Chickens possess centromeres with both extended tandem repeats and short non-tandem-repetitive sequences
- Wei-Hao Shang1,6,
- Tetsuya Hori1,6,
- Atsushi Toyoda2,
- Jun Kato3,
- Kris Popendorf4,
- Yasubumi Sakakibara4,
- Asao Fujiyama2,5 and
- Tatsuo Fukagawa1,7
- 1 Department of Molecular Genetics, National Institute of Genetics and The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka 411-8540, Japan;
- 2 Laboratory of Comparative Genomics, National Institute of Genetics and The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka 411-8540, Japan;
- 3 Department of Chemistry and Life Science, College of Bioresource Sciences, Nihon University, Kameino, Fujisawa 252-8510, Japan;
- 4 Department of Biosciences and Informatics, Keio University, Kohoku-ku, Yokohama 223-8522, Japan;
- 5 National Institute of Informatics, Hitotsubashi, Chiyoda-ku, Tokyo 101-8430, Japan
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↵6 These authors contributed equally to this work.
Abstract
The centromere is essential for faithful chromosome segregation by providing the site for kinetochore assembly. Although the role of the centromere is conserved throughout evolution, the DNA sequences associated with centromere regions are highly divergent among species and it remains to be determined how centromere DNA directs kinetochore formation. Despite the active use of chicken DT40 cells in studies of chromosome segregation, the sequence of the chicken centromere was unclear. Here, we performed a comprehensive analysis of chicken centromere DNA which revealed unique features of chicken centromeres compared with previously studied vertebrates. Centromere DNA sequences from the chicken macrochromosomes, with the exception of chromosome 5, contain chromosome-specific homogenous tandem repetitive arrays that span several hundred kilobases. In contrast, the centromeres of chromosomes 5, 27, and Z do not contain tandem repetitive sequences and span non-tandem-repetitive sequences of only ∼30 kb. To test the function of these centromere sequences, we conditionally removed the centromere from the Z chromosome using genetic engineering and have shown that that the non-tandem-repeat sequence of chromosome Z is a functional centromere.
Footnotes
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↵7 Corresponding author.
E-mail tfukagaw{at}lab.nig.ac.jp; fax 81-55-981-6742.
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[Supplemental material is available online at http://www.genome.org. The sequence data from this study have been submitted to GenBank (http://www.ncbi.nlm.nih.gov/Genbank) under accession nos. AB556430–AB556736.]
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Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.106245.110.
- Received February 5, 2010.
- Accepted June 3, 2010.
- Copyright © 2010 by Cold Spring Harbor Laboratory Press