagase, Takahiro [7 ]
Haraguchi, Tokuko [4 ,8 ]
Hiraoka, Yasushi [4 ,8 ]
Kimura, Akatsuki [3 ]
Kurumizaka, Hitoshi [2 ]
Kimura, Hiroshi [1 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Cell Biol Unit, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268501, Japan
[2] Waseda Univ, Grad Sch Adv Sci & Engn, Struct Biol Lab, Shinjuku Ku, Tokyo 1628480, Japan
[3] Natl Inst Genet, Struct Biol Ctr, Cell Architecture Lab, Mishima, Shizuoka 4118540, Japan
[4] Osaka Univ, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
[5] Kindai Univ, Fac Biol Oriented Sci & Technol, Wakayama 6496493, Japan
[6] Chubu Univ, Ctr Educ Lab Anim Res, Kasugai, Aichi 4878501, Japan
[7] Kazusa DNA Res Inst, Publ Relat Team, Chiba 2920818, Japan
[8] Natl Inst Informat & Commun Technol NICT, Adv ICT Res Inst, Kobe, Hyogo 6512492, Japan
基金
日本学术振兴会;
关键词
Histone modification; Inactive X chromosome; Intracellular antibody; Live-cell imaging; HISTONE H4; FISSION YEAST; BIOPHYSICAL PROPERTIES; DNA; METHYLATION; CHROMATIN; PR-SET7; METHYLTRANSFERASE; ACETYLATION; CHROMOSOMES;
D O I
10.1016/j.jmb.2016.08.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eukaryotic gene expression is regulated in the context of chromatin. Dynamic changes in post-translational histone modification are thought to play key roles in fundamental cellular functions such as regulation of the cell cycle, development, and differentiation. To elucidate the relationship between histone modifications and cellular functions, it is important to monitor the dynamics of modifications in single living cells. A genetically encoded probe called mintbody (modification-specific intracellular antibody), which is a single-chain variable fragment tagged with a fluorescent protein, has been proposed as a useful visualization tool. However, the efficacy of intracellular expression of antibody fragments has been limited, in part due to different environmental conditions in the cytoplasm compared to the endoplasmic reticulum where secreted proteins such as antibodies are folded. In this study, we have developed a new mintbody specific for histone H4 Lys20 monomethylation (H4K2Ome1). The specificity of the H4K2Ome1-mintbody in living cells was verified using yeast mutants and mammalian cells in which this target modification was diminished. Expression of the H4K20me1-mintbody allowed us to monitor the oscillation of H4K2Ome1 levels during the cell cycle. Moreover, dosage-compensated X chromosomes were visualized using the H4K20me1-mintbody in mouse and nematode cells. Using X-ray crystallography and mutational analyses, we identified critical amino acids that contributed to stabilization and/or proper folding of the mintbody. Taken together, these data provide important implications for future studies aimed at developing functional intracellular antibodies. Specifically, the H4K2Ome1-mintbody provides a powerful tool to track this particular histone modification in living cells and organisms. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:3885 / 3902
页数:18
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