Human Molecular Genetics, Vol 8, 1373-1386, Copyright © 1999 by Oxford University Press
ZE Smith and DR Higgs
We have studied replication throughout 325 kb of the telomeric region of a
human chromosome (16p13.3) and related the findings to various aspects of
chromosome structure and function (DNA sequence organization,
nuclease-hypersensitive sites, nuclear matrix attachment sites, patterns of
methylation and gene expression). The GC-rich isochore lying adjacent to
the telomere, which contains the alpha- globin locus and many widely
expressed genes, replicates early in the cell cycle regardless of the
pattern of gene expression. In subtelomeric DNA, replication occurs later
in the cell cycle and the most telomeric region (20 kb) is late
replicating. Juxtaposition of early replicating DNA next to the telomere
causes it to replicate later in S-phase. Analysis of the timing of
replication in chromosomes with deletions, or in transgenes containing
various segments of this telomeric region, suggests that there are no
critical origins or zones that initiate replication, rather the pattern of
replication appears to be related to the underlying chromatin structure
which may restrict or facilitate access to multiple, redundant origins.
These results contrast with the pattern of replication at the human
beta-globin locus and this may similarly reflect the different chromosomal
environments containing these gene clusters.
ARTICLES
The pattern of replication at a human telomeric region (16p13.3): its relationship to chromosome structure and gene expression
MRC Molecular Haematology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.
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