論文

査読有り
2018年2月5日

A Transient Rise in Free Mg2+ Ions Released from ATP-Mg Hydrolysis Contributes to Mitotic Chromosome Condensation

Current Biology
  • Kazuhiro Maeshima
  • Tomoki Matsuda
  • Yutaka Shindo
  • Hiromi Imamura
  • Sachiko Tamura
  • Ryosuke Imai
  • Syoji Kawakami
  • Ryosuke Nagashima
  • Tomoyoshi Soga
  • Hiroyuki Noji
  • Kotaro Oka
  • Takeharu Nagai
  • 全て表示

28
3
開始ページ
444
終了ページ
451.e6
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.cub.2017.12.035
出版者・発行元
Cell Press

For cell division, negatively charged chromatin, in which nucleosome fibers (10 nm fibers) are irregularly folded [1–5], must be condensed into chromosomes and segregated. While condensin and other proteins are critical for organizing chromatin into the appropriate chromosome shape [6–17], free divalent cations such as Mg2+ and Ca2+, which condense chromatin or chromosomes in vitro [18–28], have long been considered important, especially for local condensation, because the nucleosome fiber has a net negative charge and is by itself stretched like “beads on a string” by electrostatic repulsion. For further folding, other positively charged factors are required to decrease the charge and repulsion [29]. However, technical limitations to measure intracellular free divalent cations, but not total cations [30], especially Mg2+, have prevented us from elucidating their function. Here, we developed a Förster resonance energy transfer (FRET)-based Mg2+ indicator that monitors free Mg2+ dynamics throughout the cell cycle. By combining this indicator with Ca2+ [31] and adenosine triphosphate (ATP) [32] indicators, we demonstrate that the levels of free Mg2+, but not Ca2+, increase during mitosis. The Mg2+ increase is coupled with a decrease in ATP, which is normally bound to Mg2+ in the cell [33]. ATP inhibited Mg2+-dependent chromatin condensation in vitro. Chelating Mg2+ induced mitotic cell arrest and chromosome decondensation, while ATP reduction had the opposite effect. Our results suggest that ATP-bound Mg2+ is released by ATP hydrolysis and contributes to mitotic chromosome condensation with increased rigidity, suggesting a novel regulatory mechanism for higher-order chromatin organization by the intracellular Mg2+-ATP balance. How the negatively charged long genomic DNA is organized into mitotic chromosome remains unclear. Using a newly developed Mg2+ indicator, Maeshima et al. demonstrate a transient rise in free Mg2+ released from ATP-Mg during mitosis and suggest that the rise contributes to mitotic chromosome condensation by charge neutralization.

リンク情報
DOI
https://doi.org/10.1016/j.cub.2017.12.035
ID情報
  • DOI : 10.1016/j.cub.2017.12.035
  • ISSN : 0960-9822
  • SCOPUS ID : 85041106049

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