化学
生物化学
染色质
组蛋白
四聚体
酶
生物
细胞生物学
DNA
作者
Narsis Attar,Oscar A. Campos,Maria Vogelauer,Chen Cheng,Yong Xue,Stefan Schmollinger,Łukasz Salwiński,Nathan V. Mallipeddi,Brandon A. Boone,Linda Yen,Sichen Yang,Shannon Zikovich,Jade Dardine,Michael Carey,Sabeeha Merchant,Siavash K. Kurdistani
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-07-02
卷期号:369 (6499): 59-64
被引量:92
标识
DOI:10.1126/science.aba8740
摘要
Enzymatic activity of histones Eukaryotic histones serve as structural elements to package DNA. However, they contain a copper-binding site for which the biological relevance is unknown. Copper homeostasis is critical for several fundamental eukaryotic processes, including mitochondrial respiration. Attar et al. hypothesized that histones may play a critical role in cellular copper utilization (see the Perspective by Rudolph and Luger). Using a multifaceted approach ranging from in vitro biochemistry to in vivo genetic and molecular analyses, they found that the histone H3-H4 tetramer is an oxidoreductase enzyme that catalyzes reduction of cupric ions, thereby providing biologically usable cuprous ions for various cellular processes. This work opens a new front for chromatin biology, with implications for eukaryotic evolution and human biology and disease. Science , this issue p. 59 ; see also p. 33
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