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Integration of telomere sequences with the draft human genome sequence

H. C. Riethman (), Z. Xiang, S. Paul, E. Morse, X.-L. Hu, J. Flint, H.-C. Chi, D. L. Grady and R. K. Moyzis
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H. C. Riethman: The Wistar Institute
Z. Xiang: The Wistar Institute
S. Paul: The Wistar Institute
E. Morse: The Wistar Institute
X.-L. Hu: The Wistar Institute
J. Flint: Institute of Molecular Medicine, John Radcliffe Hospital
H.-C. Chi: College of Medicine, University of California
D. L. Grady: College of Medicine, University of California
R. K. Moyzis: College of Medicine, University of California

Nature, 2001, vol. 409, issue 6822, 948-951

Abstract: Abstract Telomeres are the ends of linear eukaryotic chromosomes. To ensure that no large stretches of uncharacterized DNA remain between the ends of the human working draft sequence and the ends of each chromosome, we would need to connect the sequences of the telomeres to the working draft sequence. But telomeres have an unusual DNA sequence composition and organization that makes them particularly difficult to isolate and analyse. Here we use specialized linear yeast artificial chromosome clones, each carrying a large telomere-terminal fragment of human DNA, to integrate most human telomeres with the working draft sequence. Subtelomeric sequence structure appears to vary widely, mainly as a result of large differences in subtelomeric repeat sequence abundance and organization at individual telomeres. Many subtelomeric regions appear to be gene-rich, matching both known and unknown expressed genes. This indicates that human subtelomeric regions are not simply buffers of nonfunctional ‘junk DNA’ next to the molecular telomere, but are instead functional parts of the expressed genome.

Date: 2001
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DOI: 10.1038/35057180

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