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Identification of cis-acting sites for condensin loading onto budding yeast chromosomes
被引:255
作者:
D'Ambrosio, Claudio
[1
]
Schmidt, Christine Katrin
[1
]
Katou, Yuki
[2
]
Kelly, Gavin
[3
]
Itoh, Takehiko
[4
]
Shirahige, Katsuhiko
[2
]
Uhlmann, Frank
[1
]
机构:
[1] Canc Res UK London Res Inst, Chromosome Segregat Lab, London WC2A 3PX, England
[2] Tokyo Inst Technol, Dept Biol Sci, Lab Chromosome Struct & Funct, Midori Ku, Yokohama 2268501, Japan
[3] Canc Res UK London Res Inst, Bioinformat & Biostat Serv, London WC2A 3PX, England
[4] Mitsubishi Res Inst Inc, Adv Sci & Technol Res Ctr, Chiyoda Ku, Tokyo 1008141, Japan
关键词:
chromosome condensation;
condensin;
Scc2/4;
tRNA genes;
TFIIIC;
D O I:
10.1101/gad.1675708
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Eukaryotic chromosomes reach their stable rod-shaped appearance in mitosis in a reaction dependent on the evolutionarily conserved condensin complex. Little is known about how and where condensin associates with chromosomes. Here, we analyze condensin binding to budding yeast chromosomes using high-resolution oligonucleotide tiling arrays. Condensin-binding sites coincide with those of the loading factor Scc2/4 of the related cohesin complex. The sites map to tRNA and other genes bound by the RNA polymerase III transcription factor TFIIIC, and ribosomal protein and SNR genes. An ectopic B-box element, recognized by TFIIIC, constitutes a minimal condensin-binding site, and TFIIIC and the Scc2/4 complex promote functional condensin association with chromosomes. A similar pattern of condensin binding is conserved along fission yeast chromosomes. This reveals that TFIIIC-binding sites, including tRNA genes, constitute a hitherto unknown chromosomal feature with important implications for chromosome architecture during both interphase and mitosis.
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页码:2215 / 2227
页数:13
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