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Molecular and Cellular Biology, June 2000, p. 4420-4427, Vol. 20, No. 12
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Replication Delay along FRA7H, a Common Fragile
Site on Human Chromosome 7, Leads to Chromosomal Instability
Asaf
Hellman,1
Ayelet
Rahat,1
Stephen W.
Scherer,2
Ariel
Darvasi,3
Lap-Chee
Tsui,2 and
Batsheva
Kerem1,*
Department of
Genetics,1 and Department of Ecology,
Systematics and Evolution,3 The Life Sciences
Institute, The Hebrew University, Jerusalem, Israel, and
Department of Genetics, The Hospital for Sick Children,
Toronto, Ontario, Canada2
Received 5 August 1999/Accepted 10 March 2000
Common fragile sites are specific chromosomal loci that show gaps,
breaks, or rearrangements in metaphase chromosomes under conditions
that interfere with DNA replication. The mechanism underlying the
chromosomal instability at fragile sites was hypothesized to associate
with late replication time. Here, we aimed to investigate the
replication pattern of the common fragile site FRA7H, encompassing 160 kb on the long arm of human chromosome 7. Using in situ hybridization on interphase nuclei, we revealed that the replication of this region
is initiated relatively early, before 30% of S phase is completed.
However, a high fraction (~35%) of S-phase nuclei showed allelic
asynchrony, indicating that the replication of FRA7H is accomplished at
different times in S phase. This allelic asynchrony is not the result
of a specific replication time of each FRA7H allele. Analysis of the
replication pattern of adjacent clones along FRA7H by using cell
population and two-color fluorescent in situ hybridization analyses
showed significant differences in the replication of adjacent clones,
under normal growth condition and upon aphidicolin treatment. This
pattern significantly differed from that of two nonfragile regions
which showed a coordinated replication under both conditions. These
results indicate that aphidicolin is enhancing an already existing
difference in the replication time along the FRA7H region. Based on our
replication analysis of FRA7H and on previous analysis of the common
fragile site FRA3B, we suggest that delayed replication is underlying the fragility at aphidicolin-induced common fragile sites.
*
Corresponding author. Mailing address: Department of
Genetics, The Life Sciences Institute, The Hebrew University,
Jerusalem, Israel 91904. Phone: 972-2-6585689. Fax: 972-2-6586975. E-mail: kerem{at}leonardo.ls.huji.ac.il.
Molecular and Cellular Biology, June 2000, p. 4420-4427, Vol. 20, No. 12
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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