Human centromere protein B induces translational positioning of nucleosomes on α-satellite sequences

被引:47
作者
Tanaka, Y
Tachiwana, H
Yoda, K
Masumoto, H
Okazaki, T
Kurumizaka, H
Yokoyama, S
机构
[1] Waseda Univ, Grad Sch Sci & Engn, Dept Elect Engn & Biosci, Shinjuku Ku, Tokyo 1698555, Japan
[2] RIKEN, Genom Sci Ctr, Prot Res Grp, Yokohama, Kanagawa 2300045, Japan
[3] Univ Tokyo, Grad Sch Sci, Dept Biochem & Biophys, Bunkyo Ku, Tokyo 1130033, Japan
[4] Nagoya Univ, Biosci Ctr, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[5] NCI, Lab Biosyst & Canc, NIH, Bethesda, MD 20892 USA
[6] Fujita Hlth Univ, Inst Comprehens Med Sci, Toyoake, Aichi 4701192, Japan
[7] RIKEN, Harima Inst, SPring 8, Sayo, Hyogo 6795148, Japan
关键词
D O I
10.1074/jbc.M509666200
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
The human centromere proteins A (CENP-A) and B (CENP-B) are the fundamental centromere components of chromosomes. CENP-A is the centromere-specific histone H3 variant, and CENP-B specifically binds a 17-base pair sequence (the CENP-B box), which appears within every other alpha-satellite DNA repeat. In the present study, we demonstrated centromere-specific nucleosome formation in vitro with recombinant proteins, including histones H2A, H2B, H4, CENP-A, and the DNA-binding domain of CENP-B. The CENP-A nucleosome wraps 147 base pairs of the alpha-satellite sequence within its nucleosome core particle, like the canonical H3 nucleosome. Surprisingly, CENP-B binds to nucleosomal DNA when the CENP-B box is wrapped within the nucleosome core particle and induces translational positioning of the nucleosome without affecting its rotational setting. This CENP-B-induced translational positioning only occurs when the CENP-B box sequence is settled in the proper rotational setting with respect to the histone octamer surface. Therefore, CENP-B may be a determinant for translational positioning of the centromere-specific nucleosomes through its binding to the nucleosomal CENP-B box.
引用
收藏
页码:41609 / 41618
页数:10
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