Human Molecular Genetics, Vol 7, 755-761, Copyright © 1998 by Oxford University Press
MM Le Beau, FV Rassool, ME Neilly, R Espinosa 3rd, TW Glover, DI Smith and TW McKeithan
The FRA3B at 3p14.2 is the most highly expressed of the common fragile
sites observed when DNA replication is perturbed by aphidicolin or folate
stress. The molecular basis for chromosome fragility at FRA3B is unknown.
In contrast to the rare fragile sites, including FRAXA, no repeat motifs,
such as trinucleotide repeats, have been identified within FRA3B. Several
lines of evidence suggest that fragile sites are regions of DNA whose
replication is unusually sensitive to interference. We have used
fluorescence in situ hybridization to determine the relative timing of
replication of FRA3B sequences. Our studies revealed that FRA3B sequences
are late replicating. Exposure to aphidicolin, an inhibitor of both DNA
polymerase alpha and delta, results in a reproducible delay in the timing
of replication, and some cells enter G2without having completed replication
of FRA3B sequences. Our results support a model in which common fragile
sites are sequences that initiate replication late in S phase or are slow
to replicate, and the chromosomal breaks and gaps observed in metaphase
cells are due to unreplicated DNA.
ARTICLES
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction
Section of Hematology/Oncology, University of Chicago, Chicago, IL 60637, USA. mmlebeau@mcis.bsd.uchicago.edu
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