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Visualizing the dynamics of chromosome structure formation coupled with DNA replication
被引:18
作者:
Gotoh, Eisuke
机构:
[1] Natl Inst Infect Dis, Div Genet Resources, Shinjuku Ku, Tokyo 1628640, Japan
[2] Jikei Univ, Sch Med, Dept Radiol, Minato Ku, Tokyo 116, Japan
来源:
关键词:
D O I:
10.1007/s00412-007-0109-5
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:
A basic question of cell biology is how DNA folds to chromosome. Numbers of examples have suggested the involvement of DNA replication in chromosome structure formation. To visualize and identify the dynamics of chromosome structure formation and to elucidate the involvement of DNA replication in chromosome construction, Cy3-2'-deoxyuridine-5'-triphosphate direct-labeled active replicating DNA was observed in prematurely condensed chromosomes (PCCs) under a confocal scanning microscope utilized with drug-induced premature chromosome condensation (PCC) technique that facilitates the visualization of interphase chromatin as condensed chromosome form. S-phase PCCs revealed clearly the drastic dynamics of chromosome formation that transits during S-phase from a 'cloudy nebula' to numerous numbers of 'beads on a string' and finally to 'striped arrays of banding structured chromosome' along with the progress of DNA replication. The number, distribution, and shape of replication foci were also measured in individual subphases of S-phase more precisely than reported previously; maximally, similar to 1,400 foci of 0.35 mu m average radius size were scored at the beginning of the S-phase, and the number reduced to similar to 100 at the end of the S-phase. Drug-induced PCC clearly provided the new insight that eukaryote DNA replication is tightly coupled with the chromosome condensation/compaction for the construction of the higher-ordered structure of the eukaryote chromosome.
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页码:453 / 462
页数:10
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