When Xenopus eggs and egg extracts replicate DNA, replication origins are positioned randomly with respect to DNA sequence. However, a completely random distribution of origins would generate some unacceptably large interorigin distances. We have investigated the distribution of replication origins in Xenopus sperm nuclei replicating in Xenopus egg extract. Replicating DNA was labeled with [3H]thymidine or bromodeoxyuridine and the geometry of labeled sites on spread DNA was examined. Most origins were spaced 5–15 kb apart. This regular distribution provides an explanation for how complete chromosome replication can be ensured although origins are positioned randomly with respect to DNA sequence. Origins were grouped into small clusters (typically containing 5–10 replicons) that fired at approximately the same time, with different clusters being activated at different times in S phase. This suggests that a temporal program of origin firing similar to that seen in somatic cells also exists in the Xenopus embryo. When the quantity of origin recognition complexes (ORCs) on the chromatin was restricted, the average interorigin distance increased, and the number of origins in each cluster decreased. This suggests that the binding of ORCs to chromatin determines the regular spacing of origins in this system.
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8 January 2001
Article|
January 08 2001
Replication Origins in XenopusEgg Extract Are 5–15 Kilobases Apart and Are Activated in Clusters That Fire at Different Times
J. Julian Blow,
J. Julian Blow
aCancer Research Campaign, Chromosome Replication Research Group, Department of Biochemistry, University of Dundee, Dundee DD1 5EH, United Kingdom
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Peter J. Gillespie,
Peter J. Gillespie
aCancer Research Campaign, Chromosome Replication Research Group, Department of Biochemistry, University of Dundee, Dundee DD1 5EH, United Kingdom
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Dennis Francis,
Dennis Francis
bSchool of Biosciences, Cardiff University, Cardiff CF1 3TL, United Kingdom
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Dean A. Jackson
Dean A. Jackson
cUniversity of Manchester Institute of Science and Technology, Department of Biomolecular Sciences, Manchester M60 1QD, United Kingdom
dSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom
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J. Julian Blow
aCancer Research Campaign, Chromosome Replication Research Group, Department of Biochemistry, University of Dundee, Dundee DD1 5EH, United Kingdom
Peter J. Gillespie
aCancer Research Campaign, Chromosome Replication Research Group, Department of Biochemistry, University of Dundee, Dundee DD1 5EH, United Kingdom
Dennis Francis
bSchool of Biosciences, Cardiff University, Cardiff CF1 3TL, United Kingdom
Dean A. Jackson
cUniversity of Manchester Institute of Science and Technology, Department of Biomolecular Sciences, Manchester M60 1QD, United Kingdom
dSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom
Abbreviations used in this paper: BrdUTP, BrdU triphosphate; DIRVISH, direct visual hybridization; DMAP, dimethylaminopurine; ORC, origin recognition complex; XORC, Xenopus ORC.
Received:
October 12 2000
Revision Requested:
November 16 2000
Accepted:
November 17 2000
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Cell Biol (2001) 152 (1): 15–26.
Article history
Received:
October 12 2000
Revision Requested:
November 16 2000
Accepted:
November 17 2000
Citation
J. Julian Blow, Peter J. Gillespie, Dennis Francis, Dean A. Jackson; Replication Origins in XenopusEgg Extract Are 5–15 Kilobases Apart and Are Activated in Clusters That Fire at Different Times. J Cell Biol 8 January 2001; 152 (1): 15–26. doi: https://doi.org/10.1083/jcb.152.1.15
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