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M. K. Raghuraman,1*Elizabeth A. Winzeler,3*David Collingwood,2*Sonia Hunt,1Lisa Wodicka,4Andrew Conway,5David J. Lockhart,4§Ronald W. Davis,6Bonita J. Brewer,1Walton L. Fangman1
Oligonucleotide microarrays were used to map the detailed
topography of chromosome replication in the budding yeast
Saccharomycescerevisiae. The times of replication of
thousands of sites acrossthe genome were determined by hybridizing
replicated and unreplicatedDNAs, isolated at different times in S
phase, to the microarrays.Origin activations take place continuously
throughout S phasebut with most firings near mid-S phase.
Rates of replication forkmovement vary greatly from region to region
in the genome. Thetwo ends of each of the 16 chromosomes are highly
correlated intheir times of replication. This microarray approach is
readilyapplicable to other organisms, including humans.
1 Department of Genetics,
2 Department of Mathematics, University of
Washington, Seattle, WA 98195, USA.
3 Genomics
Institute of the Novartis Research Foundation, 3115 Merryfield Row, San
Diego, CA 92121, USA.
4 Affymetrix, 3380 Central
Expressway, Santa Clara, CA, USA.
5 Silicon
Genetics, 935 Washington Street, San Carlos, CA 94070, USA.
6 Department of Biochemistry, Stanford University
School of Medicine, Stanford, CA 94305, USA.
*
These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail:
raghu{at}u.washington.edu
Present address: Aventa Biosciences, 4757 Nexus
Centre Drive, Suite 200, San Diego, CA 92121, USA.
§
Present address: The Salk Institute for Biological
Studies, Laboratory of Genetics, 10010 North Torrey Pines Road, La
Jolla,CA 92037, USA.
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[DOI: 10.1126/science.294.5540.81] |Summary »|PDF »
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