Centromere protein (CENP) B boxes, recognition sequences of CENP-B, appear at regular intervals in human centromeric α-satellite DNA (alphoid DNA). In this study, to determine whether information carried by the primary sequence of alphoid DNA is involved in assembly of functional human centromeres, we created four kinds of synthetic repetitive sequences: modified alphoid DNA with point mutations in all CENP-B boxes, resulting in loss of all CENP-B binding activity; unmodified alphoid DNA containing functional CENP-B boxes; and nonalphoid repetitive DNA sequences with or without functional CENP-B boxes. These four synthetic repetitive DNAs were introduced into cultured human cells (HT1080), and de novo centromere assembly was assessed using the mammalian artificial chromosome (MAC) formation assay. We found that both the CENP-B box and the alphoid DNA sequence are required for de novo MAC formation and assembly of functional centromere components such as CENP-A, CENP-C, and CENP-E. Using the chromatin immunoprecipitation assay, we found that direct assembly of CENP-A and CENP-B in cells with synthetic alphoid DNA required functional CENP-B boxes. To the best of our knowledge, this is the first reported evidence of a functional molecular link between a centromere-specific DNA sequence and centromeric chromatin assembly in humans.
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9 December 2002
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December 02 2002
CENP-B box is required for de novo centromere chromatin assembly on human alphoid DNA
Jun-ichirou Ohzeki,
Jun-ichirou Ohzeki
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
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Megumi Nakano,
Megumi Nakano
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
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Teruaki Okada,
Teruaki Okada
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
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Hiroshi Masumoto
Hiroshi Masumoto
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
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Jun-ichirou Ohzeki
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
Megumi Nakano
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
Teruaki Okada
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
Hiroshi Masumoto
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
Address correspondence to Hiroshi Masumoto, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya 464-8602, Japan. Tel.: 81-52-789-2985. Fax: 81-52-789-5732. E-mail: [email protected]
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Abbreviations used in this paper: BAC, bacterial artificial chromosome; CENP, centromere protein; CHIP, chromatin immunoprecipitation; MAC, mammalian artificial chromosome; MTR, mutant α21-I 11mer repeat; WTR, wild-type α21-I 11mer repeat; YAC, yeast artificial chromosome.
Received:
July 22 2002
Revision Received:
October 25 2002
Accepted:
October 25 2002
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2002
J Cell Biol (2002) 159 (5): 765–775.
Article history
Received:
July 22 2002
Revision Received:
October 25 2002
Accepted:
October 25 2002
Citation
Jun-ichirou Ohzeki, Megumi Nakano, Teruaki Okada, Hiroshi Masumoto; CENP-B box is required for de novo centromere chromatin assembly on human alphoid DNA . J Cell Biol 9 December 2002; 159 (5): 765–775. doi: https://doi.org/10.1083/jcb.200207112
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