核小体
连接器DNA
组蛋白
组蛋白八聚体
染色体
组蛋白甲基化
组蛋白密码
组蛋白H2A
组蛋白H1
染色质
生物
组蛋白H3
生物物理学
遗传学
DNA
化学
细胞生物学
生物化学
DNA甲基化
基因
基因表达
作者
Amit Thakar,Pooja Gupta,Toyotaka Ishibashi,Ron M. Finn,Begonia Silva‐Moreno,Susumu Uchiyama,Kiichi Fukui,Miroslav Tomschik,Juan Ausió,Jordanka Zlatanova
出处
期刊:Biochemistry
[American Chemical Society]
日期:2009-10-30
卷期号:48 (46): 10852-10857
被引量:94
摘要
Histone variants play important roles in regulation of chromatin structure and function. To understand the structural role played by histone variants H2A.Z and H3.3, both of which are implicated in transcription regulation, we conducted extensive biochemical and biophysical analysis on mononucleosomes reconstituted from either random-sequence DNA derived from native nucleosomes or a defined DNA nucleosome positioning sequence and recombinant human histones. Using established electrophoretic and sedimentation analysis methods, we compared the properties of nucleosomes containing canonical histones and histone variants H2A.Z and H3.3 (in isolation or in combination). We find only subtle differences in the compaction and stability of the particles. Interestingly, both H2A.Z and H3.3 affect nucleosome positioning, either creating new positions or altering the relative occupancy of the existing nucleosome position space. On the other hand, only H2A.Z-containing nucleosomes exhibit altered linker histone binding. These properties could be physiologically significant as nucleosome positions and linker histone binding partly determine factor binding accessibility.
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