An optimized set of human telomere clones for studying telomere integrity and architecture

被引:240
作者
Knight, SJL
Lese, CM
Precht, KS
Kuc, J
Ning, Y
Lucas, S
Regan, R
Brenan, M
Nicod, A
Lawrie, NM
Cardy, DLN
Nguyen, H
Hudson, TJ
Riethman, HC
Ledbetter, DH
Flint, J [1 ]
机构
[1] John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
[2] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[3] George Washington Univ, Washington, DC USA
[4] Gene Care Med Genet Ctr, Washington, DC USA
[5] Cytocell Ltd, Adderbury, Oxon, England
[6] MIT, Whitehead Inst Biomed Res, Ctr Genome Res, Cambridge, MA USA
[7] McGill Univ, Ctr Hlth, Montreal Genome Ctr, Montreal, PQ, Canada
[8] Wistar Inst, Philadelphia, PA 19104 USA
基金
英国惠康基金;
关键词
D O I
10.1086/302998
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Telomere-specific clones are a valuable resource for the characterization of chromosomal rearrangements. We previously reported a first-generation set of human telomere probes consisting of 34 genomic clones, which were a known distance from the end of the chromosome (similar to 300 kb), and 7 clones corresponding to the most distal markers on the integrated genetic/physical map (1p, 5p, 6p, 9p, 12p, 15q, and 20q). Subsequently, this resource has been optimized and completed: the size of the genomic clones has been expanded to a target size of 100-200 kb, which is optimal for use in genome-scanning methodologies, and additional probes for the remaining seven telomeres have been identified. For each clone we give an associated mapped sequence-tagged site and provide distances from the telomere estimated using a combination of fiberFISH, interphase FISH, sequence analysis, and radiation-hybrid mapping. This updated set of telomeric clones is an invaluable resource for clinical diagnosis and represents an important contribution to genetic and physical mapping efforts aimed at telomeric regions.
引用
收藏
页码:320 / 332
页数:13
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